Kunst HP - Search Results

1

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.

Verver EJ, Topsakal V, Kunst HP, Huygen PL, Heller PG, Pujol-Moix N, Savoia A, Benazzo M, Fierro T, Grolman W, Gresele P, Pecci A. Verver EJ, et al. Among authors: kunst hp. Ear Hear. 2016 Jan-Feb;37(1):112-20. doi: 10.1097/AUD.0000000000000198. Ear Hear. 2016. PMID: 26226608

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

Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research.

Kunst H, Marres H, Van Camp G, Cremers C. Kunst H, et al. Clin Otolaryngol Allied Sci. 1998 Feb;23(1):9-17. doi: 10.1046/j.1365-2273.1998.00093.x. Clin Otolaryngol Allied Sci. 1998. PMID: 9563659 Review. No abstract available.

5

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.

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

7

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

8

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

9

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

10

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.

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