Features of autosomal recessive non-syndromic hearing impairment: a review to serve as a reference
Oonk, A.M.M., Huygen, P.L.M., Kunst, H.P.M., Kremer, H., Pennings, R.J.E.
Published in Clinical otolaryngology (01.10.2016)
Published in Clinical otolaryngology (01.10.2016)
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Journal Article
Ear and hearing problems in relation to karyotype in children with Turner syndrome
Verver, E.J.J., Freriks, K., Thomeer, H.G.X.M., Huygen, P.L.M., Pennings, R.J.E., Alfen-van der Velden, A.A.E.M., Timmers, H.J., Otten, B.J., Cremers, C.W.R.J., Kunst, H.P.M.
Published in Hearing research (01.05.2011)
Published in Hearing research (01.05.2011)
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Journal Article
Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family
Weegerink, N.J.D., Huygen, P.L.M., Schraders, M., Kremer, H., Pennings, R.J.E., Kunst, H.P.M.
Published in Hearing research (01.12.2011)
Published in Hearing research (01.12.2011)
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Journal Article
Usefulness of additional measurements of the median nerve with ultrasonography
Claes, F., Meulstee, J., Claessen-Oude Luttikhuis, T. T. M., Huygen, P. L. M., Verhagen, W. I. M.
Published in Neurological sciences (01.12.2010)
Published in Neurological sciences (01.12.2010)
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Journal Article
Audiometric characteristics of a Dutch family with Muckle-Wells syndrome
Weegerink, N.J.D., Schraders, M., Leijendeckers, J., Slieker, K., Huygen, P.L.M., Hoefsloot, L., Oostrik, J., Pennings, R.J.E., Simon, A., Snik, A., Kremer, H., Kunst, H.P.M.
Published in Hearing research (01.12.2011)
Published in Hearing research (01.12.2011)
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Journal Article
Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis
Oonk, A.M.M., Leijendeckers, J.M., Lammers, E.M., Weegerink, N.J.D., Oostrik, J., Beynon, A.J., Huygen, P.L.M., Kunst, H.P.M., Kremer, H., Snik, A.F.M., Pennings, R.J.E.
Published in Hearing research (01.05.2013)
Published in Hearing research (01.05.2013)
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Journal Article
A genotype-phenotype correlation for GJB2 (connexin 26) deafness
Cryns, K, Orzan, E, Murgia, A, Huygen, P L M, Moreno, F, del Castillo, I, Parker Chamberlin, G, Azaiez, H, Prasad, S, Cucci, R A, Leonardi, E, Snoeckx, R L, Govaerts, P J, Van de Heyning, P H, Van de Heyning, C M, Smith, R J H, Van Camp, G
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
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Journal Article
Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2)
van Beelen, E., Leijendeckers, J.M., Huygen, P.L.M., Admiraal, R.J.C., Hoefsloot, L.H., Lichtenbelt, K.D., Stöbe, L., Pennings, R.J.E., Leuwer, R., Snik, A.F.M., Kunst, H.P.M.
Published in Hearing research (01.09.2012)
Published in Hearing research (01.09.2012)
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Journal Article
Audiometric Characteristics of a Dutch Family with a New Mutation in GATA3 Causing HDR Syndrome
van Beelen, E., Leijendeckers, J.M., Admiraal, R.J.C., Huygen, P.L.M., Hoefsloot, L.H., Pennings, R.J.E., Snik, A.F.M., Kunst, H.P.M.
Published in Audiology & neurotology (01.01.2014)
Published in Audiology & neurotology (01.01.2014)
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Journal Article
A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44
Schrauwen, I, Weegerink, NJD, Fransen, E, Claes, C, Pennings, RJE, Cremers, CWRJ, Huygen, PLM, Kunst, HPM, Van Camp, G
Published in Clinical genetics (01.05.2011)
Published in Clinical genetics (01.05.2011)
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Journal Article
Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3
van Beelen, E., Schraders, M., Huygen, P.L.M., Oostrik, J., Plantinga, R.F., van Drunen, W., Collin, R.W.J., Kooper, D.P., Pennings, R.J.E., Cremers, C.W.R.J., Kremer, H., Kunst, H.P.M.
Published in Hearing research (01.06.2013)
Published in Hearing research (01.06.2013)
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Journal Article
High Prevalence of Symptoms of Menière's Disease in three Families With a Mutation in the COCH Gene
Fransen, Erik, Verstreken, Margriet, Verhagen, Wim I. M., Wuyts, Floris L., Huygen, Patrick L.M., D'Haese, Patrick, Robertson, Nahid G., Morton, Cynthia C., McGuirt, Wyman T., Smith, Richard J. H., Declau, Frank, Van de Heyning, Paul H., Van Camp, Guy
Published in Human molecular genetics (01.08.1999)
Published in Human molecular genetics (01.08.1999)
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Journal Article
Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA : Some Evidence for Protection of the Inner Ear
DE HEER, A. R, PAUW, R. J, HUYGEN, P. L. M, COLLIN, R. W. J, KREMER, H, CREMERS, C. W. R. J
Published in Audiology & neurotology (2009)
Published in Audiology & neurotology (2009)
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Journal Article
Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of Genotypes
Bom, S. J. H., Kunst, H. P. M., Huygen, P. L. M., Cremers, F. P. M., Cremers, C.W. RJ
Published in British Journal of Audiology (01.10.1999)
Published in British Journal of Audiology (01.10.1999)
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Journal Article
Conference Proceeding
Sensorineural hearing impairment in patients with Pmp22 duplication, deletion, and frameshift mutations
Verhagen, W I M, Huygen, P L M, Gabreëls-Festen, A A W M, Engelhart, M, van Mierlo, P J W B, van Engelen, B G M
Published in Otology & neurotology (01.05.2005)
Published in Otology & neurotology (01.05.2005)
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Journal Article
Familial aggregation of tinnitus: a European multicentre study
Hendrickx, J J, Huyghe, J R, Demeester, K, Topsakal, V, Van Eyken, E, Fransen, E, Mäki-Torkko, E, Hannula, S, Jensen, M, Tropitzsch, A, Bonaconsa, A, Mazzoli, M, Espeso, A, Verbruggen, K, Huyghe, J, Huygen, P L M, Kremer, H, Kunst, S J, Manninen, M, Diaz-Lacava, A N, Steffens, M, Parving, A, Pyykkö, I, Dhooge, I, Stephens, D, Orzan, E, Pfister, M H F, Bille, M, Sorri, M, Cremers, C W R J, Van Laer, L, Van Camp, G, Wienker, T F, Van de Heyning, P
Published in B-ENT (Leuven) (2007)
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Published in B-ENT (Leuven) (2007)
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