Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia
Mortier, J., van den Ende, J., Declau, F., Vercruysse, H., Wuyts, W., Van Camp, G., Vanderveken, O., Boudewyns, An
Published in European archives of oto-rhino-laryngology (01.02.2023)
Published in European archives of oto-rhino-laryngology (01.02.2023)
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Prekallikrein deficiency in a 15-year-old boy with Ménière's disease: a case report
Criel, M, Declau, F, Schuermans, C, Ver Elst, K, Vermeiren, S, Weekx, S, Lemmens, J
Published in Acta clinica belgica (English ed. Online) (01.08.2017)
Published in Acta clinica belgica (English ed. Online) (01.08.2017)
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Journal Article
Prevalence of otosclerosis in an unselected series of temporal bones
Declau, F, Van Spaendonck, M, Timmermans, J P, Michaels, L, Liang, J, Qiu, J P, Van de Heyning, P
Published in Otology & neurotology (01.09.2001)
Published in Otology & neurotology (01.09.2001)
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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
Otosclerosis: a genetically heterogeneous disease involving at least three different genes
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
Published in Bone (New York, N.Y.) (01.04.2002)
Published in Bone (New York, N.Y.) (01.04.2002)
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Journal Article
Case report: “Auditory neuropathy” in a newborn caused by a cerebellopontine angle arachnoid cyst
Boudewyns, A.N, Declau, F, De Ridder, D, Parizel, P.M, van den Ende, J, Van de Heyning, P.H
Published in International journal of pediatric otorhinolaryngology (01.06.2008)
Published in International journal of pediatric otorhinolaryngology (01.06.2008)
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Journal Article
Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene
Verstreken, M, Declau, F, Wuyts, F L, D'Haese, P, Van Camp, G, Fransen, E, Van den Hauwe, L, Buyle, S, Smets, R E, Feenstra, L, Van der Stappen, A, Van de Heyning, P H
Published in Otology & neurotology (01.11.2001)
Published in Otology & neurotology (01.11.2001)
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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 New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene
Van Camp, Guy, Snoeckx, Rikkert L., Hilgert, Nele, van den Ende, Jenneke, Fukuoka, Hisakumi, Wagatsuma, Michio, Suzuki, Hiroaki, Erica Smets, R.M., Vanhoenacker, Filip, Declau, Frank, Van De Heyning, Paul, Usami, Shin-ichi
Published in American journal of human genetics (01.09.2006)
Published in American journal of human genetics (01.09.2006)
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Journal Article
Audiometric analysis of a Belgian family linked to the DFNA10 locus
Verstreken, M, Declau, F, Schatteman, I, Van Velzen, D, Verhoeven, K, Van Camp, G, Willems, P J, Kuhweide, E W, Verhaert, E, D'Haese, P, Wuyts, F L, Van de Heyning, P H
Published in The American journal of otology (New York, N.Y.) (01.09.2000)
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Published in The American journal of otology (New York, N.Y.) (01.09.2000)
Journal Article
Association of Bone Morphogenetic Proteins With Otosclerosis
Schrauwen, Isabelle, Thys, Melissa, Vanderstraeten, Kathleen, Fransen, Erik, Dieltjens, Nele, Huyghe, Jeroen R, Ealy, Megan, Claustres, Mireille, Cremers, Cor RWJ, Dhooge, Ingeborg, Declau, Frank, Van de Heyning, Paul, Vincent, Robert, Somers, Thomas, Offeciers, Erwin, Smith, Richard JH, Van Camp, Guy
Published in Journal of bone and mineral research (01.04.2008)
Published in Journal of bone and mineral research (01.04.2008)
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Journal Article
Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)
Donaudy, Francesca, Snoeckx, Rik, Pfister, Markus, Zenner, Hans-Peter, Blin, Nikolaus, Di Stazio, Mariateresa, Ferrara, Antonella, Lanzara, Carmen, Ficarella, Romina, Declau, Frank, Pusch, Carsten M., Nürnberg, Peter, Melchionda, Salvatore, Zelante, Leopoldo, Ballana, Ester, Estivill, Xavier, Van Camp, Guy, Gasparini, Paolo, Savoia, Anna
Published in American journal of human genetics (01.04.2004)
Published in American journal of human genetics (01.04.2004)
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Journal Article
22q11.2 microduplication syndrome with congenital aural atresia: a family report
Boudewyns, An, van den Ende, Jenneke, Boiy, Tine, Van de Heyning, Paul, Declau, Frank
Published in Otology & neurotology (01.06.2012)
Published in Otology & neurotology (01.06.2012)
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