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Robbert Ensink

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A A Tieleman; S Knuijt; J van Vliet; B J M de Swart; Robbert J H Ensink; B G M van Engelen
Dysphagia is present but mild in myotonic dystrophy type 2.
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.
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.

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All Publications

2009: A A Tieleman; S Knuijt; J van Vliet; B J M de Swart; Robbert J H Ensink; B G M van Engelen
Dysphagia is present but mild in myotonic dystrophy type 2.
Neuromuscular disorders : NMD 2009;19(3):196-8.
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.
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.
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: 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.
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.
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: 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.
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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.