Prevalence and causes of hearing impairment in Africa
Mulwafu, W., Kuper, H., Ensink, R. J. H.
Published in Tropical medicine & international health (01.02.2016)
Published in Tropical medicine & international health (01.02.2016)
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Journal Article
Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families
Coucke, Paul J., Van Hauwe, Peter, Kelley, Philip M., Kunst, Henricus, Schatteman, Isabelle, Van Velzen, Désirée, Meyers, Johan, Ensink, Robbert J., Verstreken, Margriet, Declau, Frank, Marres, Henri, Kastury, Kumar, Bhasin, Shalender, McGuirt, Wyman T., Smith, Richard J. H., Cremers, Cor W.R.J., Van de Heyning, Paul, Willems, Patrick J., Smith, Shelley D., Van Camp, Guy
Published in Human molecular genetics (01.07.1999)
Published in Human molecular genetics (01.07.1999)
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Journal Article
A congenital mucocele of the anterior dorsal tongue
Wong Chung, J.E.R.E, Ensink, R.J.H, Thijs, H.F.H, van den Hoogen, F.J.A
Published in International journal of pediatric otorhinolaryngology (01.07.2014)
Published in International journal of pediatric otorhinolaryngology (01.07.2014)
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Journal Article
Deafness linked to DFNA2: one locus but how many genes?
Camp, Guy Van, Hauwe, Peter Van, Coucke, Paul J, Declau, Frank, Kunst, Henricus, Ensink, Robbert J, Marres, Henri A, Cremers, Cor W.R.J, Djelantik, Bulantrisna, Smith, Shelley D, Kelley, Phil, Heyning, Paul H. Van de
Published in Nature genetics (01.03.1999)
Published in Nature genetics (01.03.1999)
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Journal Article
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region
ENSINK, R. J. H, HUYGEN, P. L. M, VAN HAUWE, P, COUCKE, P, CREMERS, C. W. R. J, VAN CAMP, G
Published in European archives of oto-rhino-laryngology (2000)
Published in European archives of oto-rhino-laryngology (2000)
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Conference Proceeding
Journal Article
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3
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
Published in Journal of medical genetics (01.01.2004)
Published in Journal of medical genetics (01.01.2004)
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Journal Article
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome
Ensink, R J, Cremers, C W, Brunner, H G
Published in Archives of otolaryngology--head & neck surgery (01.01.1997)
Published in Archives of otolaryngology--head & neck surgery (01.01.1997)
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Journal Article
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region
Van Hauwe, P, Coucke, P J, Ensink, R J, Huygen, P, Cremers, C W, Van Camp, G
Published in American journal of medical genetics (31.07.2000)
Published in American journal of medical genetics (31.07.2000)
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Journal Article
Proximal symphalangism and congenital conductive hearing loss: otologic aspects
Ensink, R J, Sleeckx, J P, Cremers, C W
Published in The American journal of otology (New York, N.Y.) (01.05.1999)
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Published in The American journal of otology (New York, N.Y.) (01.05.1999)
Journal Article
Hearing loss in the Saethre-Chotzen syndrome
Ensink, R J, Marres, H A, Brunner, H G, Cremers, C W
Published in Journal of laryngology and otology (01.10.1996)
Published in Journal of laryngology and otology (01.10.1996)
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Journal Article
Early-Onset Sensorineural Hearing Loss and Late-Onset Neurologic Complaints Caused by a Mitochondrial Mutation at Position 7472
Ensink, Robbert J. H, Verhoeven, Kristien, Marres, Henri A. M, Huygen, Patrick L. M, Padberg, Georges W, ter Laak, Henk, van Camp, Guy, Willems, Patrick J, Cremers, Cor W. R. J
Published in Archives of otolaryngology--head & neck surgery (01.08.1998)
Published in Archives of otolaryngology--head & neck surgery (01.08.1998)
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Journal Article
A highly mobile laryngeal tumour: inspiratory stridor and coughing attacks
De Boer, H. D., Van Diejen, D., Gielen, M. J. M., Ensink, R. J.
Published in Anaesthesia (01.01.2002)
Published in Anaesthesia (01.01.2002)
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Journal Article
A dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13
Ensink, R J H, Huygen, P L M, Snoeckk, R L, Caethoven, G
Published in Clinical otolaryngology (01.08.2001)
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Published in Clinical otolaryngology (01.08.2001)
Journal Article
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene
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
Published in European journal of human genetics : EJHG (01.01.1999)
Published in European journal of human genetics : EJHG (01.01.1999)
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Journal Article
Speech Recognition Scores Related to Age and Degree of Hearing Impairment in DFNA2/KCNQ4 and DFNA9/COCH
Bom, Steven J. H, De Leenheer, Els M. R, Lemaire, François X, Kemperman, Martijn H, Verhagen, Wim I. M, Marres, Henri A. M, Kunst, Henricus P. M, Ensink, Robbert J. H, Bosman, Arjan J, Van Camp, Guy, Cremers, Frans P. M, Huygen, Patrick L. M, Cremers, Cor W. R. J
Published in Archives of otolaryngology--head & neck surgery (01.09.2001)
Published in Archives of otolaryngology--head & neck surgery (01.09.2001)
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Journal Article
A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13
Ensink, R.J.H., Huygen, P.L.M., Snoeckx, R.L., Caethoven, G., Van Camp, G., Cremers, C.W.R.J.
Published in Clinical otolaryngology and allied sciences (01.08.2001)
Published in Clinical otolaryngology and allied sciences (01.08.2001)
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Journal Article