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Results: 1-9 |
Results: 9
Hereditary otovestibular dysfunction and Meniere's disease in a large Belgian family is caused by a missense mutation in the COCH gene
Authors: Verstreken, M Declau, F Wuyts, FL D'Haese, P Van Camp, G Fransen, E Van den Hauwe, L Buyle, S Smets, REM Feenstra, L Van der Stappen, A Van de Heyning, PH
Citation: M. Verstreken et al., Hereditary otovestibular dysfunction and Meniere's disease in a large Belgian family is caused by a missense mutation in the COCH gene, OTOL NEURO, 22(6), 2001, pp. 874-881
Prevalence of otosclerosis in an unselected series of temporal bones
Authors: Declau, F Van Spaendonck, M Timmermans, JP Michaels, L Liang, J Qiu, JP Van de Heyning, P
Citation: F. Declau et al., Prevalence of otosclerosis in an unselected series of temporal bones, OTOL NEURO, 22(5), 2001, pp. 596-602
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation
Authors: Fransen, E Verstreken, M Bom, SJH Lemaire, F Kemperman, MH De Kok, YJM Wuyts, FL Verhagen, WIM Huygen, PLM McGuirt, WT Smith, RJH Van Maldergem, L Declau, F Cremers, CWRJ Van de Heyning, PH Cremers, FPM Van Camp, G
Citation: E. Fransen et al., A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation, J MED GENET, 38(1), 2001, pp. 61-64
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36
Authors: Van den Bogaert, K Govaerts, PJ Schatteman, I Brown, MR Caethoven, G Offeciers, FE Somers, T Declau, F Coucke, P Van de Heyning, P Smith, RJH Van Camp, G
Citation: K. Van Den Bogaert et al., A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36, AM J HU GEN, 68(2), 2001, pp. 495-500
Audiometric analysis of a Belgian family linked to the DFNA10 locus
Authors: Verstreken, M Declau, F Schatteman, I Van Velzen, D Verhoeven, K Van Camp, G Willems, PJ Kuhweide, EW Verhaert, E D'Haese, P Wuyts, FL Van de Heyning, PH
Citation: M. Verstreken et al., Audiometric analysis of a Belgian family linked to the DFNA10 locus, AM J OTOL, 21(5), 2000, pp. 675-681
Deafness linked to DFNA2: one locus but how many genes?
Authors: Van Hauwe, P Coucke, PJ Declau, F Kunst, H Ensink, RJ Marres, HA Cremers, CWRJ Djelantik, B Smith, SD Kelley, P Van de Heyning, PH Van Camp, G
Citation: P. Van Hauwe et al., Deafness linked to DFNA2: one locus but how many genes?, NAT GENET, 21(3), 1999, pp. 263-263
High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene
Authors: Fransen, E Verstreken, M Verhagen, WIM Wuyts, FL Huygen, PLM D'Haese, P Robertson, NG Morton, CC McGuirt, WT Smith, RJH Declau, F Van de Heyning, PH Van Camp, G
Citation: E. Fransen et al., High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene, HUM MOL GEN, 8(8), 1999, pp. 1425-1429
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families
Authors: Coucke, PJ Van Hauwe, P Kelley, PM Kunst, H Schatteman, I Van Velzen, D Meyers, J Ensink, RJ Verstreken, M Declau, F Marres, H Kastury, K Bhasin, S McGuirt, WT Smith, RJH Cremers, CWRJ Van de Heyning, P Willems, PJ Smith, SD Van Camp, G
Citation: Pj. Coucke et al., Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families, HUM MOL GEN, 8(7), 1999, pp. 1321-1328
Diagnosis and management strategies in congenital atresia of the external auditory canal
Authors: Declau, F Cremers, C Van de Heyning, P Amadori, M Casselman, J Causse, JB Charachon, R Granstrom, G Martini, A Offeciers, E Somers, T Tos, M
Citation: F. Declau et al., Diagnosis and management strategies in congenital atresia of the external auditory canal, BR J AUDIOL, 33(5), 1999, pp. 313-327
Risultati: 1-9 |