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Results: 1-11 |
Results: 11
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
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
Depletion of circulating alpha(2)-antiplasmin by intravenous plasmin or immunoneutralization reduces focal cerebral ischemic injury in the absence ofarterial recanalization
Authors: Nagai, N De Mol, M Van Hoef, B Verstreken, M Collen, D
Citation: N. Nagai et al., Depletion of circulating alpha(2)-antiplasmin by intravenous plasmin or immunoneutralization reduces focal cerebral ischemic injury in the absence ofarterial recanalization, BLOOD, 97(10), 2001, pp. 3086-3092
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment
Authors: Verhoeven, K Fagerheim, T Prasad, S Wayne, S De Clau, F Balemans, W Verstreken, M Schatteman, I Solem, B Van de Heyning, P Tranebjarg, L Smith, RJH Van Camp, G
Citation: K. Verhoeven et al., Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment, HUM GENET, 107(1), 2000, pp. 7-11
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
Accelerated neointima formation after vascular injury in mice with stromelysin-3 (MMP-11) gene inactivation
Authors: Lijnen, HR Van Hoef, B Vanlinthout, I Verstreken, M Rio, MC Collen, D
Citation: Hr. Lijnen et al., Accelerated neointima formation after vascular injury in mice with stromelysin-3 (MMP-11) gene inactivation, ART THROM V, 19(12), 1999, pp. 2863-2870
Hearing impairment and neurological dysfunction associated with a mutationin the mitochondrial tRNA(Ser(UCN)) gene
Authors: Verhoeven, K Ensink, RJH Tiranti, V Huygen, PLM Johnson, DF Schatteman, I Van Laer, L Verstreken, M Van de Heyning, P Fischel-Ghodsian, N Zeviani, M Cremers, CWRJ Willems, PJ Van Camp, G
Citation: K. Verhoeven et al., Hearing impairment and neurological dysfunction associated with a mutationin the mitochondrial tRNA(Ser(UCN)) gene, EUR J HUM G, 7(1), 1999, pp. 45-51
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
A gene for autosomal dominant hearing impairment (DFNA14) maps to a regionon chromosome 4p16.3 that does not overlap the DFNA6 locus
Authors: Van Camp, G Kunst, H Flothmann, K McGuirt, W Wauters, J Marres, H Verstreken, M Bespalova, IN Burmeister, M Van de Heyning, PH Smith, RJH Willems, PJ Cremers, CWRJ Lesperance, MM
Citation: G. Van Camp et al., A gene for autosomal dominant hearing impairment (DFNA14) maps to a regionon chromosome 4p16.3 that does not overlap the DFNA6 locus, J MED GENET, 36(7), 1999, pp. 532-536
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic,midfrequency, prelingual and nonprogressive sensorineural hearing loss
Authors: Govaerts, PJ De Ceulaer, G Daemers, K Verhoeven, K Van Camp, G Schatteman, I Verstreken, M Willems, PJ Somers, T Offeciers, FE
Citation: Pj. Govaerts et al., A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic,midfrequency, prelingual and nonprogressive sensorineural hearing loss, AM J OTOL, 19(6), 1998, pp. 718-723
Risultati: 1-11 |