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Results: 1-25 | 26-50 | 51-54
Results: 26-50/54
Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13
Authors: McGuirt, WT Lesperance, MM Wilcox, ER Chen, AH Van Camp, G Smith, RJH
Citation: Wt. Mcguirt et al., Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13, ADV OTO-RH, 56, 2000, pp. 84-96
Maternally inherited hearing impairment
Authors: Van Camp, G Smith, RJH
Citation: G. Van Camp et Rjh. Smith, Maternally inherited hearing impairment, CLIN GENET, 57(6), 2000, pp. 409-414
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
High resolution imaging of the mouse inner ear by microtomography: A new tool in inner ear research
Authors: Van Spaendonck, MP Cryns, K Van de Heyning, PH Scheuermann, DW Van Camp, G Timmermans, JP
Citation: Mp. Van Spaendonck et al., High resolution imaging of the mouse inner ear by microtomography: A new tool in inner ear research, ANAT REC, 259(2), 2000, pp. 229-236
Comparison of transthoracic echocardiography with echocardiography second harmonic imaging with transesophageal echocardiography in the detection of right to left shunts
Authors: Van Camp, G Franken, P Melis, P Cosyns, B Schoors, D Vanoverschelde, JL
Citation: G. Van Camp et al., Comparison of transthoracic echocardiography with echocardiography second harmonic imaging with transesophageal echocardiography in the detection of right to left shunts, AM J CARD, 86(11), 2000, pp. 1284
Twiddler's syndrome
Authors: Hagers, Y Van Camp, G Schoors, D
Citation: Y. Hagers et al., Twiddler's syndrome, ACT CARDIOL, 55(1), 2000, pp. 53-54
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
Determination of the carrier frequency of the common GJB2 (Connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method
Authors: Storm, K Willocx, S Flothmann, K Van Camp, G
Citation: K. Storm et al., Determination of the carrier frequency of the common GJB2 (Connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method, HUM MUTAT, 14(3), 1999, pp. 263-266
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss
Authors: Alloisio, N Morle, L Bozon, M Godet, J Verhoeven, K Van Camp, G Plauchu, H Muller, P Collet, L Lina-Granade, G
Citation: N. Alloisio et al., Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss, EUR J HUM G, 7(2), 1999, pp. 255-258
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
Pulmonary stenosis caused by extrinsic compression of an aortic pseudoaneurysm of a composite aortic graft
Authors: Van Camp, G De Mey, J Daenen, W Budts, W Schoors, D
Citation: G. Van Camp et al., Pulmonary stenosis caused by extrinsic compression of an aortic pseudoaneurysm of a composite aortic graft, J AM S ECHO, 12(11), 1999, pp. 997-1000
Alpha-tectorin involvement in hearing disabilities: one gene two phenotypes
Authors: Balciuniene, J Dahl, N Jalonen, P Verhoeven, K Van Camp, G Borg, E Pettersson, U Jazin, EE
Citation: J. Balciuniene et al., Alpha-tectorin involvement in hearing disabilities: one gene two phenotypes, HUM GENET, 105(3), 1999, pp. 211-216
Non-syndromic hearing loss associated with enlarged vestibular aqueduct iscaused by PDS mutations
Authors: Usami, S Abe, S Weston, MD Shinkawa, H Van Camp, G Kimberling, WJ
Citation: S. Usami et al., Non-syndromic hearing loss associated with enlarged vestibular aqueduct iscaused by PDS mutations, HUM GENET, 104(2), 1999, pp. 188-192
Cloning genes for non-syndromal hearing impairment
Authors: Smith, RJH Van Camp, G
Citation: Rjh. Smith et G. Van Camp, Cloning genes for non-syndromal hearing impairment, BR J AUDIOL, 33(5), 1999, pp. 271-278
The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner ear
Authors: Van Hauwe, P Coucke, P Van Camp, G
Citation: P. Van Hauwe et al., The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner ear, BR J AUDIOL, 33(5), 1999, pp. 285-289
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
Authors: Fransen, E Van Camp, G
Citation: E. Fransen et G. Van Camp, The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?, BR J AUDIOL, 33(5), 1999, pp. 297-302
Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations - molecular and audiological findings
Authors: Mueller, RF Nehammer, A Middleton, A Houseman, M Taylor, GR Bitner-Glindzciz, M Van Camp, G Parker, M Young, ID Davis, A Newton, VE Lench, NJ
Citation: Rf. Mueller et al., Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations - molecular and audiological findings, INT J PED O, 50(1), 1999, pp. 3-13
Non-syndromic hearing impairment: gene linkage and cloning
Authors: Smith, RJH Van Camp, G
Citation: Rjh. Smith et G. Van Camp, Non-syndromic hearing impairment: gene linkage and cloning, INT J PED O, 49, 1999, pp. S159-S163
Cardiac and autonomic evaluation in a pediatric population with human immunodeficiency virus
Authors: Plein, D Van Camp, G Cosyns, B Alimenti, A Levy, J Vandenbossche, JL
Citation: D. Plein et al., Cardiac and autonomic evaluation in a pediatric population with human immunodeficiency virus, CLIN CARD, 22(1), 1999, pp. 33-36
Autosomal recessive nonsyndromic hearing loss
Authors: Sundstrom, RA Van Laer, L Van Camp, G Smith, RJH
Citation: Ra. Sundstrom et al., Autosomal recessive nonsyndromic hearing loss, AM J MED G, 89(3), 1999, pp. 123-129
Autosomal dominant nonsyndromic hearing impairment
Authors: Van Laer, L McGuirt, WT Yang, T Smith, RJH Van Camp, G
Citation: L. Van Laer et al., Autosomal dominant nonsyndromic hearing impairment, AM J MED G, 89(3), 1999, pp. 167-174
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
Risultati: 1-25 | 26-50 | 51-54