Verhoeven K - Search Results

1

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. Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60. Nat Genet. 1998. PMID: 9590290

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. Am J Hum Genet. 1997 May;60(5):1168-73. Am J Hum Genet. 1997. PMID: 9150164 Free PMC article.

3

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.

Verhoeven K, Ensink RJ, Tiranti V, Huygen PL, Johnson DF, Schatteman I, Van Laer L, Verstreken M, Van de Heyning P, Fischel-Ghodsian N, Zeviani M, Cremers CW, Willems PJ, Van Camp G. Verhoeven K, et al. Eur J Hum Genet. 1999 Jan;7(1):45-51. doi: 10.1038/sj.ejhg.5200247. Eur J Hum Genet. 1999. PMID: 10094190

4

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.

Verhoeven K, Fagerheim T, Prasad S, Wayne S, De Clau F, Balemans W, Verstreken M, Schatteman I, Solem B, Van de Heyning P, Tranebjärg L, Smith RJ, Van Camp G. Verhoeven K, et al. Hum Genet. 2000 Jul;107(1):7-11. doi: 10.1007/s004390000319. Hum Genet. 2000. PMID: 10982027

5

Clinical presentation of DFNA8-DFNA12.

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: verhoeven k. Adv Otorhinolaryngol. 2002;61:60-5. doi: 10.1159/000066805. Adv Otorhinolaryngol. 2002. PMID: 12408064 No abstract available.

6

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: verhoeven k. Am J Otol. 1998 Nov;19(6):718-23. Am J Otol. 1998. PMID: 9831143

7

Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

Alloisio N, Morlé L, Bozon M, Godet J, Verhoeven K, Van Camp G, Plauchu H, Muller P, Collet L, Lina-Granade G. Alloisio N, et al. Among authors: verhoeven k. Eur J Hum Genet. 1999 Feb-Mar;7(2):255-8. doi: 10.1038/sj.ejhg.5200273. Eur J Hum Genet. 1999. PMID: 10196713

8

DFNA 2, 5, 8, 12.

Van Camp G, Coucke PJ, Van Hauwe P, Van Laer L, Verhoeven K, Wuyts F, Smith RJ. Van Camp G, et al. Among authors: verhoeven k. Adv Otorhinolaryngol. 2000;56:68-77. doi: 10.1159/000059084. Adv Otorhinolaryngol. 2000. PMID: 10868216 Review. No abstract available.

9

Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes.

Balciuniene J, Dahl N, Jalonen P, Verhoeven K, Van Camp G, Borg E, Pettersson U, Jazin EE. Balciuniene J, et al. Among authors: verhoeven k. Hum Genet. 1999 Sep;105(3):211-6. doi: 10.1007/s004390051091. Hum Genet. 1999. PMID: 10987647

10

A deafness mutation isolates a second role for the tectorial membrane in hearing.

Legan PK, Lukashkina VA, Goodyear RJ, Lukashkin AN, Verhoeven K, Van Camp G, Russell IJ, Richardson GP. Legan PK, et al. Among authors: verhoeven k. Nat Neurosci. 2005 Aug;8(8):1035-42. doi: 10.1038/nn1496. Epub 2005 Jul 3. Nat Neurosci. 2005. PMID: 15995703

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