AAAAAA

   
Results: 1-25 | 26-37 |
Results: 26-37/37
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness
Authors: Karet, FE Finberg, KE Nelson, RD Nayir, A Mocan, H Sanjad, SA Rodriguez-Soriano, J Santos, F Cremers, CWRJ Di Pietro, A Hoffbrand, BI Winiarski, J Bakkaloglu, A Ozen, S Dusunsel, R Goodyer, P Hulton, SA Wu, DK Skvorak, AB Morton, CC Cunningham, MJ Jha, V Lifton, RP
Citation: Fe. Karet et al., Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness, NAT GENET, 21(1), 1999, pp. 84-90
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
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 Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
Authors: de Kok, YJM Bom, SJH Brunt, TM Kemperman, MH van Beusekom, E van der Velde-Visser, SD Robertson, NG Morton, CC Huygen, PLM Verhagen, WIM Brunner, HG Cremers, CWRJ Cremers, FPM
Citation: Yjm. De Kok et al., A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects, HUM MOL GEN, 8(2), 1999, pp. 361-366
The BAHA HC200/300 in comparison with conventional bone conduction hearingaids
Authors: van der Pouw, CTM Snik, AFM Cremers, CWRJ
Citation: Ctm. Van Der Pouw et al., The BAHA HC200/300 in comparison with conventional bone conduction hearingaids, CLIN OTOLAR, 24(3), 1999, pp. 171-176
Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes
Authors: Bom, SJH Kunst, HPM Huygen, PLM Cremers, FPM Cremers, CWRJ
Citation: Sjh. Bom et al., Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes, BR J AUDIOL, 33(5), 1999, pp. 335-348
Proximal symphalangism and congenital conductive hearing loss: Otologic aspects
Authors: Ensink, RJH Sleeckx, JP Cremers, CWRJ
Citation: Rjh. Ensink et al., Proximal symphalangism and congenital conductive hearing loss: Otologic aspects, AM J OTOL, 20(3), 1999, pp. 344-349
Genetic heterogeneity associated with branchio-oto-renal syndrome
Authors: Kumar, S Kimberling, WJ Marres, HAM Cremers, CWRJ
Citation: S. Kumar et al., Genetic heterogeneity associated with branchio-oto-renal syndrome, AM J MED G, 83(3), 1999, pp. 207-208
Progressive cochleovestibular impairment caused by a point mutation in theCOCH gene at DFNA9
Authors: Bom, SJH Kemperman, MH De Kok, YJM Huygen, PLM Verhagen, WIM Cremers, FPM Cremers, CWRJ
Citation: Sjh. Bom et al., Progressive cochleovestibular impairment caused by a point mutation in theCOCH gene at DFNA9, LARYNGOSCOP, 109(9), 1999, pp. 1525-1530
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
First audiometric results with the Vibrant (R) soundbridge, a semi-implantable hearing device for sensorineural hearing loss
Authors: Snik, AFM Cremers, CWRJ
Citation: Afm. Snik et Cwrj. Cremers, First audiometric results with the Vibrant (R) soundbridge, a semi-implantable hearing device for sensorineural hearing loss, AUDIOLOGY, 38(6), 1999, pp. 335-338
Percutaneous implants in the temporal bone for securing a bone conductor: Surgical methods and results
Authors: van der Pouw, CTM Mylanus, EAM Cremers, CWRJ
Citation: Ctm. Van Der Pouw et al., Percutaneous implants in the temporal bone for securing a bone conductor: Surgical methods and results, ANN OTOL RH, 108(6), 1999, pp. 532-536
Risultati: 1-25 | 26-37 |