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Cor Cremers

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TOP 3
Hubert T Faber; Cor W R J Cremers; Maarten J F de Wolf; Ad F M Snik; Myrthe K S Hol
Benefit of Baha in the elderly with single-sided deafness.
Hubert T Faber; Cor W R J Cremers; Catharina A J Dun; Emmanuel A M Mylanus; Rik C Nelissen; Myrthe K S Hol
Bone-anchored hearing implant loading at 3 weeks: stability and tolerability after 6 months.
Hubert T Faber; Cor W R J Cremers; Maarten J F de Wolf; Hanneke Kievit; Ad F M Snik; Myrthe K S Hol
Analysis of factors predicting the success of the bone conduction device headband trial in patients with single-sided deafness.

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2013: Hubert T Faber; Cor W R J Cremers; Maarten J F de Wolf; Ad F M Snik; Myrthe K S Hol
Benefit of Baha in the elderly with single-sided deafness.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2013;270(4):1285-91.
2013: Hubert T Faber; Cor W R J Cremers; Catharina A J Dun; Emmanuel A M Mylanus; Rik C Nelissen; Myrthe K S Hol
Bone-anchored hearing implant loading at 3 weeks: stability and tolerability after 6 months.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2013;34(1):104-10.
2012: Hubert T Faber; Cor W R J Cremers; Maarten J F de Wolf; Hanneke Kievit; Ad F M Snik; Myrthe K S Hol
Analysis of factors predicting the success of the bone conduction device headband trial in patients with single-sided deafness.
Archives of otolaryngology--head & neck surgery 2012;138(12):1129-35.
2012: Jef J S Mulder; Jacobus J van Overbeeke; Johannes H Kaanders; Cor W R J Cremers
Radiation therapy for vestibular schwannomas.
Current opinion in otolaryngology & head and neck surgery 2012;20(5):367-71.
2012: Laura Horstink; Cor W R J Cremers; Maarten J F de Wolf; Catharina A J Dun; Hubert T Faber; Myrthe K S Hol
Titanium fixtures for bone-conduction devices and the influence of type 2 diabetes mellitus.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2012;33(6):1013-7.
2012: Henricus G X M Thomeer; Henricus P M Kunst; Cor W R J Cremers
Congenital ossicular chain anomalies associated with a mobile stapes footplate: surgical results for 23 ears.
The Annals of otology, rhinology, and laryngology 2012;121(4):275-81.
2012: Veronique J O Verhaegen; Cor W R J Cremers; Jef J S Mulder; Ad F M Snik
Application of active middle ear implants in patients with severe mixed hearing loss.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2012;33(3):297-301.
2012: Dion F Eijkenboom; Cor W R J Cremers; Berit M Verbist; Henricus P M Kunst
Bilateral conductive hearing impairment with hyperostosis of the temporal bone: a new finding in Robinow syndrome.
Archives of otolaryngology--head & neck surgery 2012;138(3):309-12.
2012: Freya K R Swinnen; Stefan Goemaere; Paul J Coucke; Cor W R J Cremers; Els M R De Leenheer; Ingeborg Dhooge
Association between bone mineral density and hearing loss in osteogenesis imperfecta.
The Laryngoscope 2012;122(2):401-8.
2012: Catharina A J Dun; Hubert T Faber; Cor W R J Cremers; Maarten J F de Wolf; Emmanuel A M Mylanus; Myrthe K S Hol
Assessment of more than 1,000 implanted percutaneous bone conduction devices: skin reactions and implant survival.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2012;33(2):192-8.
2012: Freya K R Swinnen; Francesco Zardo; Paul J Coucke; Cor W R J Cremers; Patrizia D'Eufemia; Ingeborg J M Dhooge; Ton J T M Garretsen; Els M R De Leenheer
Audiologic phenotype of osteogenesis imperfecta: use in clinical differentiation.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2012;33(2):115-22.
2012: Anne-Martine R de Heer; Patrick L M Huygen; Janneke A E Kammeraad; Saumil N Merchant; Johannes R M Cruysberg; Cor W R J Cremers
Clinical follow-up and histopathology of the temporal bones in Nathalie syndrome.
Audiology & neuro-otology 2012;17(4):219-27.
2012: Freya K R Swinnen; Paul J Coucke; Cor W R J Cremers; Els M R De Leenheer; Ingeborg Dhooge
Stapes surgery in osteogenesis imperfecta: retrospective analysis of 34 operated ears.
Audiology & neuro-otology 2012;17(3):198-206.
2011: Ferdinand C A Timmer; Jef J S Mulder; Janneke C J M Artz; Andy J Beynon; Cor W R J Cremers; Rogier T Donders; Kees Graamans
Prediction of vestibular schwannoma growth: a novel rule based on clinical symptomatology.
The Annals of otology, rhinology, and laryngology 2011;120(12):807-13.
2011: Nicole J D Weegerink; Jaap Oostrik; Ronald J E Pennings; Margit Schraders; Tim M Strom; Hanka Venselaar; Ronald J C Admiraal; Cor W R J Cremers; Mariet Elting; Susanne Granneman; Lies Hoefsloot; Patrick L M Huygen; Hannie Kremer; Henricus P M Kunst
Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations.
Journal of the Association for Research in Otolaryngology : JARO 2011;12(6):753-66.
2011: Ferdinand C A Timmer; JJ van Overbeeke; Cor W R J Cremers; Rogier T Donders; Patrick E J Hanssens; Jef J S Mulder; Kees Graamans
Gamma knife radiosurgery for vestibular schwannomas: identification of predictors for continued tumor growth and the influence of documented tumor growth preceding radiation treatment.
The Laryngoscope 2011;121(9):1834-8.
2011: Henricus G X M Thomeer; Henricus P M Kunst; Cor W R J Cremers
Congenital stapes ankylosis associated with another ossicular chain anomaly: surgical results in 30 ears.
Archives of otolaryngology--head & neck surgery 2011;137(9):935-41.
2011: Ferdinand C A Timmer; Anniek E van Haren; JJ van Overbeeke; Cor W R J Cremers; Patrick E J Hanssens; Jef J S Mulder; Kees Graamans
Follow-up after gamma knife radiosurgery for vestibular schwannomas: volumetric and axial control rates.
The Laryngoscope 2011;121(7):1359-66.
2011: Robert J Pauw; Patrick Huygen; Gordon M Colditz; Cor W R J Cremers
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
The Annals of otology, rhinology, and laryngology 2011;120(6):414-21.
2011: Catharina A J Dun; Myrthe K S Hol; Emmanuel A M Mylanus; Cor W R J Cremers
Fitting of an 8.5-millimeter abutment for bone conduction devices: indications and postintervention course.
The Annals of otology, rhinology, and laryngology 2011;120(6):386-90.
2011: Anne-Martine R de Heer; Margit Schraders; Jaap Oostrik; Lies Hoefsloot; Patrick Huygen; Cor W R J Cremers
Audioprofile-directed successful mutation analysis in a DFNA2/KCNQ4 (p.Leu274His) family.
The Annals of otology, rhinology, and laryngology 2011;120(4):243-8.
2011: Nicole J D Weegerink; Isabelle Schrauwen; Patrick Huygen; Ronald J E Pennings; Cor W R J Cremers; Guy Van Camp; Henricus P M Kunst
Phenotype of the first otosclerosis family linked to OTSC10.
The Laryngoscope 2011;121(4):838-45.
2011: Nicole J D Weegerink; Ronald J E Pennings; Patrick Huygen; Lies Hoefsloot; Cor W R J Cremers; Henricus P M Kunst
Phenotypes of two Dutch DFNA3 families with mutations in GJB2.
The Annals of otology, rhinology, and laryngology 2011;120(3):191-7.
2011: Maarten J F de Wolf; Sander Hendrix; Cor W R J Cremers; Ad F M Snik
Better performance with bone-anchored hearing aid than acoustic devices in patients with severe air-bone gap.
The Laryngoscope 2011;121(3):613-6.
2011: Maarten J F de Wolf; Myrthe K S Hol; Emmanuel A M Mylanus; Ad F M Snik; Cor W R J Cremers
Benefit and quality of life after bone-anchored hearing aid fitting in children with unilateral or bilateral hearing impairment.
Archives of otolaryngology--head & neck surgery 2011;137(2):130-8.
2011: Martijn J H Agterberg; Ad F M Snik; Myrthe K S Hol; Thamar E M van Esch; Cor W R J Cremers; Marc van Wanrooij; A John Van Opstal
Improved horizontal directional hearing in bone conduction device users with acquired unilateral conductive hearing loss.
Journal of the Association for Research in Otolaryngology : JARO 2011;12(1):1-11.
2011: Henricus P M Kunst; Martijn H Rutten; Jan-Pieter de Mönnink; Lies Hoefsloot; Henri J L M Timmers; Henri A M Marres; Jeroen C Jansen; Hannie Kremer; Jean-Pierre Bayley; Cor W R J Cremers
SDHAF2 (PGL2-SDH5) and hereditary head and neck paraganglioma.
Clinical cancer research : an official journal of the American Association for Cancer Research 2011;17(2):247-54.
2011: Martijn J H Agterberg; Myrthe K S Hol; Cor W R J Cremers; Emmanuel A M Mylanus; John van Opstal; Ad F M Snik
Conductive hearing loss and bone conduction devices: restored binaural hearing?
Advances in oto-rhino-laryngology 2011;71():84-91.
2011: Catharina A J Dun; Hubert T Faber; Maarten J F de Wolf; Cor W R J Cremers; Myrthe K S Hol
An overview of different systems: the bone-anchored hearing aid.
Advances in oto-rhino-laryngology 2011;71():22-31.
2011: Anne-Martine R de Heer; Rob W J Collin; Patrick Huygen; Margit Schraders; Jaap Oostrik; Myrthe Rouwette; Henricus P M Kunst; Hannie Kremer; Cor W R J Cremers
Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1.
Audiology & neuro-otology 2011;16(2):93-105.
2010: Henricus G X M Thomeer; Tom T H Crins; Erik J Kamsteeg; Wendy Buijsman; Johannes R M Cruysberg; Nine V A M Knoers; Cor W R J Cremers
Clinical presentation and the presence of hearing impairment in branchio-oculo-facial syndrome: a new mutation in the TFAP2A gene.
The Annals of otology, rhinology, and laryngology 2010;119(12):806-14.
2010: Veronique J O Verhaegen; Jef J S Mulder; John F P Noten; Bart M A Luijten; Cor W R J Cremers; Ad F M Snik
Intraoperative auditory steady state response measurements during Vibrant Soundbridge middle ear implantation in patients with mixed hearing loss: preliminary results.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2010;31(9):1365-8.
2010: Henricus G X M Thomeer; Henricus P M Kunst; Cor W R J Cremers
Isolated congenital stapes ankylosis: surgical results in a consecutive series of 39 ears.
The Annals of otology, rhinology, and laryngology 2010;119(11):761-6.
2010: Cor W R J Cremers; Alec Fitzgerald O'Connor; Jan Helms; Joseph Roberson; Pedro Clarós; Henning Frenzel; Milan Profant; Sébastien Schmerber; Christian Streitberger; Wolf-Dieter Baumgartner; Daniel Orfila; Mike Pringle; Carlos Cenjor; Nadia Giarbini; Dan Jiang; Ad F M Snik
International consensus on Vibrant Soundbridge® implantation in children and adolescents.
International journal of pediatric otorhinolaryngology 2010;74(11):1267-9.
2010: Myrthe K S Hol; Sylvia J W Kunst; Ad F M Snik; Arjan J Bosman; Emmanuel A M Mylanus; Cor W R J Cremers
Bone-anchored hearing aids in patients with acquired and congenital unilateral inner ear deafness (Baha CROS): clinical evaluation of 56 cases.
The Annals of otology, rhinology, and laryngology 2010;119(7):447-54.
2010: Maarten J F de Wolf; My-Linh C Shival; Myrthe K S Hol; Emmanuel A M Mylanus; Cor W R J Cremers; Ad F M Snik
Benefit and quality of life in older bone-anchored hearing aid users.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2010;31(5):766-72.
2010: Catharina A J Dun; Maarten J F de Wolf; Emmanuel A M Mylanus; Ad F M Snik; Myrthe K S Hol; Cor W R J Cremers
Bilateral bone-anchored hearing aid application in children: the Nijmegen experience from 1996 to 2008.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2010;31(4):615-23.
2010: Margit Schraders; Jaap Oostrik; Patrick Huygen; Tim M Strom; Erwin van Wijk; Henricus P M Kunst; Lies Hoefsloot; Cor W R J Cremers; Ronald J C Admiraal; Hannie Kremer
Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.
American journal of human genetics 2010;86(4):604-10.
2010: Jean-Pierre Bayley; Henricus P M Kunst; Alberto Cascon; Maria Lourdes Sampietro; José Gaal; Esther Korpershoek; Adolfo Hinojar-Gutierrez; Henri J L M Timmers; Lies Hoefsloot; Mario A Hermsen; Carlos Suárez; A Karim Hussain; Annette H J T Vriends; Frederik J Hes; Jeroen C Jansen; Carli M Tops; Eleonora P Corssmit; Peter de Knijff; Jacques W M Lenders; Cor W R J Cremers; Peter Devilee; Winand N M Dinjens; Ronald R de Krijger; Mercedes Robledo
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.
The lancet oncology 2010;11(4):366-72.
2010: Margit Schraders; Kwanghyuk Lee; Jaap Oostrik; Patrick Huygen; Ghazanfar Ali; Lies Hoefsloot; Joris Veltman; Frans P M Cremers; Sulman Basit; Muhammad Ansar; Cor W R J Cremers; Henricus P M Kunst; Wasim Ahmad; Ronald J C Admiraal; Suzanne M Leal; Hannie Kremer
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.
American journal of human genetics 2010;86(2):138-47.
2010: Barend F T Hogewind; Ronald J E Pennings; Frans A Hol; Henricus P M Kunst; Lies Hoefsloot; Johannes R M Cruysberg; Cor W R J Cremers
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.
Molecular vision 2010;16():26-35.
2009: Isabelle Schrauwen; Melissa Thys; Kathleen Vanderstraeten; Erik Fransen; Megan Ealy; Cor W R J Cremers; Ingeborg Dhooge; Paul Van de Heyning; Erwin Offeciers; Richard J H Smith; Guy Van Camp
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch population.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2009;30(8):1079-83.
2009: Veronique J O Verhaegen; Jef J S Mulder; Emmanuel A M Mylanus; Cor W R J Cremers; Ad F M Snik
Profound mixed hearing loss: bone-anchored hearing aid system or cochlear implant?
The Annals of otology, rhinology, and laryngology 2009;118(10):693-7.
2009: Maarten J F de Wolf; Joop M Leijendeckers; Emmanuel A M Mylanus; Myrthe K S Hol; Ad F M Snik; Cor W R J Cremers
Age-related use and benefit of the bone-anchored hearing aid compact.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2009;30(6):787-92.
2009: Ronald J E Pennings; Lishya Liauw; Cor W R J Cremers
A spontaneous otogenic extradural pneumocephalus.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2009;30(6):864.
2009: Huai-Xiang Hao; Oleh Khalimonchuk; Margit Schraders; Noah Dephoure; Jean-Pierre Bayley; Henricus Kunst; Peter Devilee; Cor W R J Cremers; Joshua Schiffman; Brandon G Bentz; Steven P Gygi; Dennis R Winge; Hannie Kremer; Jared Rutter
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.
Science (New York, N.Y.) 2009;325(5944):1139-42.
2009: Hubert T Faber; Maarten J F de Wolf; Jacky W J de Rooy; Myrthe K S Hol; Cor W R J Cremers; Emmanuel A M Mylanus
Bone-anchored hearing aid implant location in relation to skin reactions.
Archives of otolaryngology--head & neck surgery 2009;135(8):742-7.
2009: Maarten J F de Wolf; Myrthe K S Hol; Emmanuel A M Mylanus; Cor W R J Cremers
Bone-anchored hearing aid surgery in older adults: implant loss and skin reactions.
The Annals of otology, rhinology, and laryngology 2009;118(7):525-31.
2009: Ferdinand C A Timmer; Patrick E J Hanssens; Anniek E P van Haren; Jef J S Mulder; Cor W R J Cremers; Andy J Beynon; JJ van Overbeeke; Kees Graamans
Gamma knife radiosurgery for vestibular schwannomas: results of hearing preservation in relation to the cochlear radiation dose.
The Laryngoscope 2009;119(6):1076-81.
2009: Freya K R Swinnen; Els M R De Leenheer; Paul J Coucke; Cor W R J Cremers; Ingeborg J M Dhooge
Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta.
The Laryngoscope 2009;119(6):1171-9.
2009: Anne-Martine R de Heer; Patrick Huygen; Rob W J Collin; Jaap Oostrik; Hannie Kremer; Cor W R J Cremers
Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1.
The Annals of otology, rhinology, and laryngology 2009;118(5):382-90.
2009: Stijn J C van der Avoort; Niels van Heerbeek; Gerhard A Zielhuis; Cor W R J Cremers
Sonotubometry in children with otitis media with effusion before and after insertion of ventilation tubes.
Archives of otolaryngology--head & neck surgery 2009;135(5):448-52.
2009: Janneke C J M Artz; Ferdinand C A Timmer; Jef J S Mulder; Cor W R J Cremers; Kees Graamans
Predictors of future growth of sporadic vestibular schwannomas obtained by history and radiologic assessment of the tumor.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2009;266(5):641-6.
2009: Anne-Martine R de Heer; Patrick Huygen; Rob W J Collin; Hannie Kremer; Cor W R J Cremers
Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.
The Annals of otology, rhinology, and laryngology 2009;118(4):313-20.
2009: Ronald J E Pennings; Cor W R J Cremers
Postauricular approach atticotomy: a modified closed technique with reconstruction of the scutum with cymbal cartilage.
The Annals of otology, rhinology, and laryngology 2009;118(3):199-204.
2009: Isabelle Schrauwen; Megan Ealy; Matthew Huentelman; Melissa Thys; Nils Homer; Kathleen Vanderstraeten; Erik Fransen; Jason J Corneveaux; David Craig; Mireille Claustres; Cor W R J Cremers; Ingeborg Dhooge; Paul Van de Heyning; Robert Vincent; Erwin Offeciers; Richard J H Smith; Guy Van Camp
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
American journal of human genetics 2009;84(3):328-38.
2009: F J Wendy van Drunen; Robert J Pauw; Rob W J Collin; Hannie Kremer; Patrick Huygen; Cor W R J Cremers
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3.
Audiology & neuro-otology 2009;14(5):303-7.
2009: Joop M Leijendeckers; Ronald J E Pennings; Ad F M Snik; Arjan J Bosman; Cor W R J Cremers
Audiometric characteristics of USH2a patients.
Audiology & neuro-otology 2009;14(4):223-31.
2008: Maarten J F de Wolf; Myrthe K S Hol; Patrick Huygen; Emmanuel A M Mylanus; Cor W R J Cremers
Clinical outcome of the simplified surgical technique for BAHA implantation.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008;29(8):1100-8.
2008: Rob W J Collin; Anne-Martine R de Heer; Jaap Oostrik; Robert J Pauw; Rutger F Plantinga; Patrick Huygen; Ronald J C Admiraal; Arjan de Brouwer; Tim M Strom; Cor W R J Cremers; Hannie Kremer
Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer.
European journal of human genetics : EJHG 2008;16(12):1430-6.
2008: C V M Verhagen; Myrthe K S Hol; W Coppens-Schellekens; Ad F M Snik; Cor W R J Cremers
The Baha Softband. A new treatment for young children with bilateral congenital aural atresia.
International journal of pediatric otorhinolaryngology 2008;72(10):1455-9.
2008: Ad F M Snik; Joop Leijendeckers; Myrthe K S Hol; Emmanuel A M Mylanus; Cor W R J Cremers
The bone-anchored hearing aid for children: recent developments.
International journal of audiology 2008;47(9):554-9.
2008: Veronique J O Verhaegen; Emmanuel A M Mylanus; Cor W R J Cremers; Ad F M Snik
Audiological application criteria for implantable hearing aid devices: a clinical experience at the Nijmegen ORL clinic.
The Laryngoscope 2008;118(9):1645-9.
2008: Rutger F Plantinga; Ronald Pennings; Patrick Huygen; Rocco Bruno; Philipp Eller; Timothy G Barrett; Bernard Vialettes; Veronique Paquis-Fluklinger; Fortunato Lombardo; Cor W R J Cremers
Hearing impairment in genotyped Wolfram syndrome patients.
The Annals of otology, rhinology, and laryngology 2008;117(7):494-500.
2008: Stijn J C van der Avoort; Niels van Heerbeek; Ronald J C Admiraal; Gerhard A Zielhuis; Cor W R J Cremers
Results of sonotubometry in testing eustachian tube ventilatory function in children with cleft palate.
The Annals of otology, rhinology, and laryngology 2008;117(5):335-40.
2008: Sylvia J W Kunst; Myrthe K S Hol; Emmanuel A M Mylanus; Joop M Leijendeckers; Ad F M Snik; Cor W R J Cremers
Subjective benefit after BAHA system application in patients with congenital unilateral conductive hearing impairment.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008;29(3):353-58.
2008: Amit Kochhar; Dana J Orten; Jessica L Sorensen; Stephanie M Fischer; Cor W R J Cremers; William J Kimberling; Richard J H Smith
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
Human mutation 2008;29(4):565.
2008: Rob W J Collin; Ramesh Chellappa; Robert J Pauw; Gert Vriend; Jaap Oostrik; Wendy van Drunen; Patrick Huygen; Ronald J C Admiraal; Lies Hoefsloot; Frans P M Cremers; Mengqing Xiang; Cor W R J Cremers; Hannie Kremer
Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding.
Human mutation 2008;29(4):545-54.
2008: Dana J Orten; Stephanie M Fischer; Jessica L Sorensen; Uppala Radhakrishna; Cor W R J Cremers; Henri Marres; Guy Van Camp; Katherine O Welch; Richard J H Smith; William J Kimberling
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR.
Human mutation 2008;29(4):537-44.
2008: Robert J Pauw; F J Wendy van Drunen; Rob W J Collin; Patrick Huygen; Hannie Kremer; Cor W R J Cremers
Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.
Archives of otolaryngology--head & neck surgery 2008;134(3):294-300.
2008: Sylvia J W Kunst; Joop M Leijendeckers; Emmanuel A M Mylanus; Myrthe K S Hol; Ad F M Snik; Cor W R J Cremers
Bone-anchored hearing aid system application for unilateral congenital conductive hearing impairment: audiometric results.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008;29(1):2-7.
2008: Rob W J Collin; Ersan Kalay; Muhammad Tariq; Theo Peters; Bert van der Zwaag; Hanka Venselaar; Jaap Oostrik; Kwanghyuk Lee; Zubair M Ahmed; Refik Caylan; Yun Li; Henk A Spierenburg; Erol Eyupoglu; Angelien Heister; Saima Riazuddin; Elif Bahat; Muhammad Ansar; Selcuk Arslan; Bernd Wollnik; Han G Brunner; Cor W R J Cremers; Ahmet Karaguzel; Wasim Ahmad; Frans P M Cremers; Gert Vriend; Thomas B Friedman; Sheikh Amer Riazuddin; Suzanne M Leal; Hannie Kremer
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
American journal of human genetics 2008;82(1):125-38.
2007: Cor W R J Cremers
[Turner syndrome in adulthood].
Nederlands tijdschrift voor geneeskunde 2007;151(42):2353-4; author reply 2354.
2007: Ersan Kalay; Abdullah Uzumcu; Elmar Krieger; Refik Caylan; Oya Uyguner; Melike Ulubil-Emiroglu; Hidayet Erdol; Hulya Kayserili; Gunter Hafiz; Nermin Başerer; Angelien J G M Heister; Hans Christian Hennies; Peter Nürnberg; Seher Başaran; Han G Brunner; Cor W R J Cremers; Ahmet Karaguzel; Bernd Wollnik; Hannie Kremer
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.
American journal of medical genetics. Part A 2007;143A(20):2382-9.
2007: Sylvia J W Kunst; Myrthe K S Hol; Cor W R J Cremers; Emmanuel A M Mylanus
Bone-anchored hearing aid in patients with moderate mental retardation: impact and benefit assessment.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2007;28(6):793-7.
2007: Niels van Heerbeek; Stijn J C van der Avoort; Gerhard A Zielhuis; Cor W R J Cremers
Sonotubometry: a useful tool to measure intra-individual changes in eustachian tube ventilatory function.
Archives of otolaryngology--head & neck surgery 2007;133(8):763-6.
2007: Robert J Pauw; Patrick Huygen; Melissa Thys; Guy Van Camp; Frank B M Joosten; Cor W R J Cremers
Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7.
American journal of medical genetics. Part A 2007;143A(14):1613-22.
2007: Rob W J Collin; Ersan Kalay; Jaap Oostrik; Refik Caylan; Bernd Wollnik; Selçuk Arslan; Anneke I den Hollander; Yelda Birinci; Peter Lichtner; Tim M Strom; Bayram Toraman; Lies Hoefsloot; Cor W R J Cremers; Han G Brunner; Frans P M Cremers; Ahmet Karaguzel; Hannie Kremer
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.
Human mutation 2007;28(7):718-23.
2007: Ad F M Snik; Noortje T L van Duijnhoven; Jef J S Mulder; Cor W R J Cremers
Evaluation of the subjective effect of middle ear implantation in hearing-impaired patients with severe external otitis.
Journal of the American Academy of Audiology 2007;18(6):496-503.
2007: Robert J Pauw; Patrick Huygen; Rob W J Collin; J R M Cruysberg; Lies Hoefsloot; Hannie Kremer; Cor W R J Cremers
Phenotype description of a novel DFNA9/COCH mutation, I109T.
The Annals of otology, rhinology, and laryngology 2007;116(5):349-57.
2007: Anne M L C Bischoff; Robert J Pauw; Patrick Huygen; Albert L Aandekerk; Hannie Kremer; Cor W R J Cremers; J R M Cruysberg
Vertical corneal striae in families with autosomal dominant hearing loss: DFNA9/COCH.
American journal of ophthalmology 2007;143(5):847-852.
2007: Ersan Kalay; Refik Caylan; A F Kiroglu; tekin yasar; Rob W J Collin; J G A M Heister; Jaap Oostrik; Cor W R J Cremers; Han G Brunner; Ahmet Karaguzel; Hannie Kremer
A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.
Journal of molecular medicine (Berlin, Germany) 2007;85(4):397-404.
2007: Cor W R J Cremers; Rutger F Plantinga; Hannie Kremer
[From gene to disease; DFNA8/12, an autosomal dominant inherited bowl-shaped sensorineural hearing impairment].
Nederlands tijdschrift voor geneeskunde 2007;151(9):531-4.
2007: Rutger F Plantinga; Cor W R J Cremers; Patrick Huygen; Henricus P M Kunst; Arjan J Bosman
Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
Journal of the Association for Research in Otolaryngology : JARO 2007;8(1):1-7.
2007: Stijn J C van der Avoort; Niels van Heerbeek; Ad F M Snik; Gerhard A Zielhuis; Cor W R J Cremers
Reproducibility of sonotubometry as Eustachian tube ventilatory function test in healthy children.
International journal of pediatric otorhinolaryngology 2007;71(2):291-5.
2007: Frans P M Cremers; William J Kimberling; Maigi Külm; Arjan de Brouwer; Erwin van Wijk; Heleen te Brinke; Cor W R J Cremers; Lies Hoefsloot; Sandro Banfi; Francesca Simonelli; Johannes C Fleischhauer; Wolfgang Berger; Philip M Kelley; Elene Haralambous; Maria Bitner-Glindzicz; Andrew R Webster; Zubin Saihan; Elfride De Baere; Bart P Leroy; Giuliana Silvestri; Gareth J McKay; Robert K Koenekoop; Jose M Millan; Thomas Rosenberg; Tarja Joensuu; Eeva-Marja Sankila; Dominique Weil; Michael D Weston; Bernd Wissinger; Hannie Kremer
Development of a genotyping microarray for Usher syndrome.
Journal of medical genetics 2007;44(2):153-60.
2007: Robert J Pauw; Rob W J Collin; Patrick Huygen; Lies Hoefsloot; Hannie Kremer; Cor W R J Cremers
Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W.
Audiology & neuro-otology 2007;12(2):77-84.
2007: Cor W R J Cremers
How to prevent a stapes gusher.
Advances in oto-rhino-laryngology 2007;65():278-84.
2006: Ad F M Snik; Noortje T L van Duijnhoven; Emmanuel A M Mylanus; Cor W R J Cremers
Estimated cost-effectiveness of active middle-ear implantation in hearing-impaired patients with severe external otitis.
Archives of otolaryngology--head & neck surgery 2006;132(11):1210-5.
2006: Stijn J C van der Avoort; N van Heerbeek; Gerhard A Zielhuis; Cor W R J Cremers
Validation of sonotubometry in healthy adults.
The Journal of laryngology and otology 2006;120(10):853-6.
2006: Jan-Jaap Hendrickx; Aart H Mudde; Leen M 't Hart; Patrick Huygen; Cor W R J Cremers
Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2006;27(6):802-8.
2006: Rob W J Collin; Robert J Pauw; Jeroen Schoots; Patrick Huygen; Lies Hoefsloot; Cor W R J Cremers; Hannie Kremer
Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9).
American journal of medical genetics. Part A 2006;140(16):1791-4.
2006: Arjan J Bosman; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Fitting range of the BAHA Cordelle.
International journal of audiology 2006;45(8):429-37.
2006: Sylvia J W Kunst; Myrthe K S Hol; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Rehabilitation of patients with conductive hearing loss and moderate mental retardation by means of a bone-anchored hearing aid.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2006;27(5):653-8.
2006: Ersan Kalay; Yun Li; Abdullah Uzumcu; Oya Uyguner; Rob W J Collin; Refik Caylan; Melike Ulubil-Emiroglu; Ferry F J Kersten; Gunter Hafiz; Erwin van Wijk; Hulya Kayserili; Edyta Rohmann; Janine Wagenstaller; Lies Hoefsloot; Tim M Strom; Gudrun Nürnberg; Nermin Baserer; Anneke I den Hollander; Frans P M Cremers; Cor W R J Cremers; Christian Becker; Han G Brunner; Peter Nürnberg; Ahmet Karaguzel; Seher Basaran; Christian Kubisch; Hannie Kremer; Bernd Wollnik
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.
Human mutation 2006;27(7):633-9.
2006: Rutger F Plantinga; Arjan de Brouwer; Patrick Huygen; Henricus P M Kunst; Hannie Kremer; Cor W R J Cremers
A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation.
Journal of the Association for Research in Otolaryngology : JARO 2006;7(2):173-81.
2006: Ronald Pennings; Godelieve W J A Damen; Ad F M Snik; Lies Hoefsloot; Cor W R J Cremers; Emmanuel A M Mylanus
Audiologic performance and benefit of cochlear implantation in Usher syndrome type I.
The Laryngoscope 2006;116(5):717-22.
2006: Anne M L C Bischoff; Ronald Pennings; Patrick Huygen; Mirjam W J Luijendijk; Erwin van Wijk; J R M Cruysberg; Hannie Kremer; Cor W R J Cremers
Cochleovestibular and ocular features in a Dutch DFNA11 family.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2006;27(3):323-31.
2006: Robert J Pauw; Els M R De Leenheer; Kris Van Den Bogaert; Patrick Huygen; Guy Van Camp; Frank B M Joosten; Cor W R J Cremers
The phenotype of the first otosclerosis family linked to OTSC5.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2006;27(3):308-15.
2006: Edyta Rohmann; Han G Brunner; Hulya Kayserili; Oya Uyguner; Gudrun Nürnberg; Erin Lew; Angus Dobbie; Veraragavan Eswarakumar; Abdullah Uzumcu; Melike Ulubil-Emeroglu; Jules G Leroy; Yun Li; Christian Becker; Kai Lehnerdt; Cor W R J Cremers; Memnune Yüksel-Apak; Peter Nürnberg; Christian Kubisch; Chriütian Kubisch; Joseph Schlessinger; Hans van Bokhoven; Bernd Wollnik
Mutations in different components of FGF signaling in LADD syndrome.
Nature genetics 2006;38(4):414-7.
2006: Nahid G Robertson; Cor W R J Cremers; Patrick Huygen; Tetsuo Ikezono; Bryan Krastins; Hannie Kremer; Sharon F Kuo; M Charles Liberman; Saumil N Merchant; Constance E Miller; Joseph B Nadol; David A Sarracino; Wim I M Verhagen; Cynthia C Morton
Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.
Human molecular genetics 2006;15(7):1071-85.
2006: George Thomas; P G C Kooijman; Cor W R J Cremers; F I C R S de Jong
A comparative study of voice complaints and risk factors for voice complaints in female student teachers and practicing teachers early in their career.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2006;263(4):370-80.
2006: Theo A Peters; Elena N Levtchenko; Cor W R J Cremers; Jo H A J Curfs; Leo A H Monnens
No evidence of hearing loss in pseudohypoaldosteronism type 1 patients.
Acta oto-laryngologica 2006;126(3):237-9.
2006: Erwin van Wijk; Bert van der Zwaag; Theo Peters; Ulrike Zimmermann; Heleen te Brinke; Ferry F J Kersten; Tina Märker; Elena Aller; Lies Hoefsloot; Cor W R J Cremers; Frans P M Cremers; Uwe Wolfrum; Marlies Knipper; Ronald Roepman; Hannie Kremer
The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1.
Human molecular genetics 2006;15(5):751-65.
2006: Rutger F Plantinga; Ronald Pennings; Patrick Huygen; Eeva-Marja Sankila; Kaija Tuppurainen; Leenamaija Kleemola; Cor W R J Cremers; August F Deutman
Visual impairment in Finnish Usher syndrome type III.
Acta ophthalmologica Scandinavica 2006;84(1):36-41.
2006: George Thomas; F I C R S de Jong; P G C Kooijman; A Rogier T Donders; Cor W R J Cremers
Voice complaints, risk factors for voice problems and history of voice problems in relation to puberty in female student teachers.
Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP) 2006;58(5):305-22.
2006: George Thomas; F I C R S de Jong; P G C Kooijman; Cor W R J Cremers
Utility of the Type D Scale 16 and Voice Handicap Index to assist voice care in student teachers and teachers.
Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP) 2006;58(4):250-63.
2006: George Thomas; F I C R S de Jong; Cor W R J Cremers; P G C Kooijman
Prevalence of voice complaints, risk factors and impact of voice problems in female student teachers.
Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP) 2006;58(2):65-84.
2005: Ad F M Snik; Emmanuel A M Mylanus; David W Proops; John Wolfaardt; William E Hodgetts; Thomas Somers; John K Niparko; Jack J Wazen; Olivier Sterkers; Cor W R J Cremers; Anders Tjellström
Consensus statements on the BAHA system: where do we stand at present?
The Annals of otology, rhinology & laryngology. Supplement 2005;195():2-12.
2005: Ersan Kalay; Ahmet Karaguzel; Refik Caylan; A Heister; Frans P M Cremers; Cor W R J Cremers; Han G Brunner; Arjan de Brouwer; Hannie Kremer
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss.
Human mutation 2005;26(6):591.
2005: Ersan Kalay; Arjan de Brouwer; Refik Caylan; Sander B Nabuurs; Bernd Wollnik; Ahmet Karaguzel; J G A M Heister; Hidayet Erdol; Frans P M Cremers; Cor W R J Cremers; Han G Brunner; Hannie Kremer
A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome.
Journal of molecular medicine (Berlin, Germany) 2005;83(12):1025-32.
2005: Cor W R J Cremers; Martijn H Kemperman; Steven J H Bom; Patrick Huygen; Wim I M Verhagen; J M J Kremer
[From gene to disease; a progressive cochlear-vestibular dysfunction with onset in middle-age (DFNA9)].
Nederlands tijdschrift voor geneeskunde 2005;149(47):2619-21.
2005: Myrthe K S Hol; Arjan J Bosman; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Bone-anchored hearing aids in unilateral inner ear deafness: an evaluation of audiometric and patient outcome measurements.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2005;26(5):999-1006.
2005: Martijn H Kemperman; Els M R De Leenheer; Patrick Huygen; Gerard van Duijnhoven; Cynthia C Morton; Nahid G Robertson; Frans P M Cremers; Hannie Kremer; Cor W R J Cremers
Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutation.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2005;26(5):926-33.
2005: Anne M L C Bischoff; Patrick Huygen; Martijn H Kemperman; Ronald Pennings; Steven J H Bom; Wim I M Verhagen; Ronald J C Admiraal; Hannie Kremer; Cor W R J Cremers
Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2005;26(5):918-25.
2005: Arjan de Brouwer; Henricus P M Kunst; Alice Krebsova; Karin van Asseldonk; André Reis; Rikkert L Snoeckx; Guy Van Camp; Cor W R J Cremers; Frans P M Cremers; Hannie Kremer
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.
American journal of medical genetics. Part A 2005;137(1):41-6.
2005: Myrthe K S Hol; Cor W R J Cremers; Wilma Coppens-Schellekens; Ad F M Snik
The BAHA Softband. A new treatment for young children with bilateral congenital aural atresia.
International journal of pediatric otorhinolaryngology 2005;69(7):973-80.
2005: Stijn J C van der Avoort; Niels van Heerbeek; Gerhard A Zielhuis; Cor W R J Cremers
Sonotubometry: eustachian tube ventilatory function test: a state-of-the-art review.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2005;26(3):538-43; discussion 543.
2005: Myrthe K S Hol; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Does the bone-anchored hearing aid have a complementary effect on audiological and subjective outcomes in patients with unilateral conductive hearing loss?
Audiology & neuro-otology 2005;10(3):159-68.
2005: Myrthe K S Hol; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Long-term results of bone-anchored hearing aid recipients who had previously used air-conduction hearing aids.
Archives of otolaryngology--head & neck surgery 2005;131(4):321-5.
2005: Rutger F Plantinga; Leenamaija Kleemola; Patrick Huygen; Tarja Joensuu; Eeva-Marja Sankila; Ronald Pennings; Cor W R J Cremers
Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients.
Audiology & neuro-otology 2005;10(2):79-89.
2005: Regie Lyn P Santos; Yurii Aulchenko; Patrick Huygen; Kim P van der Donk; Ilse J de Wijs; Martijn H Kemperman; Ronald J C Admiraal; Hannie Kremer; Lies Hoefsloot; Cor W R J Cremers
Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations.
International journal of pediatric otorhinolaryngology 2005;69(2):165-74.
2005: Vedat Topsakal; Ronald Pennings; Heleen te Brinke; Ben Hamel; Patrick Huygen; Hannie Kremer; Cor W R J Cremers
Phenotype determination guides swift genotyping of a DFNA2/KCNQ4 family with a hot spot mutation (W276S).
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2005;26(1):52-8.
2005: Henriëtte H Weekamp; Hannie Kremer; Lies Hoefsloot; Anne Marie Kuijpers-Jagtman; J R M Cruysberg; Cor W R J Cremers
Teunissen-Cremers syndrome: a clinical, surgical, and genetic report.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2005;26(1):38-51.
2004: Laura W J Baijens; Els M R De Leenheer; Henriëtte H Weekamp; J R M Cruysberg; Geert R Mortier; Cor W R J Cremers
Stickler syndrome type I and Stapes ankylosis.
International journal of pediatric otorhinolaryngology 2004;68(12):1573-80.
2004: Els M R De Leenheer; Arjan J Bosman; Henricus P M Kunst; Patrick Huygen; Cor W R J Cremers
Audiological characteristics of some affected members of a Dutch DFNA13/COL11A2 family.
The Annals of otology, rhinology, and laryngology 2004;113(11):922-9.
2004: Theo A Peters; Leo A H Monnens; Cor W R J Cremers; Jo H A J Curfs
Genetic disorders of transporters/channels in the inner ear and their relation to the kidney.
Pediatric nephrology (Berlin, Germany) 2004;19(11):1194-201.
2004: Martijn H Kemperman; Sacha M P Koch; Shrawan Kumar; Patrick Huygen; Frank B M Joosten; Cor W R J Cremers
Evidence of progression and fluctuation of hearing impairment in branchio-oto-renal syndrome.
International journal of audiology 2004;43(9):523-32.
2004: Ronald Pennings; Vedat Topsakal; Lisa M Astuto; Arjan de Brouwer; Michiel Wagenaar; Patrick Huygen; William J Kimberling; August F Deutman; Hannie Kremer; Cor W R J Cremers
Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12).
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2004;25(5):699-706.
2004: Myrthe K S Hol; Arjan J Bosman; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Bone-anchored hearing aid in unilateral inner ear deafness: a study of 20 patients.
Audiology & neuro-otology 2004;9(5):274-81.
2004: Ronald Pennings; Heleen te Brinke; Michael D Weston; Annemarie Claassen; Dana J Orten; Henriëtte H Weekamp; Annelies van Aarem; Patrick Huygen; August F Deutman; Lies Hoefsloot; Frans P M Cremers; Cor W R J Cremers; William J Kimberling; Hannie Kremer
USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.
Human mutation 2004;24(2):185.
2004: Christel Stinckens; Hannie Kremer; Erwin van Wijk; Lies Hoefsloot; Patrick Huygen; Lieve Standaert; Jean-Pierre Fryns; Cor W R J Cremers
Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations.
The Annals of otology, rhinology, and laryngology 2004;113(7):587-93.
2004: Glen FORTON; Cor W R J Cremers; E Erwin Offeciers
Acoustic neuroma ingrowth in the cochlear nerve: does it influence the clinical presentation?
The Annals of otology, rhinology, and laryngology 2004;113(7):582-6.
2004: Mirjam W J Luijendijk; Erwin van Wijk; Anne M L C Bischoff; Elmar Krieger; Patrick Huygen; Ronald Pennings; Han G Brunner; Cor W R J Cremers; Frans P M Cremers; Hannie Kremer
Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).
Human genetics 2004;115(2):149-56.
2004: Ad F M Snik; Arjan J Bosman; Emmanuel A M Mylanus; Cor W R J Cremers
Candidacy for the bone-anchored hearing aid.
Audiology & neuro-otology 2004;9(4):190-6.
2004: Kris Van Den Bogaert; Els M R De Leenheer; Wenjie Chen; Y Lee; P Nürnberg; Ronald Pennings; Kathleen Vanderstraeten; Melissa Thys; Cor W R J Cremers; R J H Smith; Guy Van Camp
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24.
Journal of medical genetics 2004;41(6):450-3.
2004: Myrthe K S Hol; Marian A Spath; Paul Krabbe; Catharina T M van der Pouw; Ad F M Snik; Cor W R J Cremers; Emmanuel A M Mylanus
The bone-anchored hearing aid: quality-of-life assessment.
Archives of otolaryngology--head & neck surgery 2004;130(4):394-9.
2004: Ronald Pennings; Patrick Huygen; Dana J Orten; Michiel Wagenaar; Annelies van Aarem; Hannie Kremer; William J Kimberling; Cor W R J Cremers; August F Deutman
Evaluation of visual impairment in Usher syndrome 1b and Usher syndrome 2a.
Acta ophthalmologica Scandinavica 2004;82(2):131-9.
2004: Erwin van Wijk; Ronald Pennings; Heleen te Brinke; Annemarie Claassen; Helger G Yntema; Lies Hoefsloot; Frans P M Cremers; Cor W R J Cremers; Hannie Kremer
Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II.
American journal of human genetics 2004;74(4):738-44.
2004: Ad F M Snik; John Noten; Cor W R J Cremers
Gain and maximum output of two electromagnetic middle ear implants: are real ear measurements helpful?
Journal of the American Academy of Audiology 2004;15(3):249-57.
2004: Martijn H Kemperman; Els M R De Leenheer; Patrick Huygen; Erwin van Wijk; Gerard van Duijnhoven; Frans P M Cremers; Hannie Kremer; Cor W R J Cremers
A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.
Archives of otolaryngology--head & neck surgery 2004;130(3):281-8.
2004: Ad F M Snik; Cor W R J Cremers
Audiometric evaluation of an attempt to optimize the fixation of the transducer of a middle-ear implant to the ossicular chain with bone cement.
Clinical otolaryngology and allied sciences 2004;29(1):5-9.
2004: Rikkert L Snoeckx; Hannie Kremer; Robbert J H Ensink; Kris Flothmann; Arjan de Brouwer; R J H Smith; Cor W R J Cremers; Guy Van Camp
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3.
Journal of medical genetics 2004;41(1):11-3.
2004: Ronald Pennings; Patrick Huygen; Jody M W van den Ouweland; Kim Cryns; Lambert D Dikkeschei; Guy Van Camp; Cor W R J Cremers
Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.
Audiology & neuro-otology 2004;9(1):51-62.
2004: Anne M L C Bischoff; Mirjam W J Luijendijk; Patrick Huygen; Gerard van Duijnhoven; Els M R De Leenheer; Grétel G Oudesluijs; Lut Van Laer; Frans P M Cremers; Cor W R J Cremers; Hannie Kremer
A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation.
Audiology & neuro-otology 2004;9(1):34-46.
2003: Erwin van Wijk; Elmar Krieger; Martijn H Kemperman; Els M R De Leenheer; Patrick Huygen; Cor W R J Cremers; Frans P M Cremers; Hannie Kremer
A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).
Journal of medical genetics 2003;40(12):879-84.
2003: Ronald Pennings; Kim Cryns; Patrick Huygen; Guy Van Camp; Cor W R J Cremers
[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].
Nederlands tijdschrift voor geneeskunde 2003;147(44):2170-2.
2003: Inge Nuijten; Ronald J C Admiraal; Griet Van Buggenhout; Cor W R J Cremers; Jean-Pierre Frijns; Dominique Smeets; Conny van Ravenswaaij-Arts
Congenital aural atresia in 18q deletion or de Grouchy syndrome.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(6):900-6.
2003: Kim Cryns; Theru A Sivakumaran; Jody M W van den Ouweland; Ronald Pennings; Cor W R J Cremers; Kris Flothmann; Terry-Lynn Young; Richard J H Smith; Marci M Lesperance; Guy Van Camp
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.
Human mutation 2003;22(4):275-87.
2003: Francois X Lemaire; Louw Feenstra; Patrick Huygen; Erik Fransen; koenraad devriendt; Guy Van Camp; Greet Vantrappen; Cor W R J Cremers; P Ashley Wackym; John C Koss
Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo (DFNA9/COCH): longitudinal analyses in a belgian family.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(5):743-8.
2003: Henriëtte H Weekamp; Patrick Huygen; J L Merx; H P H Kremer; Cor W R J Cremers; Neil S Longridge
Longitudinal analysis of hearing loss in a case of hemosiderosis of the central nervous system.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(5):738-42.
2003: Antoon J M van der Rijt; Cor W R J Cremers
Stapes surgery in osteogenesis imperfecta: results of a new series.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(5):717-22.
2003: Robbert J H Ensink; H M Vingerhoets; C W Thijs H Schmidt; Cor W R J Cremers
Treatment for severe palatoclonus by occlusion of the eustachian tube.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(5):714-6.
2003: Ronald Pennings; Randall R Fields; Patrick Huygen; August F Deutman; William J Kimberling; Cor W R J Cremers
Usher syndrome type III can mimic other types of Usher syndrome.
The Annals of otology, rhinology, and laryngology 2003;112(6):525-30.
2003: Johannes M W van ven Ouweland; Kim Cryns; Ronald Pennings; Inge Walraven; George M C Janssen; J Antonie Maassen; Bernard F E Veldhuijzen; Alexander B Arntzenius; Dick Lindhout; Cor W R J Cremers; Guy Van Camp; Lambert D Dikkeschei
Molecular characterization of WFS1 in patients with Wolfram syndrome.
The Journal of molecular diagnostics : JMD 2003;5(2):88-95.
2003: Ronald Pennings; Steven J H Bom; Kim Cryns; Kris Flothmann; Patrick Huygen; Hannie Kremer; Guy Van Camp; Cor W R J Cremers
Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
Archives of otolaryngology--head & neck surgery 2003;129(4):421-6.
2003: Steven J H Bom; Martijn H Kemperman; Patrick Huygen; Mirjam W J Luijendijk; Cor W R J Cremers
Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH.
The Annals of otology, rhinology, and laryngology 2003;112(3):280-6.
2003: Els M R De Leenheer; Grétel G Oudesluijs; Anne Marie Kuijpers-Jagtman; Gudrun A Rappold; Rob C A Sengers; Cor W R J Cremers
Congenital conductive hearing loss in dyschondrosteosis.
The Annals of otology, rhinology, and laryngology 2003;112(2):153-8.
2003: Arjan de Brouwer; Ronald Pennings; Marjolijn Roeters; Peter Van Hauwe; Lisa M Astuto; Lies Hoefsloot; Patrick Huygen; Bellinda van den Helm; August F Deutman; Julie M Bork; William J Kimberling; Frans P M Cremers; Cor W R J Cremers; Hannie Kremer
Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family.
Human genetics 2003;112(2):156-63.
2003: Greet Vantrappen; Nathalie Rommel; Ann Swillen; Cor W R J Cremers; Jean-Pierre Fryns; koenraad devriendt
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.
Acta oto-rhino-laryngologica Belgica 2003;57(2):101-6.
2003: Arjan J Bosman; Myrthe K S Hol; Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Bone-anchored hearing aids in unilateral inner ear deafness.
Acta oto-laryngologica 2003;123(2):258-60.
2003: Ronald Pennings; Patrick Huygen; Michael D Weston; Annelies van Aarem; Michiel Wagenaar; William J Kimberling; Cor W R J Cremers
Pure tone hearing thresholds and speech recognition scores in Dutch patients carrying mutations in the USH2A gene.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(1):58-63.
2003: Niels van Heerbeek; Edith L G M Tonnaer; Koen J A O Ingels; Jo H A J Curfs; Cor W R J Cremers
Effect of exogenous surfactant on ventilatory and clearance function of the rat's eustachian tube.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(1):6-10.
2002: Ronald Pennings; Hannie Kremer; August F Deutman; William J Kimberling; Cor W R J Cremers
[From gene to disease; genetic causes of hearing loss and visual impairment sometimes accompanied by vestibular problems (Usher syndrome)].
Nederlands tijdschrift voor geneeskunde 2002;146(49):2354-8.
2002: Emmanuel A M Mylanus; Carina B Johansson; Cor W R J Cremers
Craniofacial titanium implants and chronic pain: histologic findings.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2002;23(6):920-5.
2002: Steven J H Bom; Guy Van Camp; Kim Cryns; Ronald J C Admiraal; Patrick Huygen; Cor W R J Cremers
Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2002;23(6):876-84.
2002: Martijn H Kemperman; Sacha M P Koch; Frank B M Joosten; Shrawan Kumar; Patrick Huygen; Cor W R J Cremers
Inner ear anomalies are frequent but nonobligatory features of the branchio-oto-renal syndrome.
Archives of otolaryngology--head & neck surgery 2002;128(9):1033-8.
2002: Cor W R J Cremers; J P De Mönnink; Neeltje J W Arts; Frank B M Joosten; Hannie Kremer; Lies Hoefsloot
Clinical report on the L95P mutation in a Dutch family with paraganglioma.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2002;23(5):755-9.
2002: Lisa M Astuto; Julie M Bork; Michael D Weston; James W Askew; R R Fields; Dana J Orten; S J Ohliger; Sheikh Amer Riazuddin; Robert J Morell; Shaheen Khan; S Riazuddin; Hannie Kremer; Peter Van Hauwe; CG Moller; Cor W R J Cremers; C Ayuso; John R Heckenlively; Klaus Rohrschneider; Ulrich H M Spandau; J Greenberg; Rajkumar Ramesar; William Reardon; P Bitoun; J Millan; R Legge; Thomas B Friedman; William J Kimberling
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
American journal of human genetics 2002;71(2):262-75.
2002: Els M R De Leenheer; Diederick van Zuijlen; Lut Van Laer; Guy Van Camp; Patrick Huygen; Egbert H Huizing; Cor W R J Cremers
Further delineation of the DFNA5 phenotype: results of speech recognition tests.
The Annals of otology, rhinology, and laryngology 2002;111(7 Pt 1):639-41.
2002: Guy Van Camp; Paul J Coucke; Jiro Akita; Erik Fransen; Satoko Abe; Els M R De Leenheer; Patrick Huygen; Cor W R J Cremers; Shin-ichi Usami
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.
Human mutation 2002;20(1):15-9.
2002: Ronald Pennings; Lambert D Dikkeschei; Cor W R J Cremers; Jody M W van den Ouweland
[From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)].
Nederlands tijdschrift voor geneeskunde 2002;146(21):985-7.
2002: Kim Cryns; Markus Pfister; Ronald Pennings; Steven J H Bom; Kris Flothmann; Goele Caethoven; Hannie Kremer; Isabelle Schatteman; Karen A Köln; Tímea Tóth; Susan Kupka; nikolaus blin; Peter Nürnberg; Holger Thiele; Paul H Van De Heyning; William Reardon; Dafydd Stephens; Cor W R J Cremers; Richard J H Smith; Guy Van Camp
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.
Human genetics 2002;110(5):389-94.
2002: Martijn H Kemperman; Lies Hoefsloot; Cor W R J Cremers
Hearing loss and connexin 26.
Journal of the Royal Society of Medicine 2002;95(4):171-7.
2002: Kris Van Den Bogaert; Paul J Govaerts; Els M R De Leenheer; Isabelle Schatteman; Margriet Verstreken; Wenjie Chen; Frank Declau; Cor W R J Cremers; Paul H Van De Heyning; F Erwin Offeciers; Thomas Somers; R J H Smith; Guy Van Camp
Otosclerosis: a genetically heterogeneous disease involving at least three different genes.
Bone 2002;30(4):624-30.
2002: Greet Vantrappen; Nathalie Rommel; Cor W R J Cremers; Jean-Pierre Fryns; koenraad devriendt
Mosaic trisomy 8 as a cause of velopharyngeal insufficiency.
American journal of medical genetics 2002;108(4):337-8.
2002: Theo A Peters; Edith L G M Tonnaer; Wim Kuijpers; Cor W R J Cremers; Jo H A J Curfs
Differences in endolymphatic sac mitochondria-rich cells indicate specific functions.
The Laryngoscope 2002;112(3):534-41.
2002: Els M R De Leenheer; Patrick Huygen; Paul J Coucke; Ronald J C Admiraal; Guy Van Camp; Cor W R J Cremers
Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 family.
The Annals of otology, rhinology, and laryngology 2002;111(3 Pt 1):267-74.
2002: S Ceruti; Christel Stinckens; Cor W R J Cremers; J W Casselman
Temporal bone anomalies in the branchio-oto-renal syndrome: detailed computed tomographic and magnetic resonance imaging findings.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2002;23(2):200-7.
2002: Lies Hoefsloot; Martijn H Kemperman; Cor W R J Cremers
[From gene to disease: deafness and connexin 26].
Nederlands tijdschrift voor geneeskunde 2002;146(6):259-61.
2002: Cor W R J Cremers
Surgery for acquired atresia of the external ear canal.
Clinical otolaryngology and allied sciences 2002;27(1):75-6.
2002: Martijn H Kemperman; Christel Stinckens; Shrawan Kumar; Frank B M Joosten; Patrick Huygen; Cor W R J Cremers
The branchio-oto-renal syndrome.
Advances in oto-rhino-laryngology 2002;61():192-200.
2002: Ronald Pennings; Michiel Wagenaar; Annelies van Aarem; Patrick Huygen; William J Kimberling; Cor W R J Cremers
Hearing impairment in Usher's syndrome.
Advances in oto-rhino-laryngology 2002;61():184-91.
2002: Robbert J H Ensink; Patrick Huygen; Cor W R J Cremers
The clinical spectrum of maternally transmitted hearing loss.
Advances in oto-rhino-laryngology 2002;61():172-83.
2002: Cor W R J Cremers; Ad F M Snik; Patrick Huygen; Frank B M Joosten; Frans P M Cremers
X-linked mixed deafness syndrome with congenital fixation of the stapedial footplate and perilymphatic gusher (DFN3).
Advances in oto-rhino-laryngology 2002;61():161-7.
2002: Christel Stinckens; Patrick Huygen; Guy Van Camp; Cor W R J Cremers
Pendred syndrome redefined. Report of a new family with fluctuating and progressive hearing loss.
Advances in oto-rhino-laryngology 2002;61():131-41.
2002: Patrick Huygen; Steven J H Bom; Guy Van Camp; Cor W R J Cremers
Clinical presentation of the DFNA loci where causative genes have not yet been cloned. DFNA4, DFNA6/14, DFNA7, DFNA16, DFNA20 and DFNA21.
Advances in oto-rhino-laryngology 2002;61():98-106.
2002: Els M R De Leenheer; Wyman T McGuirt; Henricus P M Kunst; Patrick Huygen; Richard J H Smith; Cor W R J Cremers
The phenotype of DFNA13/COL11A2.
Advances in oto-rhino-laryngology 2002;61():85-91.
2002: Els M R De Leenheer; Patrick Huygen; Sigrid Wayne; Margriet Verstreken; Frank Declau; Guy Van Camp; Paul H Van De Heyning; Richard J H Smith; Cor W R J Cremers
DFNA10/EYA4--the clinical picture.
Advances in oto-rhino-laryngology 2002;61():73-8.
2002: Martijn H Kemperman; Steven J H Bom; François X Lemaire; Wim I M Verhagen; Patrick Huygen; Cor W R J Cremers
DFNA9/COCH and its phenotype.
Advances in oto-rhino-laryngology 2002;61():66-72.
2002: Els M R De Leenheer; Diederick van Zuijlen; Lut Van Laer; Guy Van Camp; Patrick Huygen; Egbert H Huizing; Cor W R J Cremers
Clinical features of DFNA5.
Advances in oto-rhino-laryngology 2002;61():53-9.
2002: Els M R De Leenheer; Robbert J H Ensink; Henricus P M Kunst; Henri Marres; Zohreh Talebizadeh; Frank Declau; Shelley D Smith; Shin-ichi Usami; Paul H Van De Heyning; Guy Van Camp; Patrick Huygen; Cor W R J Cremers
DFNA2/KCNQ4 and its manifestations.
Advances in oto-rhino-laryngology 2002;61():41-6.
2002: Greet Vantrappen; Nathalie Rommel; W Wellens; Cor W R J Cremers; Jean-Pierre Fryns; koenraad devriendt
Autosomal dominant isolated velopharyngeal insufficiency.
Clinical genetics 2002;61(1):74-6.
2002: Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
The bone-anchored hearing aid in patients with a unilateral air-bone gap.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2002;23(1):61-6.
2001: Wim I M Verhagen; Steven J H Bom; Erik Fransen; Guy Van Camp; Patrick Huygen; E J Theunissen; Cor W R J Cremers
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family.
Clinical otolaryngology and allied sciences 2001;26(6):477-83.
2001: Ad F M Snik; Cor W R J Cremers
Vibrant semi-implantable hearing device with digital sound processing: effective gain and speech perception.
Archives of otolaryngology--head & neck surgery 2001;127(12):1433-7.
2001: Christel Stinckens; Patrick Huygen; Frank B M Joosten; Guy Van Camp; BJ Otten; Cor W R J Cremers
Fluctuant, progressive hearing loss associated with Menière like vertigo in three patients with the Pendred syndrome.
International journal of pediatric otorhinolaryngology 2001;61(3):207-15.
2001: Irina N Bespalova; Guy Van Camp; Steven J H Bom; David J Brown; Kim Cryns; A T DeWan; Ayse E Erson; Kris Flothmann; Henricus P M Kunst; P Kurnool; Theru A Sivakumaran; Cor W R J Cremers; S M Leal; Margit Burmeister; Marci M Lesperance
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.
Human molecular genetics 2001;10(22):2501-8.
2001: Martijn H Kemperman; Christel Stinckens; Shrawan Kumar; Patrick Huygen; Frank B M Joosten; Cor W R J Cremers
Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2001;22(5):637-43.
2001: Els M R De Leenheer; Patrick Huygen; Sigrid Wayne; Richard J H Smith; Cor W R J Cremers
The DFNA10 phenotype.
The Annals of otology, rhinology, and laryngology 2001;110(9):861-6.
2001: Steven J H Bom; Els M R De Leenheer; François X Lemaire; Martijn H Kemperman; Wim I M Verhagen; Henri Marres; Henricus P M Kunst; Robbert J H Ensink; Arjan J Bosman; Guy Van Camp; Frans P M Cremers; Patrick Huygen; Cor W R J Cremers
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH.
Archives of otolaryngology--head & neck surgery 2001;127(9):1045-8.
2001: Robbert J H Ensink; Patrick Huygen; Rikkert L Snoeckx; G Caethoven; Guy Van Camp; Cor W R J Cremers
A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13.
Clinical otolaryngology and allied sciences 2001;26(4):310-6.
2001: Christel Stinckens; L Standaert; J W Casselman; Patrick Huygen; Shrawan Kumar; J Van de Wallen; Cor W R J Cremers
The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family study.
International journal of pediatric otorhinolaryngology 2001;59(3):163-72.
2001: Arjan J Bosman; Ad F M Snik; Catharina T M van der Pouw; Emmanuel A M Mylanus; Cor W R J Cremers
Audiometric evaluation of bilaterally fitted bone-anchored hearing aids.
Audiology : official organ of the International Society of Audiology 2001;40(3):158-67.
2001: Andel G L van der Mey; Martijn J A Malessy; Johan H M Frijns; Edward Grooters; Cor W R J Cremers; K Graamans; André Grotenhuis; Jef J S Mulder
[Stereotaxic irradiation of vestibular schwannoma (acoustic neurinoma)].
Nederlands tijdschrift voor geneeskunde 2001;145(4):196-7.
2001: Theo A Peters; Edith L G M Tonnaer; Wim Kuijpers; Cor W R J Cremers; Jo H A J Curfs
Developmental aspects of the rat endolymphatic sac and functional implications.
Acta oto-laryngologica 2001;121(2):125-9.
2001: Erik Fransen; Margriet Verstreken; Steven J H Bom; François X Lemaire; Martijn H Kemperman; Yvette J M de Kok; Floris L Wuyts; Wim I M Verhagen; Patrick Huygen; Wyman T McGuirt; R J Smith; L V Van Maldergem; Frank Declau; Cor W R J Cremers; Paul H Van De Heyning; Frans P M Cremers; Guy Van Camp
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation.
Journal of medical genetics 2001;38(1):61-5.
2001: Greet Vantrappen; Nathalie Rommel; koenraad devriendt; Cor W R J Cremers; Louw Feenstra; Jean-Pierre Fryns
Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Acta oto-rhino-laryngologica Belgica 2001;55(1):43-8.
2001: Els M R De Leenheer; H H Kunst; Wyman T McGuirt; Sai D Prasad; MR Brown; Patrick Huygen; Richard J H Smith; Cor W R J Cremers
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).
Archives of otolaryngology--head & neck surgery 2001;127(1):13-7.
2000: Lisa M Astuto; Michael D Weston; C A Carney; Denise M Hoover; Cor W R J Cremers; Michiel Wagenaar; CG Moller; Richard J H Smith; S Pieke-Dahl; J Greenberg; Rajkumar Ramesar; SG Jacobson; C Ayuso; John R Heckenlively; M Tamayo; M B Gorin; William Reardon; William J Kimberling
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
American journal of human genetics 2000;67(6):1569-74.
2000: Michiel Wagenaar; H Schuknecht; J Nadol; M Benraad-Van Rens; S Pieke-Dahl; William J Kimberling; Cor W R J Cremers
Histopathologic features of the temporal bone in usher syndrome type I.
Archives of otolaryngology--head & neck surgery 2000;126(8):1018-23.
2000: Peter Van Hauwe; Paul J Coucke; Robbert J H Ensink; Patrick Huygen; Cor W R J Cremers; Guy Van Camp
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.
American journal of medical genetics 2000;93(3):184-7.
2000: Wim I M Verhagen; Steven J H Bom; Patrick Huygen; Erik Fransen; Guy Van Camp; Cor W R J Cremers
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9).
Archives of neurology 2000;57(7):1045-7.
2000: Sacha M P Koch; Shrawan Kumar; Cor W R J Cremers
A family with autosomal dominant inherited dysmorphic small auricles, lip pits, and congenital conductive hearing impairment.
Archives of otolaryngology--head & neck surgery 2000;126(5):639-44.
2000: S Kumar; K Deffenbacher; Henri Marres; Cor W R J Cremers; William J Kimberling
Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.
American journal of human genetics 2000;66(5):1715-20.
2000: S Pieke-Dahl; C G Möller; Philip M Kelley; Lisa M Astuto; Cor W R J Cremers; M B Gorin; William J Kimberling
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.
Journal of medical genetics 2000;37(4):256-62.
2000: Michael D Weston; James D Eudy; S Fujita; S Yao; Shin-ichi Usami; Cor W R J Cremers; J Greenberg; Rajkumar Ramesar; martini alessandro; CG Moller; Richard J H Smith; Janos Sumegi; William J Kimberling; J Greenburg
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.
American journal of human genetics 2000;66(4):1199-210.
2000: Henricus P M Kunst; C Huybrechts; Henri Marres; Patrick Huygen; Guy Van Camp; Cor W R J Cremers
The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.
The American journal of otology 2000;21(2):181-7.
2000: Ronald J C Admiraal; Han G Brunner; T L Dijkstra; Patrick Huygen; Cor W R J Cremers
Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.
The Laryngoscope 2000;110(3 Pt 1):457-61.
2000: Henricus P M Kunst; Henri Marres; Patrick Huygen; Gerard van Duijnhoven; A Krebsova; S van der Velde; A Reis; Frans P M Cremers; Cor W R J Cremers
Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21).
Clinical otolaryngology and allied sciences 2000;25(1):45-54.
2000: Frans P M Cremers; Cor W R J Cremers; Hans-Hilger Ropers
The ins and outs of X-linked deafness type 3.
Advances in oto-rhino-laryngology 2000;56():184-95.
2000: Cor W R J Cremers
Hearing: cracking the code.
The Journal of laryngology and otology 2000;114(1):6-16.
2000: Robbert J H Ensink; Patrick Huygen; Peter Van Hauwe; P Coucke; Cor W R J Cremers; Guy Van Camp
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2000;257(2):62-7.
2000: Dana J Orten; Michael D Weston; Philip M Kelley; Cor W R J Cremers; Michiel Wagenaar; SG Jacobson; William J Kimberling
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.
Human mutation 2000;15(1):114-5.
1999: Wyman T McGuirt; Sai D Prasad; Andrew J Griffith; Henricus P M Kunst; Glenn E Green; Karl B Shpargel; C Runge; C Huybrechts; Robert F Mueller; E Lynch; Mary-Claire King; H G Brunner; Cor W R J Cremers; M Takanosu; S W Li; M Arita; Richard Mayne; D J Prockop; Guy Van Camp; Richard J H Smith
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).
Nature genetics 1999;23(4):413-9.
1999: Michiel Wagenaar; P Draaijer; H Meek; H J ten Donkelaar; P Wesseling; William J Kimberling; Cor W R J Cremers
The cochlear nuclei in two patients with Usher syndrome type I.
International journal of pediatric otorhinolaryngology 1999;50(3):185-95.
1999: Ad F M Snik; Cor W R J Cremers
First audiometric results with the Vibrant soundbridge, a semi-implantable hearing device for sensorineural hearing loss.
Audiology : official organ of the International Society of Audiology 1999;38(6):335-8.
1999: Steven J H Bom; Henricus P M Kunst; Patrick Huygen; Frans P M Cremers; Cor W R J Cremers
Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.
British journal of audiology 1999;33(5):335-48.
1999: Frank Declau; Cor W R J Cremers; Paul Van de Heyning
Diagnosis and management strategies in congenital atresia of the external auditory canal. Study Group on Otological Malformations and Hearing Impairment.
British journal of audiology 1999;33(5):313-27.
1999: Dana J Orten; Michael D Weston; Philip M Kelley; Cor W R J Cremers; Michiel Wagenaar; SG Jacobson; William J Kimberling
Analysis of DNA elements that modulate myosin VIIA expression in humans.
Human mutation 1999;14(4):354.
1999: Steven J H Bom; Martijn H Kemperman; Yvette J M de Kok; Patrick Huygen; Wim I M Verhagen; Frans P M Cremers; Cor W R J Cremers
Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9.
The Laryngoscope 1999;109(9):1525-30.
1999: Guy Van Camp; Henricus P M Kunst; Kris Flothmann; Wyman T McGuirt; Jan Wauters; Henri Marres; Margriet Verstreken; Irina N Bespalova; Margit Burmeister; Paul H Van De Heyning; Richard J H Smith; Patrick J Willems; Cor W R J Cremers; Marci M Lesperance
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.
Journal of medical genetics 1999;36(7):532-6.
1999: Paul J Coucke; Peter Van Hauwe; P M Kelley; Henricus P M Kunst; Isabelle Schatteman; D Van Velzen; J Meyers; Robbert J H Ensink; Margriet Verstreken; Frank Declau; Henri Marres; K Kastury; S Bhasin; Wyman T McGuirt; Richard J H Smith; Cor W R J Cremers; Paul Van de Heyning; Patrick J Willems; Shelley D Smith; Guy Van Camp
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
Human molecular genetics 1999;8(7):1321-8.
1999: Catharina T M van der Pouw; Ad F M Snik; Cor W R J Cremers
The BAHA HC200/300 in comparison with conventional bone conduction hearing aids.
Clinical otolaryngology and allied sciences 1999;24(3):171-6.
1999: Catharina T M van der Pouw; Emmanuel A M Mylanus; Cor W R J Cremers
Percutaneous implants in the temporal bone for securing a bone conductor: surgical methods and results.
The Annals of otology, rhinology, and laryngology 1999;108(6):532-6.
1999: Henricus P M Kunst; Henri Marres; Patrick Huygen; Guy Van Camp; Frank B M Joosten; Cor W R J Cremers
Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.
Audiology : official organ of the International Society of Audiology 1999;38(3):165-73.
1999: Robbert J H Ensink; J P Sleeckx; Cor W R J Cremers
Proximal symphalangism and congenital conductive hearing loss: otologic aspects.
The American journal of otology 1999;20(3):344-9.
1999: Annelies van Aarem; Michiel Wagenaar; Edith L G M Tonnaer; S Pieke-Dahl; J Bisseling; H Janssen; B Bastiaans; William J Kimberling; Cor W R J Cremers
Semen analysis in the Usher syndrome type 2A.
ORL; journal for oto-rhino-laryngology and its related specialties 1999;61(3):126-30.
1999: Michiel Wagenaar; Annelies van Aarem; Patrick Huygen; S Pieke-Dahl; William J Kimberling; Cor W R J Cremers
Hearing impairment related to age in Usher syndrome types 1B and 2A.
Archives of otolaryngology--head & neck surgery 1999;125(4):441-5.
1999: Peter Van Hauwe; Paul J Coucke; Frank Declau; Henricus P M Kunst; Robbert J H Ensink; Henri Marres; Cor W R J Cremers; Bulantrisna Djelantik; Shelley D Smith; P Kelley; Paul H Van De Heyning; Guy Van Camp
Deafness linked to DFNA2: one locus but how many genes?
Nature genetics 1999;21(3):263.
1999: Yvette J M de Kok; Steven J H Bom; T M Brunt; Martijn H Kemperman; E van Beusekom; Saskia D van der Velde-Visser; Nahid G Robertson; Cynthia C Morton; Patrick Huygen; Wim I M Verhagen; Han G Brunner; Cor W R J Cremers; Frans P M Cremers
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.
Human molecular genetics 1999;8(2):361-6.
1999: Kristien Verhoeven; Robbert J H Ensink; V Tiranti; Patrick Huygen; DF Johnson; Isabelle Schatteman; Lut Van Laer; Margriet Verstreken; Paul Van de Heyning; Nathan Fischel-Ghodsian; M Zeviani; Cor W R J Cremers; Patrick J Willems; Guy Van Camp
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
European journal of human genetics : EJHG 1999;7(1):45-51.
1998: Greet Vantrappen; Nathalie Rommel; Cor W R J Cremers; koenraad devriendt; JP Frijns
The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.
International journal of pediatric otorhinolaryngology 1998;45(2):133-41.
1998: Cor W R J Cremers; Ronald J C Admiraal; Patrick Huygen; CH Bolder; LA Everett; Frank B M Joosten; Eric Green; Guy Van Camp; BJ Otten
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.
International journal of pediatric otorhinolaryngology 1998;45(2):113-23.
1998: Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Implantable hearing devices for sensorineural hearing loss: a review of the audiometric data.
Clinical otolaryngology and allied sciences 1998;23(5):414-9.
1998: Robbert J H Ensink; Kristien Verhoeven; Henri Marres; Patrick Huygen; G W Padberg; H ter Laak; Guy Van Camp; P J Willems; Cor W R J Cremers
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472.
Archives of otolaryngology--head & neck surgery 1998;124(8):886-91.
1998: Peter Van Hauwe; LA Everett; P Coucke; Daryl A Scott; M L Kraft; Carrie Ris Stalpers; CH Bolder; BJ Otten; Jan J M de Vijlder; N L Dietrich; Arabandi Ramesh; S C Srisailapathy; A Parving; Cor W R J Cremers; Patrick J Willems; Richard J H Smith; Eric Green; Guy Van Camp
Two frequent missense mutations in Pendred syndrome.
Human molecular genetics 1998;7(7):1099-104.
1998: James D Eudy; Michael D Weston; S Yao; Denise M Hoover; Heidi L Rehm; M Ma-Edmonds; Denise Yan; Iqbal Ahmad; J J Cheng; C Ayuso; Cor W R J Cremers; S Davenport; CG Moller; Catherine B Talmadge; Kirk W Beisel; M Tamayo; Cynthia C Morton; Anand Swaroop; William J Kimberling; Janos Sumegi
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Science (New York, N.Y.) 1998;280(5370):1753-7.
1998: S Kumar; Henri Marres; Cor W R J Cremers; William J Kimberling
Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13.
American journal of medical genetics 1998;76(5):395-401.
1998: K T van der Pouw; Ad F M Snik; Cor W R J Cremers
Audiometric results of bilateral bone-anchored hearing aid application in patients with bilateral congenital aural atresia.
The Laryngoscope 1998;108(4 Pt 1):548-53.
1998: Emmanuel A M Mylanus; K C van der Pouw; Ad F M Snik; Cor W R J Cremers
Intraindividual comparison of the bone-anchored hearing aid and air-conduction hearing aids.
Archives of otolaryngology--head & neck surgery 1998;124(3):271-6.
1998: Ad F M Snik; Andy J Beynon; Emmanuel A M Mylanus; Catharina T M van der Pouw; Cor W R J Cremers
Binaural application of the bone-anchored hearing aid.
The Annals of otology, rhinology, and laryngology 1998;107(3):187-93.
1998: Annelies van Aarem; H L Muytjens; M M Smits; Cor W R J Cremers
Recurrent therapy resistant mastoiditis by Mycobacterium cheilonae abscessus, a nontuberculous mycobacterium.
International journal of pediatric otorhinolaryngology 1998;43(1):61-72.
1998: Henricus P M Kunst; Henri Marres; Guy Van Camp; Cor W R J Cremers
Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research.
Clinical otolaryngology and allied sciences 1998;23(1):9-17.
1998: Robbert J H Ensink; G V Camp; Cor W R J Cremers
Mitochondrial inherited hearing loss.
Clinical otolaryngology and allied sciences 1998;23(1):3-8.
1998: Catharina T M van der Pouw; P Carlsson; Cor W R J Cremers; Ad F M Snik
A new more powerful bone-anchored hearing aid: first results.
Scandinavian audiology 1998;27(3):179-82.
1998: S Kumar; William J Kimberling; Michael D Weston; B G Schaefer; M A Berg; Henri Marres; Cor W R J Cremers
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome.
Human mutation 1998;11(6):443-9.
1998: Catharina T M van der Pouw; Carina B Johansson; Emmanuel A M Mylanus; T Albrektsson; Cor W R J Cremers
Removal of titanium implants from the temporal bone: histologic findings.
The American journal of otology 1998;19(1):46-51.
1998: Frans A Hol; MP Geurds; Cor W R J Cremers; Ben C J Hamel; Edwin C M Mariman
Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X).
Human mutation 1998;Suppl 1():S145-7.
1998: Henricus P M Kunst; Henri Marres; Patrick Huygen; Robbert J H Ensink; Guy Van Camp; Peter Van Hauwe; P Coucke; P Willems; Cor W R J Cremers
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2.
The Laryngoscope 1998;108(1 Pt 1):74-80.
1997: Henri Marres; M van Ewijk; Patrick Huygen; Henricus P M Kunst; Guy Van Camp; P Coucke; P Willems; Cor W R J Cremers
Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2.
Archives of otolaryngology--head & neck surgery 1997;123(6):573-7.
1997: Guy Van Camp; Paul J Coucke; Henricus P M Kunst; Isabelle Schatteman; D Van Velzen; Henri Marres; M van Ewijk; Frank Declau; Peter Van Hauwe; J Meyers; J Kenyon; Shelley D Smith; Richard J H Smith; Bulantrisna Djelantik; Cor W R J Cremers; Paul H Van De Heyning; Patrick J Willems
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p.
Genomics 1997;41(1):70-4.
1997: P Coucke; Guy Van Camp; O Demirhan; Y Kabakkaya; Wendy Balemans; Peter Van Hauwe; T Van Agtmael; Richard J H Smith; A Parving; CH Bolder; Cor W R J Cremers; Patrick J Willems
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q.
Genomics 1997;40(1):48-54.
1997: P M Struycken; Cor W R J Cremers; E C Mariman; Frank B M Joosten; R J Bleker
Glomus tumours and genomic imprinting: influence of inheritance along the paternal or maternal line.
Clinical otolaryngology and allied sciences 1997;22(1):71-6.
1997: Christel Stinckens; Robbert J H Ensink; L Feenstra; Jean-Pierre Fryns; Cor W R J Cremers
Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes.
International journal of pediatric otorhinolaryngology 1997;38(3):237-45.
1997: S Kumar; K Deffenbacher; Cor W R J Cremers; G Van Camp; William J Kimberling
Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing.
Genetic testing 1997;1(4):243-51.
1997: Robbert J H Ensink; Han G Brunner; Cor W R J Cremers
A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive trait.
Genetic counseling (Geneva, Switzerland) 1997;8(4):285-90.
1997: Yvette J M de Kok; Cor W R J Cremers; Hans-Hilger Ropers; Frans P M Cremers
The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation.
Human mutation 1997;10(3):207-11.
1997: Robbert J H Ensink; Cor W R J Cremers; Han G Brunner
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome.
Archives of otolaryngology--head & neck surgery 1997;123(1):97-9.
1996: Annelies van Aarem; Alfred J L G Pinckers; William J Kimberling; Patrick Huygen; EM Bleeker-Wagemakers; Cor W R J Cremers
Stable and progressive hearing loss in type 2A Usher's syndrome.
The Annals of otology, rhinology, and laryngology 1996;105(12):962-7.
1996: Michiel Wagenaar; Ad F M Snik; William J Kimberling; Cor W R J Cremers
Carriers of the Usher syndrome type IB: is audiometric identification possible?
The American journal of otology 1996;17(6):853-8.
1996: Michael D Weston; Philip M Kelley; L D Overbeck; Michiel Wagenaar; Dana J Orten; Tama Hasson; Z Y Chen; David P Corey; Mark S Mooseker; Janos Sumegi; Cor W R J Cremers; C Moller; S G Jacobson; M B Gorin; William J Kimberling
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
American journal of human genetics 1996;59(5):1074-83.
1996: Robbert J H Ensink; Henri Marres; Han G Brunner; Cor W R J Cremers
Hearing loss in the Saethre-Chotzen syndrome.
The Journal of laryngology and otology 1996;110(10):952-7.
1996: Patrick Huygen; Cor W R J Cremers; Wim I M Verhagen; Frank B M Joosten
Camurati-Engelmann disease presenting as 'juvenile otosclerosis'.
International journal of pediatric otorhinolaryngology 1996;37(2):129-41.
1996: S Pieke-Dahl; Annelies van Aarem; A Dobin; Cor W R J Cremers; William J Kimberling
Genetic heterogeneity of Usher syndrome type II in a Dutch population.
Journal of medical genetics 1996;33(9):753-7.
1996: Yvette J M de Kok; E R Vossenaar; Cor W R J Cremers; Niklas Dahl; Jocelyn Laporte; L J Hu; Didier Lacombe; Nathan Fischel-Ghodsian; R A Friedman; L S Parnes; P Thorpe; Maria Bitner-Glindzicz; H J Pander; H Heilbronner; J Graveline; J T den Dunnen; Han G Brunner; Hans-Hilger Ropers; Frans P M Cremers
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4.
Human molecular genetics 1996;5(9):1229-35.
1996: J P van Leeuwen; J C Braspenning; H Meijer; Cor W R J Cremers
Quality of life after acoustic neuroma surgery.
The Annals of otology, rhinology, and laryngology 1996;105(6):423-30.
1996: J P van Leeuwen; B S Harhangi; N P Thewissen; H O Thijssen; Cor W R J Cremers
Delays in the diagnosis of acoustic neuromas.
The American journal of otology 1996;17(2):321-5.
1996: S Kumar; William J Kimberling; Arpad Lanyi; Janos Sumegi; J Pinnt; P Ing; S Tinley; H A Marres; Cor W R J Cremers
Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.
Genomics 1996;31(1):71-9.
1995: Annelies van Aarem; Michiel Wagenaar; Alfred J L G Pinckers; Patrick Huygen; EM Bleeker-Wagemakers; B J Kimberling; Cor W R J Cremers
Ophthalmologic findings in Usher syndrome type 2A.
Ophthalmic genetics 1995;16(4):151-8.
1995: J P van Leeuwen; M Pruszczynski; Henri Marres; André Grotenhuis; Cor W R J Cremers
Unilateral hearing loss due to a rhabdomyoma in a six-year-old child.
The Journal of laryngology and otology 1995;109(12):1186-9.
1995: Michiel Wagenaar; B ter Rahe; Annelies van Aarem; Patrick Huygen; Ronald J C Admiraal; EM Bleeker-Wagemakers; A Pinckers; William J Kimberling; Cor W R J Cremers
Clinical findings in obligate carriers of type I Usher syndrome.
American journal of medical genetics 1995;59(3):375-9.
1995: P B van Vierzen; Frank B M Joosten; Henri Marres; Cor W R J Cremers; J H Ruijs
Mandibulofacial dysostosis: CT findings of the temporal bones.
European journal of radiology 1995;21(1):53-7.
1995: A Chen; M Francis; L Ni; Cor W R J Cremers; W J Kimberling; Y Sato; PD Phelps; S C Bellman; M J Wagner; Marcus E Pembrey
Phenotypic manifestations of branchio-oto-renal syndrome.
American journal of medical genetics 1995;58(4):365-70.
1995: J P van Leeuwen; Cor W R J Cremers; N P Thewissen; B S Harhangi; E Meijer
Acoustic neuroma: correlation among tumor size, symptoms, and patient age.
The Laryngoscope 1995;105(7 Pt 1):701-7.
1995: Cor W R J Cremers; E H Strübbe; W N Willemsen
Stapedial ankylosis in the Mayer-Rokitansky-Küster-Hauser syndrome.
Archives of otolaryngology--head & neck surgery 1995;121(7):800-3.
1995: Cor W R J Cremers; S D Brown; K P Steel; H G Brunner; A P Read; William J Kimberling
Gene linkage and genetic deafness.
International journal of pediatric otorhinolaryngology 1995;32 Suppl():S167-74.
1995: Henri Marres; Cor W R J Cremers; Michael J Dixon; Patrick Huygen; Frank B M Joosten
The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees.
Archives of otolaryngology--head & neck surgery 1995;121(5):509-14.
1995: Emmanuel A M Mylanus; Ad F M Snik; Cor W R J Cremers
Patients' opinions of bone-anchored vs conventional hearing aids.
Archives of otolaryngology--head & neck surgery 1995;121(4):421-5.
1995: Ad F M Snik; G C Hombergen; Emmanuel A M Mylanus; Cor W R J Cremers
Air-bone gap in patients with X-linked stapes gusher syndrome.
The American journal of otology 1995;16(2):241-6.
1995: Annelies van Aarem; Cor W R J Cremers; Alfred J L G Pinckers; Patrick Huygen; G C Hombergen; B J Kimberling
The Usher syndrome type 2A: clinical findings in obligate carriers.
International journal of pediatric otorhinolaryngology 1995;31(2-3):159-74.
1995: Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Bone-anchored hearing aids in patients with sensorineural hearing loss and persistent otitis externa.
Clinical otolaryngology and allied sciences 1995;20(1):31-5.
1995: Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
The bone-anchored hearing aid compared with conventional hearing aids. Audiologic results and the patients' opinions.
Otolaryngologic clinics of North America 1995;28(1):73-83.
1995: Henri Marres; Cor W R J Cremers; E H Marres; Patrick Huygen
Ear surgery in Treacher Collins syndrome.
The Annals of otology, rhinology, and laryngology 1995;104(1):31-41.
1995: William J Kimberling; Michael D Weston; C Möller; A van Aarem; Cor W R J Cremers; Janos Sumegi; P S Ing; C Connolly; martini alessandro; M Milani
Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.
American journal of human genetics 1995;56(1):216-23.
1995: Edwin C M Mariman; Sylvia van Beersum; Cor W R J Cremers; P M Struycken; Hans-Hilger Ropers
Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity.
Human genetics 1995;95(1):56-62.
1994: S Kumar; William J Kimberling; C J Connolly; S Tinley; H A Marres; Cor W R J Cremers
Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.
American journal of human genetics 1994;55(6):1188-94.
1994: J P Van Leeuwen; Cor W R J Cremers; E J Theunissen; E H Marres; E Meyer
Translabyrinthine and transotic surgery for acoustic neuroma.
Clinical otolaryngology and allied sciences 1994;19(6):491-5.
1994: Emmanuel A M Mylanus; Cor W R J Cremers
A one-stage surgical procedure for placement of percutaneous implants for the bone-anchored hearing aid.
The Journal of laryngology and otology 1994;108(12):1031-5.
1994: P Coucke; Guy Van Camp; B Djoyodiharjo; Shelley D Smith; R R Frants; G W Padberg; J K Darby; Egbert H Huizing; Cor W R J Cremers; W J Kimberling
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.
The New England journal of medicine 1994;331(7):425-31.
1994: Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Aided free-field thresholds in children with conductive hearing loss fitted with air- or bone-conduction hearing aids.
International journal of pediatric otorhinolaryngology 1994;30(2):133-42.
1994: Cor W R J Cremers; P M van Rijn; Patrick Huygen
The sex-ratio in childhood deafness, an analysis of the male predominance.
International journal of pediatric otorhinolaryngology 1994;30(2):105-10.
1994: Emmanuel A M Mylanus; Andy J Beynon; Ad F M Snik; Cor W R J Cremers
Percutaneous titanium implantation in the skull for the bone-anchored hearing aid.
Journal of investigative surgery : the official journal of the Academy of Surgical Research 1994;7(4):327-32.
1994: E H Strübbe; Cor W R J Cremers; F G Dikkers; W N Willemsen
Hearing loss and the Mayer-Rokitansky-Küster-Hauser syndrome.
The American journal of otology 1994;15(3):431-6.
1994: Emmanuel A M Mylanus; F M Snik; Cor W R J Cremers; F F Jorritsma; H Verschuure
Audiological results of the bone-anchored hearing aid HC200: multicenter results.
The Annals of otology, rhinology, and laryngology 1994;103(5 Pt 1):368-74.
1994: Emmanuel A M Mylanus; Ad F M Snik; F F Jorritsma; Cor W R J Cremers
Audiologic results for the bone-anchored hearing aid HC220.
Ear and hearing 1994;15(1):87-92.
1994: Ad F M Snik; Emmanuel A M Mylanus; Cor W R J Cremers
Speech recognition with the bone-anchored hearing aid determined objectively and subjectively.
Ear, nose, & throat journal 1994;73(2):115-7.
1994: H von Bokhoven; C von Genderen; C M Molloy; Dorien J R van De Pol; Cor W R J Cremers; A von Aarem; Marianne Schwartz; T Rosenberg; A H Geurts van Kessel; Hans-Hilger Ropers
Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type II.
Genomics 1994;19(2):385-7.
1994: Emmanuel A M Mylanus; Cor W R J Cremers; Ad F M Snik; N W van den Berge
Clinical results of percutaneous implants in the temporal bone.
Archives of otolaryngology--head & neck surgery 1994;120(1):81-5.
1994: Henri Marres; Cor W R J Cremers; Patrick Huygen; Frank B M Joosten
The deafness, pre-auricular sinus, external ear anomaly and commissural lip pits syndrome--otological, vestibular and radiological findings.
The Journal of laryngology and otology 1994;108(1):13-8.
1994: Emmanuel A M Mylanus; Ad F M Snik; Cor W R J Cremers
Influence of the thickness of the skin and subcutaneous tissue covering the mastoid on bone-conduction thresholds obtained transcutaneously versus percutaneously.
Scandinavian audiology 1994;23(3):201-3.
1993: Cor W R J Cremers; Henri Marres; H G Brunner
Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndrome.
The Laryngoscope 1993;103(10):1186-9.
1993: Edwin C M Mariman; Sylvia van Beersum; Cor W R J Cremers; F M van Baars; Hans-Hilger Ropers
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q.
Human genetics 1993;91(4):357-61.
1993: J P van Leeuwen; Cor W R J Cremers; H O Thijssen; H E Meyer
Unchanged unilateral hearing loss and ipsilateral growth of an acoustic neuroma from 1 to 4 cm.
The Journal of laryngology and otology 1993;107(3):230-2.
1993: Patrick Huygen; P M van Rijn; Cor W R J Cremers; E J Theunissen
The vestibulo-ocular reflex in pupils at a Dutch school for the hearing impaired; findings relating to acquired causes.
International journal of pediatric otorhinolaryngology 1993;25(1-3):39-47.
1993: E Teunissen; Cor W R J Cremers
Surgery for congenital anomalies of the middle ear with mobile stapes.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 1993;250(6):327-31.
1992: S Kumar; William J Kimberling; J B Kenyon; R J Smith; H A Marres; Cor W R J Cremers
Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.
Human molecular genetics 1992;1(7):491-5.
1992: I Bach; Han G Brunner; P Beighton; R H Ruvalcaba; W Reardon; Marcus E Pembrey; Saskia D van der Velde-Visser; G A Bruns; Cor W R J Cremers; Frans P M Cremers
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3).
American journal of human genetics 1992;51(1):38-44.
1992: Cor W R J Cremers; F M Snik; Andy J Beynon
Hearing with the bone-anchored hearing aid (BAHA, HC 200) compared to a conventional bone-conduction hearing aid.
Clinical otolaryngology and allied sciences 1992;17(3):275-9.
1992: Cor W R J Cremers; C J van der Burgt
Hearing loss in Noonan syndrome.
International journal of pediatric otorhinolaryngology 1992;23(1):81-4.
1992: Ad F M Snik; F F Jorritsma; Cor W R J Cremers; Andy J Beynon; N W van den Berge
The super-bass bone-anchored hearing aid compared to conventional hearing aids. Audiological results and the patients' opinions.
Scandinavian audiology 1992;21(3):157-61.
1991: Cor W R J Cremers; J M Beusen; Patrick Huygen
Hearing gain after stapedotomy, partial platinectomy, or total stapedectomy for otosclerosis.
The Annals of otology, rhinology, and laryngology 1991;100(12):959-61.
1991: Henri Marres; Cor W R J Cremers
Congenital conductive or mixed deafness, preauricular sinus, external ear anomaly, and commissural lip pits: an autosomal dominant inherited syndrome.
The Annals of otology, rhinology, and laryngology 1991;100(11):928-32.
1991: Cor W R J Cremers; E Teunissen
The impact of a syndromal diagnosis on surgery for congenital minor ear anomalies.
International journal of pediatric otorhinolaryngology 1991;22(1):59-74.
1991: B Teunissen; Cor W R J Cremers
Surgery for congenital stapes ankylosis with an associated congenital ossicular chain anomaly.
International journal of pediatric otorhinolaryngology 1991;21(3):217-26.
1991: Cor W R J Cremers; Ad F M Snik; Andy J Beynon
[A hearing aid anchored in the cranial bone for amplification of bone conduction].
Nederlands tijdschrift voor geneeskunde 1991;135(11):468-71.
1991: T J Garretsen; Cor W R J Cremers
Stapes surgery in osteogenesis imperfecta: analysis of postoperative hearing loss.
The Annals of otology, rhinology, and laryngology 1991;100(2):120-30.
1991: K Comeau; William J Kimberling; Cor W R J Cremers; Yin Yao Shugart
The search for branchiootorenal syndrome on chromosomes 1 and 8.
Annals of the New York Academy of Sciences 1991;630():288-9.
1991: T J Garretsen; Cor W R J Cremers
Clinical and genetic aspects in autosomal dominant inherited osteogenesis imperfecta type I.
Annals of the New York Academy of Sciences 1991;630():240-8.
1991: Cor W R J Cremers; P M van Rijn
Acquired causes of deafness in childhood.
Annals of the New York Academy of Sciences 1991;630():197-202.
1991: Cor W R J Cremers; Henri Marres; P M van Rijn
Nonsyndromal profound genetic deafness in childhood.
Annals of the New York Academy of Sciences 1991;630():191-6.
1991: Han G Brunner; B Smeets; D Smeets; M Nelen; Cor W R J Cremers; Hans-Hilger Ropers
Molecular genetics of X-linked hearing impairment.
Annals of the New York Academy of Sciences 1991;630():176-90.
1990: T J Garretsen; Cor W R J Cremers
Ear surgery in osteogenesis imperfecta. Clinical findings and short-term and long-term results.
Archives of otolaryngology--head & neck surgery 1990;116(3):317-23.
1989: Cor W R J Cremers; T Garretsen
Stapes surgery in osteogenesis imperfecta.
The American journal of otology 1989;10(6):474-6.
1989: Henri Marres; Cor W R J Cremers; Piet Hein Jongbloet
Hearing levels in the Cornelia de Lange syndrome. A report of seven cases.
International journal of pediatric otorhinolaryngology 1989;18(1):31-7.
1989: Cor W R J Cremers; P M van Rijn; M J Hageman
Prevention of serious hearing impairment of deafness in the young child.
Journal of the Royal Society of Medicine 1989;82(8):484-7.
1989: Henri Marres; Cor W R J Cremers
Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers.
Archives of otolaryngology--head & neck surgery 1989;115(5):591-5.
1988: Cor W R J Cremers; W J Delleman
Usher's syndrome, temporal bone pathology.
International journal of pediatric otorhinolaryngology 1988;16(1):23-30.
1988: P M van Rijn; Cor W R J Cremers
Surgery for congenital conductive deafness in Klippel-Feil syndrome.
The Annals of otology, rhinology, and laryngology 1988;97(4 Pt 1):347-52.
1988: Cor W R J Cremers; E Teunissen; E H Marres
Classification of congenital aural atresia and results of reconstructive surgery.
Advances in oto-rhino-laryngology 1988;40():9-14.
1987: Cor W R J Cremers; P van Rijn; B ter Haar
Autosomal recessive progressive high-frequency sensorineural deafness in childhood.
Archives of otolaryngology--head & neck surgery 1987;113(12):1319-24.
1987: Cor W R J Cremers; M J Hageman; P M van Rijn
[Prevention of severe hard-of-hearing or deafness in young children].
Nederlands tijdschrift voor geneeskunde 1987;131(17):703-6.
1987: Cor W R J Cremers; E H Marres
An additional classification for congenital aural atresia. Its impact on the predictability of surgical results.
Acta oto-rhino-laryngologica Belgica 1987;41(4):596-601.
1985: Cor W R J Cremers; G C Hombergen; J J Scaf; Patrick Huygen; W S Volkers; Alfred J L G Pinckers
X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery.
Archives of otolaryngology (Chicago, Ill. : 1960) 1985;111(4):249-54.