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Cor Cremers

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

Concepts & Ideas

Procedures

Devices

Hearing Aids

Physiology

Genes & Molecular Sequences

Dominant Genes

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Netherlands

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Publications

TOP 3
Verhaegen Veronique J O; Mulder Jef J S; Mylanus Emmanuel A M; Cremers Cor W R J; Snik Ad F M
Profound mixed hearing loss: bone-anchored hearing aid system or cochlear implant?
de Wolf Maarten J F; Leijendeckers Joop M; Mylanus Emmanuel A M; Hol Myrthe K S; Snik Ad F M; Cremers Cor W R J
Age-related use and benefit of the bone-anchored hearing aid compact.
Pennings Ronald J E; Liauw Lishya; Cremers Cor W R J
A spontaneous otogenic extradural pneumocephalus.

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All Publications

2009: Verhaegen Veronique J O; Mulder Jef J S; Mylanus Emmanuel A M; Cremers Cor W R J; Snik Ad F M
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: de Wolf Maarten J F; Leijendeckers Joop M; Mylanus Emmanuel A M; Hol Myrthe K S; Snik Ad F M; Cremers Cor W R J
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: Pennings Ronald J E; Liauw Lishya; Cremers Cor W R J
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: Faber Hubert T; de Wolf Maarten J F; de Rooy Jacky W J; Hol Myrthe K S; Cremers Cor W R J; Mylanus Emmanuel A M
Bone-anchored hearing aid implant location in relation to skin reactions.
Archives of otolaryngology--head & neck surgery 2009;135(8):742-7.
2009: Hao Huai-Xiang; Khalimonchuk Oleh; Schraders Margit; Dephoure Noah; Bayley Jean-Pierre; Kunst Henricus; Devilee Peter; Cremers Cor W R J; Schiffman Joshua D; Bentz Brandon G; Gygi Steven P; Winge Dennis R; Kremer Hannie; Rutter Jared
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.
Science (New York, N.Y.) 2009;325(5944):1139-42.
2009: de Wolf Maarten J F; Hol Myrthe K S; Mylanus Emmanuel A M; Cremers Cor W R J
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: Timmer Ferdinand C A; Hanssens Patrick E J; van Haren Anniek E P; Mulder Jef J S; Cremers Cor W R J; Beynon Andy J; van Overbeeke Jacobus J; Graamans Kees
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: Swinnen Freya K R; De Leenheer Els M R; Coucke Paul J; Cremers Cor W R J; Dhooge Ingeborg J M
Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta.
The Laryngoscope 2009;119(6):1171-9.
2009: de Heer Anne-Martine R; Huygen Patrick L M; Collin Rob W J; Oostrik Jaap; Kremer Hannie; Cremers Cor W R J
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: van der Avoort Stijn J C; van Heerbeek Niels; Zielhuis Gerhard A; Cremers Cor W R J
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: Artz Janneke C J M; Timmer Ferdinand C A; Mulder Jef J S; Cremers Cor W R J; Graamans Kees
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: de Heer Anne-Martine R; Huygen Patrick L M; Collin Rob W J; Kremer Hannie; Cremers Cor W R J
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: Pennings Ronald J E; Cremers Cor W R J
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: Schrauwen Isabelle; Ealy Megan; Huentelman Matthew J; Thys Melissa; Homer Nils; Vanderstraeten Kathleen; Fransen Erik; Corneveaux Jason J; Craig David W; Claustres Mireille; Cremers Cor W R J; Dhooge Ingeborg; Van de Heyning Paul; Vincent Robert; Offeciers Erwin; Smith Richard J H; Van Camp Guy
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: van Drunen F J Wendy; Pauw Robert J; Collin Rob W J; Kremer Hannie; Huygen Patrick L M; Cremers Cor W R J
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3.
Audiology & neuro-otology 2009;14(5):303-7.
2009: Leijendeckers Joop M; Pennings Ronald J E; Snik Ad F M; Bosman Arjan J; Cremers Cor W R J
Audiometric characteristics of USH2a patients.
Audiology & neuro-otology 2009;14(4):223-31.
2008: de Wolf Maarten J F; Hol Myrthe K S; Huygen Patrick L M; Mylanus Emmanuel A M; Cremers Cor W R J
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: Collin Rob W J; de Heer Anne-Martine R; Oostrik Jaap; Pauw Robert-Jan; Plantinga Rutger F; Huygen Patrick L; Admiraal Ronald; de Brouwer Arjan P M; Strom Tim M; Cremers Cor W R J; Kremer Hannie
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: Verhagen C V M; Hol M K S; Coppens-Schellekens W; Snik A F M; Cremers C W R J
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: Snik Ad; Leijendeckers Joop; Hol Myrthe; Mylanus Emmanuel; Cremers Cor
The bone-anchored hearing aid for children: recent developments.
International journal of audiology 2008;47(9):554-9.
2008: Verhaegen Veronique J O; Mylanus Emmanuel A M; Cremers Cor W R J; Snik Ad F M
Audiological application criteria for implantable hearing aid devices: a clinical experience at the Nijmegen ORL clinic.
The Laryngoscope 2008;118(9):1645-9.
2008: Plantinga Rutger F; Pennings Ronald J E; Huygen Patrick L M; Bruno Rocco; Eller Philipp; Barrett Timothy G; Vialettes Bernard; Paquis-Fluklinger Veronique; Lombardo Fortunato; Cremers Cor W R J
Hearing impairment in genotyped Wolfram syndrome patients.
The Annals of otology, rhinology, and laryngology 2008;117(7):494-500.
2008: van der Avoort Stijn J C; van Heerbeek Niels; Admiraal Ronald J C; Zielhuis Gerhard A; Cremers Cor W R J
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: Kunst Sylvia J W; Hol Myrthe K S; Mylanus Emmanuel A M; Leijendeckers Joop M; Snik Ad F M; Cremers Cor W R J
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: Kochhar Amit; Orten Dana J; Sorensen Jessica L; Fischer Stephanie M; Cremers Cor W R J; Kimberling William J; Smith Richard J H
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
Human mutation 2008;29(4):565.
2008: Collin Rob W J; Chellappa Ramesh; Pauw Robert-Jan; Vriend Gert; Oostrik Jaap; van Drunen Wendy; Huygen Patrick L; Admiraal Ronald; Hoefsloot Lies H; Cremers Frans P M; Xiang Mengqing; Cremers Cor W R J; Kremer Hannie
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: Orten Dana J; Fischer Stephanie M; Sorensen Jessica L; Radhakrishna Uppala; Cremers Cor W R J; Marres Henri A M; Van Camp Guy; Welch Katherine O; Smith Richard J H; Kimberling William J
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: Pauw Robert J; van Drunen F J Wendy; Collin Rob W J; Huygen Patrick L M; Kremer Hannie; Cremers Cor W R J
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: Kunst Sylvia J W; Leijendeckers Joop M; Mylanus Emmanuel A M; Hol Myrthe K S; Snik Ad F M; Cremers Cor W R J
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: Collin Rob W J; Kalay Ersan; Tariq Muhammad; Peters Theo; van der Zwaag Bert; Venselaar Hanka; Oostrik Jaap; Lee Kwanghyuk; Ahmed Zubair M; Caylan Refik; Li Yun; Spierenburg Henk A; Eyupoglu Erol; Heister Angelien; Riazuddin Saima; Bahat Elif; Ansar Muhammad; Arslan Selcuk; Wollnik Bernd; Brunner Han G; Cremers Cor W R J; Karaguzel Ahmet; Ahmad Wasim; Cremers Frans P M; Vriend Gert; Friedman Thomas B; Riazuddin Sheikh; Leal Suzanne M; Kremer Hannie
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: Cremers C W R J
[Turner syndrome in adulthood]
Nederlands tijdschrift voor geneeskunde 2007;151(42):2353-4; author reply 2354.
2007: Kalay Ersan; Uzumcu Abdullah; Krieger Elmar; Caylan Refik; Uyguner Oya; Ulubil-Emiroglu Melike; Erdol Hidayet; Kayserili Hülya; Hafiz Gunter; Baserer Nermin; Heister Angelien J G M; Hennies Hans C; Nürnberg Peter; Basaran Seher; Brunner Han G; Cremers Cor W R J; Karaguzel Ahmet; Wollnik Bernd; Kremer Hannie
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: Kunst Sylvia J W; Hol Myrthe K; Cremers Cor W; Mylanus Emmanuel A
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: van Heerbeek Niels; van der Avoort Stijn J C; Zielhuis Gerhard A; Cremers Cor W R J
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: Pauw Robert Jan; Huygen Patrick L M; Thys Melissa; Van Camp Guy; Joosten Frank B M; Cremers Cor W R J
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: Collin Rob W J; Kalay Ersan; Oostrik Jaap; Caylan Refik; Wollnik Bernd; Arslan Selçuk; den Hollander Anneke I; Birinci Yelda; Lichtner Peter; Strom Tim M; Toraman Bayram; Hoefsloot Lies H; Cremers Cor W R J; Brunner Han G; Cremers Frans P M; Karaguzel Ahmet; Kremer Hannie
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.
Human mutation 2007;28(7):718-23.
2007: Snik Ad F M; van Duijnhoven Noortje T L; Mulder Jef J S; Cremers Cor W R J
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: Pauw Robert J; Huygen Patrick L M; Collin Rob W J; Cruysberg Johannes R M; Hoefsloot Lies H; Kremer Hannie; Cremers Cor W R J
Phenotype description of a novel DFNA9/COCH mutation, I109T.
The Annals of otology, rhinology, and laryngology 2007;116(5):349-57.
2007: Bischoff Anne M L C; Pauw Robert J; Huygen Patrick L M; Aandekerk Albert L; Kremer Hannie; Cremers Cor W R J; Cruysberg Johannes R M
Vertical corneal striae in families with autosomal dominant hearing loss: DFNA9/COCH.
American journal of ophthalmology 2007;143(5):847-852.
2007: Kalay E; Caylan R; Kiroglu A F; Yasar T; Collin R W J; Heister J G A M; Oostrik J; Cremers C W R J; Brunner H G; Karaguzel A; Kremer H
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: Cremers C W R J; Plantinga R F; Kremer H
[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: Plantinga Rutger F; Cremers Cor W R J; Huygen Patrick L M; Kunst Henricus P M; Bosman Arjan J
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: van der Avoort Stijn J C; van Heerbeek Niels; Snik Ad F M; Zielhuis Gerhard A; Cremers Cor W R J
Reproducibility of sonotubometry as Eustachian tube ventilatory function test in healthy children.
International journal of pediatric otorhinolaryngology 2007;71(2):291-5.
2007: Cremers Frans P M; Kimberling William J; Külm Maigi; de Brouwer Arjan P; van Wijk Erwin; te Brinke Heleen; Cremers Cor W R J; Hoefsloot Lies H; Banfi Sandro; Simonelli Francesca; Fleischhauer Johannes C; Berger Wolfgang; Kelley Phil M; Haralambous Elene; Bitner-Glindzicz Maria; Webster Andrew R; Saihan Zubin; De Baere Elfride; Leroy Bart P; Silvestri Giuliana; McKay Gareth J; Koenekoop Robert K; Millan Jose M; Rosenberg Thomas; Joensuu Tarja; Sankila Eeva-Marja; Weil Dominique; Weston Mike D; Wissinger Bernd; Kremer Hannie
Development of a genotyping microarray for Usher syndrome.
Journal of medical genetics 2007;44(2):153-60.
2007: Pauw Robert J; Collin Rob W J; Huygen Patrick L M; Hoefsloot Lies H; Kremer Hannie; Cremers Cor W R J
Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W.
Audiology & neuro-otology 2007;12(2):77-84.
2007: Cremers C W R J
How to prevent a stapes gusher.
Advances in oto-rhino-laryngology 2007;65():278-84.
2006: Snik Ad F M; van Duijnhoven Noortje T L; Mylanus Emmanuel A M; Cremers Cor W R J
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: van der Avoort S J C; Heerbeek N van; Zielhuis G A; Cremers C W R J
Validation of sonotubometry in healthy adults.
The Journal of laryngology and otology 2006;120(10):853-6.
2006: Hendrickx Jan-Jaap; Mudde Aart H; 't Hart Leen M; Huygen Patrick L M; Cremers Cor W R J
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: Bosman Arjan J; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
Fitting range of the BAHA Cordelle.
International journal of audiology 2006;45(8):429-37.
2006: Collin Rob W J; Pauw Robert J; Schoots Jeroen; Huygen Patrick L M; Hoefsloot Lies H; Cremers Cor W R J; Kremer Hannie
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: Kunst Sylvia J W; Hol Myrthe K S; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
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: Kalay Ersan; Li Yun; Uzumcu Abdullah; Uyguner Oya; Collin Rob W; Caylan Refik; Ulubil-Emiroglu Melike; Kersten Ferry F J; Hafiz Gunter; van Wijk Erwin; Kayserili Hulya; Rohmann Edyta; Wagenstaller Janine; Hoefsloot Lies H; Strom Tim M; Nürnberg Gudrun; Baserer Nermin; den Hollander Anneke I; Cremers Frans P M; Cremers Cor W R J; Becker Christian; Brunner Han G; Nürnberg Peter; Karaguzel Ahmet; Basaran Seher; Kubisch Christian; Kremer Hannie; Wollnik Bernd
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: Plantinga Rutger F; de Brouwer Arjan P M; Huygen Patrick L M; Kunst Henricus P M; Kremer Hannie; Cremers Cor W R J
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: Pennings Ronald J E; Damen Godelieve W J A; Snik Ad F M; Hoefsloot Lies; Cremers Cor W R J; Mylanus Emmanuel A M
Audiologic performance and benefit of cochlear implantation in Usher syndrome type I.
The Laryngoscope 2006;116(5):717-22.
2006: Bischoff Anne M L C; Pennings Ronald J E; Huygen Patrick L M; Luijendijk Mirjam W; van Wijk Erwin; Cruysberg Johannes R M; Kremer Hannie; Cremers Cor W R J
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: Pauw Robert J; De Leenheer Els M R; Van Den Bogaert Kris; Huygen Patrick L M; Van Camp Guy; Joosten Frank B M; Cremers Cor W R J
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: Rohmann Edyta; Brunner Han G; Kayserili Hülya; Uyguner Oya; Nürnberg Gudrun; Lew Erin D; Dobbie Angus; Eswarakumar Veraragavan P; Uzumcu Abdullah; Ulubil-Emeroglu Melike; Leroy Jules G; Li Yun; Becker Christian; Lehnerdt Kai; Cremers Cor W R J; Yüksel-Apak Memnune; Nürnberg Peter; Kubisch Christian; Schlessinger Joseph; van Bokhoven Hans; Wollnik Bernd
Mutations in different components of FGF signaling in LADD syndrome.
Nature genetics 2006;38(4):414-7.
2006: Robertson Nahid G; Cremers Cor W R J; Huygen Patrick L M; Ikezono Tetsuo; Krastins Bryan; Kremer Hannie; Kuo Sharon F; Liberman M Charles; Merchant Saumil N; Miller Constance E; Nadol Joseph B; Sarracino David A; Verhagen Wim I M; Morton Cynthia C
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: Thomas G; Kooijman P G C; Cremers C W R J; de Jong F I C R S
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: Peters Theo A; Levtchenko Elena; Cremers Cor W R J; Curfs Jo H A J; Monnens Leo A H
No evidence of hearing loss in pseudohypoaldosteronism type 1 patients.
Acta oto-laryngologica 2006;126(3):237-9.
2006: van Wijk Erwin; van der Zwaag Bert; Peters Theo; Zimmermann Ulrike; Te Brinke Heleen; Kersten Ferry F J; Märker Tina; Aller Elena; Hoefsloot Lies H; Cremers Cor W R J; Cremers Frans P M; Wolfrum Uwe; Knipper Marlies; Roepman Ronald; Kremer Hannie
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: Plantinga Rutger F; Pennings Ronald J E; Huygen Patrick L M; Sankila Eeva-Marja; Tuppurainen Kaija; Kleemola Leenamaija; Cremers Cor W R J; Deutman August F
Visual impairment in Finnish Usher syndrome type III.
Acta ophthalmologica Scandinavica 2006;84(1):36-41.
2006: Thomas G; de Jong F I C R S; Kooijman P G C; Donders A R T; Cremers C W R J
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: Thomas G; de Jong F I C R S; Kooijman P G C; Cremers C W R J
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: Thomas George; de Jong Felix I C R S; Cremers Cor W R J; Kooijman Piet G C
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: Snik Ad F M; Mylanus Emmanuel A M; Proops David W; Wolfaardt John F; Hodgetts William E; Somers Thomas; Niparko John K; Wazen Jack J; Sterkers Olivier; Cremers Cor W R J; Tjellström Anders
Consensus statements on the BAHA system: where do we stand at present?
The Annals of otology, rhinology & laryngology. Supplement 2005;195():2-12.
2005: Kalay E; Karaguzel A; Caylan R; Heister A; Cremers F P M; Cremers C W R J; Brunner H G; de Brouwer A P M; Kremer H
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss.
Human mutation 2005;26(6):591.
2005: Kalay E; de Brouwer A P M; Caylan R; Nabuurs S B; Wollnik B; Karaguzel A; Heister J G A M; Erdol H; Cremers F P M; Cremers C W R J; Brunner H G; Kremer H
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: Cremers C W R; Kemperman M H; Bom S J H; Huygen P L M; Verhagen W I M; Kremer J M J
[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: Hol Myrthe K S; Bosman Arjan J; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
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: Kemperman Martijn H; De Leenheer Els M R; Huygen Patrick L M; van Duijnhoven Gerard; Morton Cynthia C; Robertson Nahid G; Cremers Frans P M; Kremer Hannie; Cremers Cor W R J
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: Bischoff Anne M L C; Huygen Patrick L M; Kemperman Martijn H; Pennings Ronald J E; Bom Steven J H; Verhagen Wim I M; Admiraal Ronald J C; Kremer Hannie; Cremers Cor W R J
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: de Brouwer Arjan P M; Kunst Hendrikus P M; Krebsova Alice; van Asseldonk Karin; Reis André; Snoeckx Rik L; Van Camp Guy; Cremers Cor W R J; Cremers Frans P M; Kremer Hannie
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: Hol Myrthe K S; Cremers Cor W R J; Coppens-Schellekens Wilma; Snik Ad F M
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: van der Avoort Stijn J C; van Heerbeek Niels; Zielhuis Gerhard A; Cremers Cor W R J
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: Hol Myrthe K S; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
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: Hol Myrthe K S; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
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: Plantinga R F; Kleemola L; Huygen P L M; Joensuu T; Sankila E-M; Pennings R J E; Cremers C W R J
Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients.
Audiology & neuro-otology 2005;10(2):79-89.
2005: Santos Regie Lyn P; Aulchenko Yurii S; Huygen Patrick L M; van der Donk Kim P; de Wijs Ilse J; Kemperman Martijn H; Admiraal Ronald J C; Kremer Hannie; Hoefsloot Lies H; Cremers Cor W R J
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: Topsakal Vedat; Pennings Ronald J E; te Brinke Heleen; Hamel Ben; Huygen Patrick L M; Kremer Hannie; Cremers Cor W R J
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: Weekamp H H; Kremer H; Hoefsloot L H; Kuijpers-Jagtman A M; Cruysberg J R M; Cremers C W R J
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: Baijens Laura W J; De Leenheer Els M R; Weekamp Henriëtte H; Cruysberg Johannes R M; Mortier Geert R; Cremers Cor W R J
Stickler syndrome type I and Stapes ankylosis.
International journal of pediatric otorhinolaryngology 2004;68(12):1573-80.
2004: De Leenheer Els M R; Bosman Arjan J; Kunst Hendrik P M; Huygen Patrick L M; Cremers Cor W R J
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: Peters Theo A; Monnens Leo A H; Cremers Cor W R J; Curfs Jo H A J
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: Kemperman Mathyus H; Koch Sacha M P; Kumar Shrawan; Huygen Patrick L M; Joosten Frank B M; Cremers Cor W R J
Evidence of progression and fluctuation of hearing impairment in branchio-oto-renal syndrome.
International journal of audiology 2004;43(9):523-32.
2004: Pennings Ronald J E; Topsakal Vedat; Astuto Lisa; de Brouwer Arjan P M; Wagenaar Mariette; Huygen Patrick L M; Kimberling William J; Deutman August F; Kremer Hannie; Cremers Cor W R J
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: Hol Myrthe K S; Bosman Arjan J; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
Bone-anchored hearing aid in unilateral inner ear deafness: a study of 20 patients.
Audiology & neuro-otology 2004;9(5):274-81.
2004: Pennings Ronald J E; Te Brinke Heleen; Weston Michael D; Claassen Annemarie; Orten Dana J; Weekamp Henriëtte; Van Aarem Annelies; Huygen Patrick L M; Deutman August F; Hoefsloot Lies H; Cremers Frans P M; Cremers Cor W R J; Kimberling William J; Kremer Hannie
USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.
Human mutation 2004;24(2):185.
2004: Stinckens Christel; Kremer Hannie; van Wijk Erwin; Hoefsloot Lies H; Huygen Patrick L M; Standaert Lieve; Fryns Jean Pierre; Cremers Cor W R J
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: Forton Glen E J; Cremers Cor W R J; Offeciers E Erwin
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: Luijendijk Mirjam W J; Van Wijk Erwin; Bischoff Anne M L C; Krieger Elmar; Huygen Patrick L M; Pennings Ronald J E; Brunner Han G; Cremers Cor W R J; Cremers Frans P M; Kremer Hannie
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: Snik Ad F M; Bosman Arjan J; Mylanus Emmanuel A M; Cremers Cor W R J
Candidacy for the bone-anchored hearing aid.
Audiology & neuro-otology 2004;9(4):190-6.
2004: Van Den Bogaert K; De Leenheer E M R; Chen W; Lee Y; Nürnberg P; Pennings R J E; Vanderstraeten K; Thys M; Cremers C W R J; Smith R J H; Van Camp G
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24.
Journal of medical genetics 2004;41(6):450-3.
2004: Hol Myrthe K S; Spath Marian A; Krabbe Paul F M; van der Pouw Catharina T M; Snik Ad F M; Cremers Cor W R J; Mylanus Emmanuel A M
The bone-anchored hearing aid: quality-of-life assessment.
Archives of otolaryngology--head & neck surgery 2004;130(4):394-9.
2004: Pennings Ronald J E; Huygen Patrick L M; Orten Dana J; Wagenaar Mariette; van Aarem Annelies; Kremer Hannie; Kimberling William J; Cremers Cor W R J; Deutman August F
Evaluation of visual impairment in Usher syndrome 1b and Usher syndrome 2a.
Acta ophthalmologica Scandinavica 2004;82(2):131-9.
2004: van Wijk Erwin; Pennings Ronald J E; te Brinke Heleen; Claassen Annemarie; Yntema Helger G; Hoefsloot Lies H; Cremers Frans P M; Cremers Cor W R J; Kremer Hannie
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: Snik Ad; Noten John; Cremers Cor
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: Kemperman Martijn H; De Leenheer Els M R; Huygen Patrick L M; van Wijk Erwin; van Duijnhoven Gerard; Cremers Frans P M; Kremer Hannie; Cremers Cor W R J
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: Snik A; Cremers C
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: Snoeckx R L; Kremer H; Ensink R J H; Flothmann K; de Brouwer A; Smith R J H; Cremers C W R J; Van Camp G
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: Pennings Ronald J E; Huygen Patrick L M; van den Ouweland Jody M W; Cryns Kim; Dikkeschei Lambert D; Van Camp Guy; Cremers Cor W R J
Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.
Audiology & neuro-otology 2004;9(1):51-62.
2004: Bischoff Anne M L C; Luijendijk Mirjam W J; Huygen Patrick L M; van Duijnhoven Gerard; De Leenheer Els M R; Oudesluijs Grétel G; Van Laer Lut; Cremers Frans P M; Cremers Cor W R J; Kremer Hannie
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: van Wijk E; Krieger E; Kemperman M H; De Leenheer E M R; Huygen P L M; Cremers C W R J; Cremers F P M; Kremer H
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: Pennings R J; Cryns K; Huygen P L; van Camp G; Cremers C W
[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: Nuijten Inge; Admiraal Ronald; Van Buggenhout Griet; Cremers Cor; Frijns Jean-Pierre; Smeets Dominique; van Ravenswaaij-Arts Conny
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: Cryns Kim; Sivakumaran Theru A; Van den Ouweland Jody M W; Pennings Ronald J E; Cremers Cor W R J; Flothmann Kris; Young Terry-Lynn; Smith Richard J H; Lesperance Marci M; Van Camp Guy
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: Lemaire Francois X; Feenstra Louw; Huygen Patrick L M; Fransen Erik; Devriendt Koen; Van Camp Guy; Vantrappen Greet; Cremers Cor W R J; Wackym Phillip A; Koss John C
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: Weekamp H H; Huygen P L M; Merx J L; Kremer H P H; Cremers Cor W R J; Longridge Neil S
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: van der Rijt Antoon J M; Cremers Cor W R J
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: Ensink Robbert J H; Vingerhoets H M; Schmidt C W Thijs H; Cremers Cor W R J
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: Pennings Ronald J E; Fields Randall R; Huygen Patrick L M; Deutman August F; Kimberling William J; Cremers Cor W R J
Usher syndrome type III can mimic other types of Usher syndrome.
The Annals of otology, rhinology, and laryngology 2003;112(6):525-30.
2003: van ven Ouweland Johannes M W; Cryns Kim; Pennings Ronald J E; Walraven Inge; Janssen George M C; Maassen J Antonie; Veldhuijzen Bernard F E; Arntzenius Alexander B; Lindhout Dick; Cremers Cor W R J; Van Camp Guy; Dikkeschei Lambert D
Molecular characterization of WFS1 in patients with Wolfram syndrome.
The Journal of molecular diagnostics : JMD 2003;5(2):88-95.
2003: Pennings Ronald J E; Bom Steven J H; Cryns Kim; Flothmann Kris; Huygen Patrick L M; Kremer Hannie; Van Camp Guy; Cremers Cor W R J
Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
Archives of otolaryngology--head & neck surgery 2003;129(4):421-6.
2003: Bom Steven J H; Kemperman Martijn H; Huygen Patrick L M; Luijendijk Mirjam W J; Cremers Cor W R J
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: De Leenheer Els M R; Oudesluijs Grétel G; Kuijpers-Jagtman Anne-Marie; Rappold Gudrun A; Sengers Rob C A; Cremers Cor W R J
Congenital conductive hearing loss in dyschondrosteosis.
The Annals of otology, rhinology, and laryngology 2003;112(2):153-8.
2003: de Brouwer Arjan P M; Pennings Ronald J E; Roeters Marjolijn; Van Hauwe Peter; Astuto Lisa M; Hoefsloot Lies H; Huygen Patrick L M; van den Helm Bellinda; Deutman August F; Bork Julie M; Kimberling William J; Cremers Frans P M; Cremers Cor W R J; Kremer Hannie
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: Bosman Arjan J; Hol Myrthe K S; Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
Bone-anchored hearing aids in unilateral inner ear deafness.
Acta oto-laryngologica 2003;123(2):258-60.
2003: Pennings Ronald J E; Huygen Patrick L M; Weston Michael D; van Aarem Annelies; Wagenaar Mariette; Kimberling William J; Cremers Cor W R J
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: van Heerbeek Niels; Tonnaer Edith L G M; Ingels Koen J A O; Curfs Jo H A J; Cremers Cor W R J
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.
2003: Vantrappen G; Rommel N; Swillen A; Cremers C W; Fryns J P; Devriendt K
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.
Acta oto-rhino-laryngologica Belgica 2003;57(2):101-6.
2002: Pennings R J E; Kremer H; Deutman A F; Kimberling W J; Cremers C W R J
[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: Mylanus Emmanuel A M; Johansson Carina B; Cremers Cor W R J
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: Bom Steven J H; Van Camp Guy; Cryns Kim; Admiraal Ronald J C; Huygen Patrick L M; Cremers Cor W R J
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: Kemperman Martijn H; Koch Sacha M P; Joosten Frank B M; Kumar Shrawan; Huygen Patrick L M; Cremers Cor W R J
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: Cremers C W R J; De Mönnink J P; Arts N; Joosten F B M; Kremer H; Hoefsloot L
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: Astuto L M; Bork J M; Weston M D; Askew J W; Fields R R; Orten D J; Ohliger S J; Riazuddin S; Morell R J; Khan S; Riazuddin S; Kremer H; van Hauwe P; Moller C G; Cremers C W R J; Ayuso C; Heckenlively J R; Rohrschneider K; Spandau U; Greenberg J; Ramesar R; Reardon W; Bitoun P; Millan J; Legge R; Friedman T B; Kimberling W J
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: De Leenheer Els M R; van Zuijlen Diederick A; Van Laer Lut; Van Camp Guy; Huygen Patrick L M; Huizing Egbert H; Cremers Cor W R J
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: Van Camp Guy; Coucke Paul J; Akita Jiro; Fransen Erik; Abe Satoko; De Leenheer Els M R; Huygen Patrick L M; Cremers Cor W R J; Usami Shin-Ichi
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.
Human mutation 2002;20(1):15-9.
2002: Cryns Kim; Pfister Markus; Pennings Ronald J E; Bom Steven J H; Flothmann Kris; Caethoven Goele; Kremer Hannie; Schatteman Isabelle; Köln Karen A; Tóth Tímea; Kupka Susan; Blin Nikolaus; Nürnberg Peter; Thiele Holger; van de Heyning Paul H; Reardon William; Stephens Dafydd; Cremers Cor W R J; Smith Richard J H; Van Camp Guy
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: Pennings R J E; Dikkeschei L D; Cremers C W R J; van den Ouweland J M W
[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: Kemperman Martijn H; Hoefsloot Lies H; Cremers Cor W R J
Hearing loss and connexin 26.
Journal of the Royal Society of Medicine 2002;95(4):171-7.
2002: Van Den Bogaert K; Govaerts P J; De Leenheer E M R; Schatteman I; Verstreken M; Chen W; Declau F; Cremers C W R J; Van De Heyning P H; Offeciers F E; Somers T; Smith R J H; Van Camp G
Otosclerosis: a genetically heterogeneous disease involving at least three different genes.
Bone 2002;30(4):624-30.
2002: Vantrappen Greet; Rommel Nathalie; Cremers Cor W R J; Fryns Jean-Pierre; Devriendt Koen
Mosaic trisomy 8 as a cause of velopharyngeal insufficiency.
American journal of medical genetics 2002;108(4):337-8.
2002: Peters Theo A; Tonnaer Edith L G M; Kuijpers Wim; Cremers Cor W R J; Curfs Jo H A J
Differences in endolymphatic sac mitochondria-rich cells indicate specific functions.
The Laryngoscope 2002;112(3):534-41.
2002: De Leenheer Els M R; Huygen Patrick L M; Coucke Paul J; Admiraal Ronald J C; van Camp G; Cremers Cor W
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: Ceruti S; Stinckens C; Cremers C W R J; Casselman J W
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: Cremers C W R J
Surgery for acquired atresia of the external ear canal.
Clinical otolaryngology and allied sciences 2002;27(1):75-6.
2002: Hoefsloot L H; Kemperman M; Cremers C W R J
[From gene to disease: deafness and connexin 26]
Nederlands tijdschrift voor geneeskunde 2002;146(6):259-61.
2002: Vantrappen G; Rommel N; Wellens W; Cremers C W R J; Fryns J-P; Devriendt K
Autosomal dominant isolated velopharyngeal insufficiency.
Clinical genetics 2002;61(1):74-6.
2002: Snik Ad F M; Mylanus Emmanuel A M; Cremers Cor W R J
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.
2002: Kemperman M H; Stinckens C; Kumar S; Joosten F B M; Huygen P L M; Cremers C W R J
The branchio-oto-renal syndrome.
Advances in oto-rhino-laryngology 2002;61():192-200.
2002: Pennings R J E; Wagenaar M; van Aarem A; Huygen P L M; Kimberling W J; Cremers C W R J
Hearing impairment in Usher's syndrome.
Advances in oto-rhino-laryngology 2002;61():184-91.
2002: Ensink Robbert J H; Huygen Patrick L M; Cremers Cor W R J
The clinical spectrum of maternally transmitted hearing loss.
Advances in oto-rhino-laryngology 2002;61():172-83.
2002: Cremers C W R J; Snik A F M; Huygen P L M; Joosten F B M; Cremers F P M
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: Stinckens C; Huygen P L M; Van Camp G; Cremers C W R J
Pendred syndrome redefined. Report of a new family with fluctuating and progressive hearing loss.
Advances in oto-rhino-laryngology 2002;61():131-41.
2002: Huygen Patrick L M; Bom Steven J H; Van Camp Guy; Cremers Cor W R J
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: De Leenheer Els M R; McGuirt Wyman T; Kunst Henricus P M; Huygen Patrick L M; Smith Richard J H; Cremers Cor W R J
The phenotype of DFNA13/COL11A2.
Advances in oto-rhino-laryngology 2002;61():85-91.
2002: De Leenheer Els M R; Huygen Patrick L M; Wayne Sigrid; Verstreken Margriet; Declau Frank; Van Camp Guy; Van de Heyning Paul H; Smith Richard J H; Cremers Cor W R J
DFNA10/EYA4--the clinical picture.
Advances in oto-rhino-laryngology 2002;61():73-8.
2002: Kemperman Martijn H; Bom Steven J H; Lemaire François X; Verhagen Wim I M; Huygen Patrick L M; Cremers Cor W R J
DFNA9/COCH and its phenotype.
Advances in oto-rhino-laryngology 2002;61():66-72.
2002: De Leenheer Els M R; van Zuijlen Diederick A; Van Laer Lut; Van Camp Guy; Huygen Patrick L M; Huizing Egbert H; Cremers Cor W R J
Clinical features of DFNA5.
Advances in oto-rhino-laryngology 2002;61():53-9.
2002: De Leenheer Els M R; Ensink Robbert J H; Kunst Henricus P M; Marres Henri A M; Talebizadeh Zohreh; Declau Frank; Smith Shelley D; Usami Shin-ichi; Van de Heyning Paul H; Van Camp Guy; Huygen Patrick L M; Cremers Cor W R J
DFNA2/KCNQ4 and its manifestations.
Advances in oto-rhino-laryngology 2002;61():41-6.
2001: Verhagen W I; Bom S J; Fransen E; Van Camp G; Huygen P L; Theunissen E J; Cremers C W
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: Snik A F; Cremers C W
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: Stinckens C; Huygen P L; Joosten F B; Van Camp G; Otten B; Cremers C W
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: Bespalova I N; Van Camp G; Bom S J; Brown D J; Cryns K; DeWan A T; Erson A E; Flothmann K; Kunst H P; Kurnool P; Sivakumaran T A; Cremers C W; Leal S M; Burmeister M; Lesperance M M
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: Kemperman M H; Stinckens C; Kumar S; Huygen P L; Joosten F B; Cremers C W
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: De Leenheer E M; Huygen P L; Wayne S; Smith R J; Cremers C W
The DFNA10 phenotype.
The Annals of otology, rhinology, and laryngology 2001;110(9):861-6.
2001: Bom S J; De Leenheer E M; Lemaire F X; Kemperman M H; Verhagen W I; Marres H A; Kunst H P; Ensink R J; Bosman A J; Van Camp G; Cremers F P; Huygen P L; Cremers C W
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: Ensink R J; Huygen P L; Snoeckx R L; Caethoven G; Van Camp G; Cremers C W
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: Stinckens C; Standaert L; Casselman J W; Huygen P L; Kumar S; Van de Wallen J; Cremers C W
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: Bosman A J; Snik A F; van der Pouw C T; Mylanus E A; Cremers C W
Audiometric evaluation of bilaterally fitted bone-anchored hearing aids.
Audiology : official organ of the International Society of Audiology 2001;40(3):158-67.
2001: Peters T A; Tonnaer E L; Kuijpers W; Cremers C W; Curfs J H
Developmental aspects of the rat endolymphatic sac and functional implications.
Acta oto-laryngologica 2001;121(2):125-9.
2001: Fransen E; Verstreken M; Bom S J; Lemaire F; Kemperman M H; De Kok Y J; Wuyts F L; Verhagen W I; Huygen P L; McGuirt W T; Smith R J; Van Maldergem L V; Declau F; Cremers C W; Van De Heyning P H; Cremers F P; Van Camp G
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: van der Mey A G; Malessy M J; Frijns J H; Grooters E; Cremers C W; Graamans K; Grotenhuis J A; Mulder J J
[Stereotaxic irradiation of vestibular schwannoma (acoustic neurinoma)]
Nederlands tijdschrift voor geneeskunde 2001;145(4):196-7.
2001: De Leenheer E M; Kunst H H; McGuirt W T; Prasad S D; Brown M R; Huygen P L; Smith R J; Cremers C W
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).
Archives of otolaryngology--head & neck surgery 2001;127(1):13-7.
2001: Vantrappen G; Rommel N; Devriendt K; Cremers C W; Feenstra L; Fryns J P
Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Acta oto-rhino-laryngologica Belgica 2001;55(1):43-8.
2000: Astuto L M; Weston M D; Carney C A; Hoover D M; Cremers C W; Wagenaar M; Moller C; Smith R J; Pieke-Dahl S; Greenberg J; Ramesar R; Jacobson S G; Ayuso C; Heckenlively J R; Tamayo M; Gorin M B; Reardon W; Kimberling W J
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
American journal of human genetics 2000;67(6):1569-74.
2000: Wagenaar M; Schuknecht H; Nadol J; Benraad-Van Rens M; Pieke-Dahl S; Kimberling W; Cremers C
Histopathologic features of the temporal bone in usher syndrome type I.
Archives of otolaryngology--head & neck surgery 2000;126(8):1018-23.
2000: Van Hauwe P; Coucke P J; Ensink R J; Huygen P; Cremers C W; Van Camp G
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: Verhagen W I; Bom S J; Huygen P L; Fransen E; Van Camp G; Cremers C W
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9).
Archives of neurology 2000;57(7):1045-7.
2000: Koch S M; Kumar S; Cremers C W
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: Kumar S; Deffenbacher K; Marres H A; Cremers C W; Kimberling W J
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: Pieke-Dahl S; Möller C G; Kelley P M; Astuto L M; Cremers C W; Gorin M B; Kimberling W J
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.
Journal of medical genetics 2000;37(4):256-62.
2000: Weston M D; Eudy J D; Fujita S; Yao S; Usami S; Cremers C; Greenberg J; Ramesar R; Martini A; Moller C; Smith R J; Sumegi J; Kimberling W J;
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: Kunst H; Huybrechts C; Marres H; Huygen P; Van Camp G; Cremers C
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: Admiraal R J; Brunner H G; Dijkstra T L; Huygen P L; Cremers C W
Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.
The Laryngoscope 2000;110(3 Pt 1):457-61.
2000: Kunst H; Marres H; Huygen P; van Duijnhoven G; Krebsova A; van der Velde S; Reis A; Cremers F; Cremers C
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: Cremers C W
Hearing: cracking the code.
The Journal of laryngology and otology 2000;114(1):6-16.
2000: Orten D J; Weston M D; Kelley P M; Cremers C W; Wagenaar M; Jacobson S G; Kimberling W J
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.
Human mutation 2000;15(1):114-5.
2000: Cremers F P; Cremers C W; Ropers H H
The ins and outs of X-linked deafness type 3.
Advances in oto-rhino-laryngology 2000;56():184-95.
2000: Ensink R J; Huygen P L; Van Hauwe P; Coucke P; Cremers C W; Van Camp G
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.
1999: McGuirt W T; Prasad S D; Griffith A J; Kunst H P; Green G E; Shpargel K B; Runge C; Huybrechts C; Mueller R F; Lynch E; King M C; Brunner H G; Cremers C W; Takanosu M; Li S W; Arita M; Mayne R; Prockop D J; Van Camp G; Smith R J
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).
Nature genetics 1999;23(4):413-9.
1999: Wagenaar M; Draaijer P; Meek H; ten Donkelaar H J; Wesseling P; Kimberling W; Cremers C
The cochlear nuclei in two patients with Usher syndrome type I.
International journal of pediatric otorhinolaryngology 1999;50(3):185-95.
1999: Snik A F; Cremers C W
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: Bom S J; Kunst H P; Huygen P L; Cremers F P; Cremers C W
Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.
British journal of audiology 1999;33(5):335-48.
1999: Declau F; Cremers C; Van de Heyning P
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: Orten D J; Weston M D; Kelley P M; Cremers C W; Wagenaar M; Jacobson S G; Kimberling W J
Analysis of DNA elements that modulate myosin VIIA expression in humans.
Human mutation 1999;14(4):354.
1999: Bom S J; Kemperman M H; De Kok Y J; Huygen P L; Verhagen W I; Cremers F P; Cremers C W
Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9.
The Laryngoscope 1999;109(9):1525-30.
1999: Van Camp G; Kunst H; Flothmann K; McGuirt W; Wauters J; Marres H; Verstreken M; Bespalova I N; Burmeister M; Van de Heyning P H; Smith R J; Willems P J; Cremers C W; Lesperance M M
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: Coucke P J; Van Hauwe P; Kelley P M; Kunst H; Schatteman I; Van Velzen D; Meyers J; Ensink R J; Verstreken M; Declau F; Marres H; Kastury K; Bhasin S; McGuirt W T; Smith R J; Cremers C W; Van de Heyning P; Willems P J; Smith S D; Van Camp G
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
Human molecular genetics 1999;8(7):1321-8.
1999: van der Pouw C T; Snik A F; Cremers C W
The BAHA HC200/300 in comparison with conventional bone conduction hearing aids.
Clinical otolaryngology and allied sciences 1999;24(3):171-6.
1999: van der Pouw C T; Mylanus E A; Cremers C W
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: Kunst H; Marres H; Huygen P; Van Camp G; Joosten F; Cremers C
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: Ensink R J; Sleeckx J P; Cremers C W
Proximal symphalangism and congenital conductive hearing loss: otologic aspects.
The American journal of otology 1999;20(3):344-9.
1999: van Aarem A; Wagenaar M; Tonnaer E; Pieke Dahl S; Bisseling J; Janssen H; Bastiaans B; Kimberling W; Cremers C
Semen analysis in the Usher syndrome type 2A.
ORL; journal for oto-rhino-laryngology and its related specialties 1999;61(3):126-30.
1999: Wagenaar M; van Aarem A; Huygen P; Pieke-Dahl S; Kimberling W; Cremers C
Hearing impairment related to age in Usher syndrome types 1B and 2A.
Archives of otolaryngology--head & neck surgery 1999;125(4):441-5.
1999: Van Hauwe P; Coucke P J; Declau F; Kunst H; Ensink R J; Marres H A; Cremers C W; Djelantik B; Smith S D; Kelley P; Van de Heyning P H; Van Camp G
Deafness linked to DFNA2: one locus but how many genes?
Nature genetics 1999;21(3):263.
1999: de Kok Y J; Bom S J; Brunt T M; Kemperman M H; van Beusekom E; van der Velde-Visser S D; Robertson N G; Morton C C; Huygen P L; Verhagen W I; Brunner H G; Cremers C W; Cremers F P
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: Verhoeven K; Ensink R J; Tiranti V; Huygen P L; Johnson D F; Schatteman I; Van Laer L; Verstreken M; Van de Heyning P; Fischel-Ghodsian N; Zeviani M; Cremers C W; Willems P J; Van Camp G
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: Vantrappen G; Rommel N; Cremers C W; Devriendt K; Frijns J P
The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.
International journal of pediatric otorhinolaryngology 1998;45(2):133-41.
1998: Cremers C W; Admiraal R J; Huygen P L; Bolder C; Everett L A; Joosten F B; Green E D; van Camp G; Otten B J
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: Snik A F; Mylanus E A; Cremers C W
Implantable hearing devices for sensorineural hearing loss: a review of the audiometric data.
Clinical otolaryngology and allied sciences 1998;23(5):414-9.
1998: Ensink R J; Verhoeven K; Marres H A; Huygen P L; Padberg G W; ter Laak H; van Camp G; Willems P J; Cremers C W
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: Van Hauwe P; Everett L A; Coucke P; Scott D A; Kraft M L; Ris-Stalpers C; Bolder C; Otten B; de Vijlder J J; Dietrich N L; Ramesh A; Srisailapathy S C; Parving A; Cremers C W; Willems P J; Smith R J; Green E D; Van Camp G
Two frequent missense mutations in Pendred syndrome.
Human molecular genetics 1998;7(7):1099-104.
1998: Eudy J D; Weston M D; Yao S; Hoover D M; Rehm H L; Ma-Edmonds M; Yan D; Ahmad I; Cheng J J; Ayuso C; Cremers C; Davenport S; Moller C; Talmadge C B; Beisel K W; Tamayo M; Morton C C; Swaroop A; Kimberling W J; Sumegi J
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: Kumar S; Marres H A; Cremers C W; Kimberling W J
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: van der Pouw K T; Snik A F; Cremers C W
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: Mylanus E A; van der Pouw K C; Snik A F; Cremers C W
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: Snik A F; Beynon A J; Mylanus E A; van der Pouw C T; Cremers C W
Binaural application of the bone-anchored hearing aid.
The Annals of otology, rhinology, and laryngology 1998;107(3):187-93.
1998: van Aarem A; Muytjens H L; Smits M M; Cremers C W
Recurrent therapy resistant mastoiditis by Mycobacterium cheilonae abscessus, a nontuberculous mycobacterium.
International journal of pediatric otorhinolaryngology 1998;43(1):61-72.
1998: Kunst H; Marres H; Van Camp G; Cremers C
Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research.
Clinical otolaryngology and allied sciences 1998;23(1):9-17.
1998: Ensink R J; Camp G V; Cremers C W
Mitochondrial inherited hearing loss.
Clinical otolaryngology and allied sciences 1998;23(1):3-8.
1998: van der Pouw C T; Johansson C B; Mylanus E A; Albrektsson T; Cremers C W
Removal of titanium implants from the temporal bone: histologic findings.
The American journal of otology 1998;19(1):46-51.
1998: Kunst H; Marres H; Huygen P; Ensink R; Van Camp G; Van Hauwe P; Coucke P; Willems P; Cremers C
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2.
The Laryngoscope 1998;108(1 Pt 1):74-80.
1998: van der Pouw C T; Carlsson P; Cremers C W; Snik A F
A new more powerful bone-anchored hearing aid: first results.
Scandinavian audiology 1998;27(3):179-82.
1998: Kumar S; Kimberling W J; Weston M D; Schaefer B G; Berg M A; Marres H A; Cremers C W
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome.
Human mutation 1998;11(6):443-9.
1998: Hol F A; Geurds M P; Cremers C W; Hamel B C; Mariman E C
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.
1997: Marres H; van Ewijk M; Huygen P; Kunst H; van Camp G; Coucke P; Willems P; Cremers C
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: Van Camp G; Coucke P J; Kunst H; Schatteman I; Van Velzen D; Marres H; van Ewijk M; Declau F; Van Hauwe P; Meyers J; Kenyon J; Smith S D; Smith R J; Djelantik B; Cremers C W; Van de Heyning P H; Willems P J
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: Struycken P M; Cremers C W; Mariman E C; Joosten F B; Bleker R J
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: Coucke P; Van Camp G; Demirhan O; Kabakkaya Y; Balemans W; Van Hauwe P; Van Agtmael T; Smith R J; Parving A; Bolder C H; Cremers C W; Willems P J
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: Stinckens C; Ensink R; Feenstra L; Fryns J P; Cremers C
Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes.
International journal of pediatric otorhinolaryngology 1997;38(3):237-45.
1997: Ensink R J; Cremers C W; Brunner H G
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome.
Archives of otolaryngology--head & neck surgery 1997;123(1):97-9.
1997: Kumar S; Deffenbacher K; Cremers C W; Van Camp G; Kimberling W J
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: Ensink R J; Brunner H G; Cremers C W
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: de Kok Y J; Cremers C W; Ropers H H; Cremers F P
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.
1996: van Aarem A; Pinckers A J; Kimberling W J; Huygen P L; Bleeker-Wagemakers E M; Cremers C W
Stable and progressive hearing loss in type 2A Usher's syndrome.
The Annals of otology, rhinology, and laryngology 1996;105(12):962-7.
1996: Wagenaar M; Snik A F; Kimberling W J; Cremers C W
Carriers of the Usher syndrome type IB: is audiometric identification possible?
The American journal of otology 1996;17(6):853-8.
1996: Weston M D; Kelley P M; Overbeck L D; Wagenaar M; Orten D J; Hasson T; Chen Z Y; Corey D; Mooseker M; Sumegi J; Cremers C; Moller C; Jacobson S G; Gorin M B; Kimberling W J
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
American journal of human genetics 1996;59(5):1074-83.
1996: Ensink R J; Marres H A; Brunner H G; Cremers C W
Hearing loss in the Saethre-Chotzen syndrome.
The Journal of laryngology and otology 1996;110(10):952-7.
1996: Huygen P L; Cremers C W; Verhagen W I; Joosten F B
Camurati-Engelmann disease presenting as 'juvenile otosclerosis'.
International journal of pediatric otorhinolaryngology 1996;37(2):129-41.
1996: Pieke-Dahl S; van Aarem A; Dobin A; Cremers C W; Kimberling W J
Genetic heterogeneity of Usher syndrome type II in a Dutch population.
Journal of medical genetics 1996;33(9):753-7.
1996: de Kok Y J; Vossenaar E R; Cremers C W; Dahl N; Laporte J; Hu L J; Lacombe D; Fischel-Ghodsian N; Friedman R A; Parnes L S; Thorpe P; Bitner-Glindzicz M; Pander H J; Heilbronner H; Graveline J; den Dunnen J T; Brunner H G; Ropers H H; Cremers F P
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: van Leeuwen J P; Braspenning J C; Meijer H; Cremers C W
Quality of life after acoustic neuroma surgery.
The Annals of otology, rhinology, and laryngology 1996;105(6):423-30.
1996: van Leeuwen J P; Harhangi B S; Thewissen N P; Thijssen H O; Cremers C W
Delays in the diagnosis of acoustic neuromas.
The American journal of otology 1996;17(2):321-5.
1996: Kumar S; Kimberling W J; Lanyi A; Sumegi J; Pinnt J; Ing P; Tinley S; Marres H A; Cremers C W
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: Van Aarem A; Wagenaar M; Pinckers A J; Huygen P L; Bleeker-Wagemakers E M; Kimberling B J; Cremers C W
Ophthalmologic findings in Usher syndrome type 2A.
Ophthalmic genetics 1995;16(4):151-8.
1995: van Leeuwen J P; Pruszczynski M; Marres H A; Grotenhuis J A; Cremers C W
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: van Vierzen P B; Joosten F B; Marres H A; Cremers C W; Ruijs J H
Mandibulofacial dysostosis: CT findings of the temporal bones.
European journal of radiology 1995;21(1):53-7.
1995: Wagenaar M; ter Rahe B; van Aarem A; Huygen P; Admiraal R; Bleeker-Wagemakers E; Pinckers A; Kimberling W; Cremers C
Clinical findings in obligate carriers of type I Usher syndrome.
American journal of medical genetics 1995;59(3):375-9.
1995: Chen A; Francis M; Ni L; Cremers C W; Kimberling W J; Sato Y; Phelps P D; Bellman S C; Wagner M J; Pembrey M
Phenotypic manifestations of branchio-oto-renal syndrome.
American journal of medical genetics 1995;58(4):365-70.
1995: van Leeuwen J P; Cremers C W; Thewissen N P; Harhangi B S; Meijer E
Acoustic neuroma: correlation among tumor size, symptoms, and patient age.
The Laryngoscope 1995;105(7 Pt 1):701-7.
1995: Cremers C W; Strübbe E H; Willemsen W N
Stapedial ankylosis in the Mayer-Rokitansky-Küster-Hauser syndrome.
Archives of otolaryngology--head & neck surgery 1995;121(7):800-3.
1995: Cremers C W; Brown S D; Steel K P; Brunner H G; Read A P; Kimberling W J
Gene linkage and genetic deafness.
International journal of pediatric otorhinolaryngology 1995;32 Suppl():S167-74.
1995: Marres H A; Cremers C W; Dixon M J; Huygen P L; Joosten F B
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: Mylanus E A; Snik A F; Cremers C W
Patients' opinions of bone-anchored vs conventional hearing aids.
Archives of otolaryngology--head & neck surgery 1995;121(4):421-5.
1995: Snik A F; Hombergen G C; Mylanus E A; Cremers C W
Air-bone gap in patients with X-linked stapes gusher syndrome.
The American journal of otology 1995;16(2):241-6.
1995: van Aarem A; Cremers C W; Pinckers A J; Huygen P L; Hombergen G C; Kimberling B J
The Usher syndrome type 2A: clinical findings in obligate carriers.
International journal of pediatric otorhinolaryngology 1995;31(2-3):159-74.
1995: Snik A F; Mylanus E A; Cremers C W
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: Snik A F; Mylanus E A; Cremers C W
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: Marres H A; Cremers C W; Marres E H; Huygen P L
Ear surgery in Treacher Collins syndrome.
The Annals of otology, rhinology, and laryngology 1995;104(1):31-41.
1995: Kimberling W J; Weston M D; Möller C; van Aarem A; Cremers C W; Sumegi J; Ing P S; Connolly C; Martini A; Milani M
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: Mariman E C; van Beersum S E; Cremers C W; Struycken P M; Ropers H H
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: Kumar S; Kimberling W J; Connolly C J; Tinley S; Marres H A; Cremers C W
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: Van Leeuwen J P; Cremers C W; Theunissen E J; Marres E H; Meyer E
Translabyrinthine and transotic surgery for acoustic neuroma.
Clinical otolaryngology and allied sciences 1994;19(6):491-5.
1994: Mylanus E A; Cremers C W
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: Snik A F; Mylanus E A; Cremers C W
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: Cremers C W; van Rijn P M; Huygen P L
The sex-ratio in childhood deafness, an analysis of the male predominance.
International journal of pediatric otorhinolaryngology 1994;30(2):105-10.
1994: Coucke P; Van Camp G; Djoyodiharjo B; Smith S D; Frants R R; Padberg G W; Darby J K; Huizing E H; Cremers C W; Kimberling W J
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: Mylanus E A; Beynon A J; Snik A F; Cremers C W
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: Strübbe E H; Cremers C W; Dikkers F G; Willemsen W N
Hearing loss and the Mayer-Rokitansky-Küster-Hauser syndrome.
The American journal of otology 1994;15(3):431-6.
1994: Mylanus E A; Snik F M; Cremers C W; Jorritsma F F; Verschuure H
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: Mylanus E A; Snik A F; Jorritsma F F; Cremers C W
Audiologic results for the bone-anchored hearing aid HC220.
Ear and hearing 1994;15(1):87-92.
1994: Snik A F; Mylanus E A; Cremers C W
Speech recognition with the bone-anchored hearing aid determined objectively and subjectively.
Ear, nose, & throat journal 1994;73(2):115-7.
1994: Mylanus E A; Cremers C W; Snik A F; van den Berge N W
Clinical results of percutaneous implants in the temporal bone.
Archives of otolaryngology--head & neck surgery 1994;120(1):81-5.
1994: von Bokhoven H; von Genderen C; Molloy C M; van de Pol D J; Cremers C W; von Aarem A; Schwartz M; Rosenberg T; Geurts van Kessel A H; Ropers H H
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: Marres H A; Cremers C W; Huygen P L; Joosten F B
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: Mylanus E A; Snik A F; Cremers C W
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: Cremers C W; Marres H A; Brunner H G
Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndrome.
The Laryngoscope 1993;103(10):1186-9.
1993: Mariman E C; van Beersum S E; Cremers C W; van Baars F M; Ropers H H
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: van Leeuwen J P; Cremers C W; Thijssen H O; Meyer H E
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: Huygen P L; van Rijn P M; Cremers C W; Theunissen E J
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: Teunissen E; Cremers C W
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: Kumar S; Kimberling W J; Kenyon J B; Smith R J; Marres H A; Cremers C W
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: Bach I; Brunner H G; Beighton P; Ruvalcaba R H; Reardon W; Pembrey M E; van der Velde-Visser S D; Bruns G A; Cremers C W; Cremers F P
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3).
American journal of human genetics 1992;51(1):38-44.
1992: Cremers C W; Snik F M; Beynon A J
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: Cremers C W; van der Burgt C J
Hearing loss in Noonan syndrome.
International journal of pediatric otorhinolaryngology 1992;23(1):81-4.
1992: Snik A F; Jorritsma F F; Cremers C W; Beynon A J; van den Berge N W
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: Cremers C W; Beusen J M; Huygen P L
Hearing gain after stapedotomy, partial platinectomy, or total stapedectomy for otosclerosis.
The Annals of otology, rhinology, and laryngology 1991;100(12):959-61.
1991: Marres H A; Cremers C W
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: Cremers C W; Teunissen E
The impact of a syndromal diagnosis on surgery for congenital minor ear anomalies.
International journal of pediatric otorhinolaryngology 1991;22(1):59-74.
1991: Teunissen B; Cremers C W
Surgery for congenital stapes ankylosis with an associated congenital ossicular chain anomaly.
International journal of pediatric otorhinolaryngology 1991;21(3):217-26.
1991: Cremers C W; Snik A F; Beynon A J
[A hearing aid anchored in the cranial bone for amplification of bone conduction]
Nederlands tijdschrift voor geneeskunde 1991;135(11):468-71.
1991: Garretsen T J; Cremers C W
Stapes surgery in osteogenesis imperfecta: analysis of postoperative hearing loss.
The Annals of otology, rhinology, and laryngology 1991;100(2):120-30.
1991: Comeau K; Kimberling W J; Cremers C W; Shugart Y
The search for branchiootorenal syndrome on chromosomes 1 and 8.
Annals of the New York Academy of Sciences 1991;630():288-9.
1991: Garretsen T J; Cremers C W
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: Cremers C W; van Rijn P M
Acquired causes of deafness in childhood.
Annals of the New York Academy of Sciences 1991;630():197-202.
1991: Cremers C W; Marres H A; van Rijn P M
Nonsyndromal profound genetic deafness in childhood.
Annals of the New York Academy of Sciences 1991;630():191-6.
1991: Brunner H G; Smeets B; Smeets D; Nelen M; Cremers C W; Ropers H H
Molecular genetics of X-linked hearing impairment.
Annals of the New York Academy of Sciences 1991;630():176-90.
1990: Garretsen T J; Cremers C W
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: Cremers C; Garretsen T
Stapes surgery in osteogenesis imperfecta.
The American journal of otology 1989;10(6):474-6.
1989: Marres H A; Cremers C W; Jongbloet P H
Hearing levels in the Cornelia de Lange syndrome. A report of seven cases.
International journal of pediatric otorhinolaryngology 1989;18(1):31-7.
1989: Cremers C W; van Rijn P M; Hageman M J
Prevention of serious hearing impairment of deafness in the young child.
Journal of the Royal Society of Medicine 1989;82(8):484-7.
1989: Marres H A; Cremers C W
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: Cremers C W; Delleman W J
Usher's syndrome, temporal bone pathology.
International journal of pediatric otorhinolaryngology 1988;16(1):23-30.
1988: van Rijn P M; Cremers C W
Surgery for congenital conductive deafness in Klippel-Feil syndrome.
The Annals of otology, rhinology, and laryngology 1988;97(4 Pt 1):347-52.
1988: Cremers C W; Teunissen E; Marres E H
Classification of congenital aural atresia and results of reconstructive surgery.
Advances in oto-rhino-laryngology 1988;40():9-14.
1987: Cremers C; van Rijn P; ter Haar B
Autosomal recessive progressive high-frequency sensorineural deafness in childhood.
Archives of otolaryngology--head & neck surgery 1987;113(12):1319-24.
1987: Cremers C W; Hageman M J; van Rijn P M
[Prevention of severe hard-of-hearing or deafness in young children]
Nederlands tijdschrift voor geneeskunde 1987;131(17):703-6.
1987: Cremers C W; Marres E H
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: Cremers C W; Hombergen G C; Scaf J J; Huygen P L; Volkers W S; Pinckers A J
X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery.
Archives of otolaryngology (Chicago, Ill. : 1960) 1985;111(4):249-54.

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