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Results: 1-25 | 26-37
Results: 1-25/37
Clinical experience with the vibrant soundbridge implant device
Authors: Fisch, U Cremers, CWRJ Lenarz, T Weber, B Babighian, G Uziel, AS Proops, DW O'Connor, AF Charachon, R Helms, J Fraysse, B
Citation: U. Fisch et al., Clinical experience with the vibrant soundbridge implant device, OTOL NEURO, 22(6), 2001, pp. 962-972
Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome
Authors: Kemperman, MH Stinckens, C Kumar, S Huygen, PLM Joosten, FBM Cremers, CWRJ
Citation: Mh. Kemperman et al., Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome, OTOL NEURO, 22(5), 2001, pp. 637-643
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
Authors: Bespalova, IN Van Camp, G Bom, SJH Brown, DJ Cryns, K DeWan, AT Erson, AE Flothmann, K Kunst, HPM Kurnool, P Sivakumaran, TA Cremers, CWRJ Leal, SM Burmeister, M Lesperance, MM
Citation: In. Bespalova et al., Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss, HUM MOL GEN, 10(22), 2001, pp. 2501-2508
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH
Authors: Bom, SJH De Leenheer, EMR Lemaire, FX Kemperman, MH Verhagen, WIM Marres, HAM Kunst, HPM Ensink, RJH Bosman, AJ Van Camp, G Cremers, FPM Huygen, PLM Cremers, CWRJ
Citation: Sjh. Bom et al., Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH, ARCH OTOLAR, 127(9), 2001, pp. 1045-1048
A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13
Authors: Ensink, RJH Huygen, PLM Snoeckx, RL Caethoven, G Van Camp, G Cremers, CWRJ
Citation: Rjh. Ensink et al., A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13, CLIN OTOLAR, 26(4), 2001, pp. 310-316
Fluctuant, progressive hearing loss associated with Meniere like vertigo in three patients with the Pendred syndrome
Authors: Stinckens, C Huygen, PLM Joosten, FBM Van Camp, G Otten, B Cremers, CWRJ
Citation: C. Stinckens et al., Fluctuant, progressive hearing loss associated with Meniere like vertigo in three patients with the Pendred syndrome, INT J PED O, 61(3), 2001, pp. 207-215
The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the Branchio-Oto-Renal syndrome. A family study
Authors: Stinckens, C Standaert, L Casselman, JW Huygen, PLM Kumar, S Van de Wallen, J Cremers, CWRJ
Citation: C. Stinckens et al., The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the Branchio-Oto-Renal syndrome. A family study, INT J PED O, 59(3), 2001, pp. 163-172
The bone-anchored hearing aid - A solution for previously unresolved otologic problems
Authors: Snik, AFM Mylanus, EAM Cremers, CWRJ
Citation: Afm. Snik et al., The bone-anchored hearing aid - A solution for previously unresolved otologic problems, OTOLAR CLIN, 34(2), 2001, pp. 365
Multicenter audiometric results with the Vibrant Soundbridge, a semi-implantable hearing device for sensorineural hearing impairment
Authors: Snik, AFM Mylanus, EAM Cremers, CWRJ Dillier, N Fisch, U Gnadeberg, D Lenarz, T Mazolli, M Babighian, G Uziel, AS Cooper, HR O'Connor, AF Fraysse, B Charachon, R Shehata-Dieler, WE
Citation: Afm. Snik et al., Multicenter audiometric results with the Vibrant Soundbridge, a semi-implantable hearing device for sensorineural hearing impairment, OTOLAR CLIN, 34(2), 2001, pp. 373
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
Audiometric evaluation of bilaterally fined bone-anchored hearing aids
Authors: Bosman, AJ Snik, AFM van der Pouw, CTM Mylanus, EAM Cremers, CWRJ
Citation: Aj. Bosman et al., Audiometric evaluation of bilaterally fined bone-anchored hearing aids, AUDIOLOGY, 40(3), 2001, pp. 158-167
A common ancestral origin of the frequent and widespread 2299delG USH2A mutation (vol 69, pg 228, 2001)
Authors: Dreyer, B Tranebjaerg, L Brox, V Rosenberg, T Moller, C Beneyto, M Weston, MD Kimberling, WJ Cremers, CWRJ Liu, XZ Nilssen, O
Citation: B. Dreyer et al., A common ancestral origin of the frequent and widespread 2299delG USH2A mutation (vol 69, pg 228, 2001), AM J HU GEN, 69(4), 2001, pp. 922-922
Developmental aspects of the rat endolymphatic sac and functional implications
Authors: Peters, TA Tonnaer, ELGM Kuijpers, W Cremers, CWRJ Curfs, JHAJ
Citation: Ta. Peters et al., Developmental aspects of the rat endolymphatic sac and functional implications, ACT OTO-LAR, 121(2), 2001, pp. 125-129
A Dutch family with progressive sensorineural hearing impairment linked tothe DFNA2 region
Authors: Ensink, RJH Huygen, PLM Van Hauwe, P Coucke, P Cremers, CWRJ Van Camp, G
Citation: Rjh. Ensink et al., A Dutch family with progressive sensorineural hearing impairment linked tothe DFNA2 region, EUR ARCH OT, 257(2), 2000, pp. 62-67
The effect of the "floating mass transducer" in the middle ear on hearing sensitivity
Authors: Snik, AFM Cremers, CWRJ
Citation: Afm. Snik et Cwrj. Cremers, The effect of the "floating mass transducer" in the middle ear on hearing sensitivity, AM J OTOL, 21(1), 2000, pp. 42-48
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominanthearing loss, cluster in the channel pore region
Authors: Van Hauwe, P Coucke, PJ Ensink, RJ Huygen, P Cremers, CWRJ Van Camp, G
Citation: P. Van Hauwe et al., Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominanthearing loss, cluster in the channel pore region, AM J MED G, 93(3), 2000, pp. 184-187
The ins and outs of X-linked deafness type 3
Authors: Cremers, FPM Cremers, CWRJ Ropers, HH
Citation: Fpm. Cremers et al., The ins and outs of X-linked deafness type 3, ADV OTO-RH, 56, 2000, pp. 184-195
Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation
Authors: Admiraal, RJC Brunner, HG Dijkstra, TL Huygen, PLM Cremers, CWRJ
Citation: Rjc. Admiraal et al., Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation, LARYNGOSCOP, 110(3), 2000, pp. 457-461
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q
Authors: Pieke-Dahl, S Moller, CG Kelley, PM Astuto, LM Cremers, CWRJ Gorin, MB Kimberling, WJ
Citation: S. Pieke-dahl et al., Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q, J MED GENET, 37(4), 2000, pp. 256-262
Hearing: cracking the code
Authors: Cremers, CWRJ
Citation: Cwrj. Cremers, Hearing: cracking the code, J LARYNG OT, 114(1), 2000, pp. 6-16
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)
Authors: Verhagen, WIM Bom, SJH Huygen, PLM Fransen, E Van Camp, G Cremers, CWRJ
Citation: Wim. Verhagen et al., Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9), ARCH NEUROL, 57(7), 2000, pp. 1045-1047
Genetic heterogeneity of Usher syndrome: Analysis of 151 families with Usher type I
Authors: Astuto, LM Weston, MD Carney, CA Hoover, DM Cremers, CWRJ Wagenaar, M Moller, C Smith, RJH Pieke-Dahl, S Greenberg, J Ramesar, R Jacobson, SG Ayuso, C Heckenlively, JR Tamayo, M Gorin, MB Reardon, W Kimerling, WJ
Citation: Lm. Astuto et al., Genetic heterogeneity of Usher syndrome: Analysis of 151 families with Usher type I, AM J HU GEN, 67(6), 2000, pp. 1569-1574
Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: Clinical and genetic implications
Authors: Kumar, S Deffenbacher, K Marres, HAM Cremers, CWRJ Kimberling, WJ
Citation: S. Kumar et al., Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: Clinical and genetic implications, AM J HU GEN, 66(5), 2000, pp. 1715-1720
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
Authors: McGuirt, WT Prasad, SD Griffith, AJ Kunst, HPM Green, GE Shpargel, KB Runge, C Huybrechts, C Mueller, RF Lynch, E King, MC Brunner, HG Cremers, CWRJ Takanosu, M Li, SW Arita, M Mayne, R Prockop, DJ Van Camp, G Smith, RJH
Citation: Wt. Mcguirt et al., Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13), NAT GENET, 23(4), 1999, pp. 413-419
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
Risultati: 1-25 | 26-37