Kunst HP - Search Results

1

Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.

Weegerink NJ, Huygen PL, Schraders M, Kremer H, Pennings RJ, Kunst HP. Weegerink NJ, et al. Among authors: kunst hp. Hear Res. 2011 Dec;282(1-2):167-77. doi: 10.1016/j.heares.2011.08.010. Epub 2011 Aug 27. Hear Res. 2011. PMID: 21893181

2

Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2.

Marres H, van Ewijk M, Huygen P, Kunst H, van Camp G, Coucke P, Willems P, Cremers C. Marres H, et al. Arch Otolaryngol Head Neck Surg. 1997 Jun;123(6):573-7. doi: 10.1001/archotol.1997.01900060015002. Arch Otolaryngol Head Neck Surg. 1997. PMID: 9193215 Free article.

3

Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2.

Kunst H, Marres H, Huygen P, Ensink R, Van Camp G, Van Hauwe P, Coucke P, Willems P, Cremers C. Kunst H, et al. Laryngoscope. 1998 Jan;108(1 Pt 1):74-80. doi: 10.1097/00005537-199801000-00014. Laryngoscope. 1998. PMID: 9432071

4

Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.

Kunst H, Marres H, Huygen P, Van Camp G, Joosten F, Cremers C. Kunst H, et al. Audiology. 1999 May-Jun;38(3):165-73. doi: 10.3109/00206099909073018. Audiology. 1999. PMID: 10437687 Review.

5

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. Am J Otol. 2000 Mar;21(2):181-7. doi: 10.1016/s0196-0709(00)80006-x. Am J Otol. 2000. PMID: 10733181

6

Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21).

Kunst H, Marres H, Huygen P, van Duijnhoven G, Krebsova A, van der Velde S, Reis A, Cremers F, Cremers C. Kunst H, et al. Clin Otolaryngol Allied Sci. 2000 Feb;25(1):45-54. doi: 10.1046/j.1365-2273.2000.00327.x. Clin Otolaryngol Allied Sci. 2000. PMID: 10764236

7

Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.

Bom SJ, Kunst HP, Huygen PL, Cremers FP, Cremers CW. Bom SJ, et al. Among authors: kunst hp. Br J Audiol. 1999 Oct;33(5):335-48. doi: 10.3109/03005369909090117. Br J Audiol. 1999. PMID: 10890148

8

Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH.

Bom SJ, De Leenheer EM, Lemaire FX, Kemperman MH, Verhagen WI, Marres HA, Kunst HP, Ensink RJ, Bosman AJ, Van Camp G, Cremers FP, Huygen PL, Cremers CW. Bom SJ, et al. Among authors: kunst hp. Arch Otolaryngol Head Neck Surg. 2001 Sep;127(9):1045-8. doi: 10.1001/archotol.127.9.1045. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11556850

9

DFNA2/KCNQ4 and its manifestations.

De Leenheer EM, Ensink RJ, Kunst HP, Marres HA, Talebizadeh Z, Declau F, Smith SD, Usami S, Van de Heyning PH, Van Camp G, Huygen PL, Cremers CW. De Leenheer EM, et al. Among authors: kunst hp. Adv Otorhinolaryngol. 2002;61:41-6. doi: 10.1159/000066802. Adv Otorhinolaryngol. 2002. PMID: 12408061 No abstract available.

10

The phenotype of DFNA13/COL11A2.

De Leenheer EM, McGuirt WT, Kunst HP, Huygen PL, Smith RJ, Cremers CW. De Leenheer EM, et al. Among authors: kunst hp. Adv Otorhinolaryngol. 2002;61:85-91. doi: 10.1159/000066804. Adv Otorhinolaryngol. 2002. PMID: 12408068 No abstract available.

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