Verhoeven K - Search Results

1

Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472.

Ensink RJ, Verhoeven K, Marres HA, Huygen PL, Padberg GW, ter Laak H, van Camp G, Willems PJ, Cremers CW. Ensink RJ, et al. Among authors: verhoeven k. Arch Otolaryngol Head Neck Surg. 1998 Aug;124(8):886-91. doi: 10.1001/archotol.124.8.886. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9708714

2

Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.

Chen AH, Mueller RF, Prasad SD, Greinwald JH Jr, Manaligod J, Muilenburg AC, Verhoeven K, Van Camp G, Smith RJ. Chen AH, et al. Among authors: verhoeven k. Arch Otolaryngol Head Neck Surg. 1998 Jan;124(1):20-4. doi: 10.1001/archotol.124.1.20. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9440775 Review.

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

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: verhoeven k. Am J Otol. 2000 Sep;21(5):675-81. Am J Otol. 2000. PMID: 10993457

5

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

6

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.

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

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.

9

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.

Wayne S, Robertson NG, DeClau F, Chen N, Verhoeven K, Prasad S, Tranebjärg L, Morton CC, Ryan AF, Van Camp G, Smith RJ. Wayne S, et al. Among authors: verhoeven k. Hum Mol Genet. 2001 Feb 1;10(3):195-200. doi: 10.1093/hmg/10.3.195. Hum Mol Genet. 2001. PMID: 11159937

10

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

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