Van Camp G - Search Results

1

Focal sclerosis of semicircular canals with severe DFNA9 hearing impairment caused by a P51S COCH-mutation: is there a link?

de Varebeke SP, Termote B, Van Camp G, Govaerts PJ, Schepers S, Cox T, Deben K, Ketelslagers K, Souverijns G. de Varebeke SP, et al. Among authors: van camp g. Otol Neurotol. 2014 Jul;35(6):1077-86. doi: 10.1097/MAO.0000000000000283. Otol Neurotol. 2014. PMID: 24662630

2

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ. Verhoeven K, et al. Among authors: van de heyning ph, van laer l, van camp g. Am J Hum Genet. 1997 May;60(5):1168-73. Am J Hum Genet. 1997. PMID: 9150164 Free PMC article.

3

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G. Verhoeven K, et al. Among authors: van laer l, van de heyning p, van hauwe p, van camp g. Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60. Nat Genet. 1998. PMID: 9590290

4

A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.

Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE. Govaerts PJ, et al. Among authors: van camp g. Am J Otol. 1998 Nov;19(6):718-23. Am J Otol. 1998. PMID: 9831143

5

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

Fransen E, Verstreken M, Verhagen WI, Wuyts FL, Huygen PL, D'Haese P, Robertson NG, Morton CC, McGuirt WT, Smith RJ, Declau F, Van de Heyning PH, Van Camp G. Fransen E, et al. Among authors: van de heyning ph, van camp g. Hum Mol Genet. 1999 Aug;8(8):1425-9. doi: 10.1093/hmg/8.8.1425. Hum Mol Genet. 1999. PMID: 10400989

6

The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.

Kunst H, Huybrechts C, Marres H, Huygen P, Van Camp G, Cremers C. Kunst H, et al. Among authors: van camp g. Am J Otol. 2000 Mar;21(2):181-7. doi: 10.1016/s0196-0709(00)80006-x. Am J Otol. 2000. PMID: 10733181

7

The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?

Fransen E, Van Camp G. Fransen E, et al. Among authors: van camp g. Br J Audiol. 1999 Oct;33(5):297-302. doi: 10.3109/03005369909090113. Br J Audiol. 1999. PMID: 10890144

8

Audiometric analysis of a Belgian family linked to the DFNA10 locus.

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. Verstreken M, et al. Among authors: van de heyning ph, van velzen d, van camp g. Am J Otol. 2000 Sep;21(5):675-81. Am J Otol. 2000. PMID: 10993457

9

A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36.

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 RJ, Van Camp G. Van Den Bogaert K, et al. Among authors: van de heyning p, van camp g. Am J Hum Genet. 2001 Feb;68(2):495-500. doi: 10.1086/318185. Epub 2001 Jan 16. Am J Hum Genet. 2001. PMID: 11170898 Free PMC article.

10

Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene.

Verstreken M, Declau F, Wuyts FL, D'Haese P, Van Camp G, Fransen E, Van den Hauwe L, Buyle S, Smets RE, Feenstra L, Van der Stappen A, Van de Heyning PH. Verstreken M, et al. Among authors: van de heyning ph, van der stappen a, van den hauwe l, van camp g. Otol Neurotol. 2001 Nov;22(6):874-81. doi: 10.1097/00129492-200111000-00028. Otol Neurotol. 2001. PMID: 11698812

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