Kunst HPM - Search Results

1

Hearing aid fitting for visual and hearing impaired patients with Usher syndrome type IIa.

Hartel BP, Agterberg MJH, Snik AF, Kunst HPM, van Opstal AJ, Bosman AJ, Pennings RJE. Hartel BP, et al. Among authors: kunst hpm. Clin Otolaryngol. 2017 Aug;42(4):805-814. doi: 10.1111/coa.12775. Epub 2016 Nov 6. Clin Otolaryngol. 2017. PMID: 27759911 Free PMC article.

2

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. 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

3

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.

Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ. Plantinga RF, et al. J Assoc Res Otolaryngol. 2007 Mar;8(1):1-7. doi: 10.1007/s10162-006-0060-9. Epub 2006 Nov 30. J Assoc Res Otolaryngol. 2007. PMID: 17136632 Free PMC article.

4

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.

Hogewind BF, Pennings RJ, Hol FA, Kunst HP, Hoefsloot EH, Cruysberg JR, Cremers CW. Hogewind BF, et al. Mol Vis. 2010 Jan 12;16:26-35. Mol Vis. 2010. PMID: 20069065 Free PMC article.

5

Ear and hearing problems in relation to karyotype in children with Turner syndrome.

Verver EJ, Freriks K, Thomeer HG, Huygen PL, Pennings RJ, Alfen-van der Velden AA, Timmers HJ, Otten BJ, Cremers CW, Kunst HP. Verver EJ, et al. Hear Res. 2011 May;275(1-2):81-8. doi: 10.1016/j.heares.2010.12.007. Epub 2010 Dec 10. Hear Res. 2011. PMID: 21147207

6

Phenotype of the first otosclerosis family linked to OTSC10.

Weegerink NJ, Schrauwen I, Huygen PL, Pennings RJ, Cremers CW, Van Camp G, Kunst HP. Weegerink NJ, et al. Laryngoscope. 2011 Apr;121(4):838-45. doi: 10.1002/lary.21463. Laryngoscope. 2011. PMID: 21433022

7

Phenotypes of two Dutch DFNA3 families with mutations in GJB2.

Weegerink NJ, Pennings RJ, Huygen PL, Hoefsloot LH, Cremers CW, Kunst HP. Weegerink NJ, et al. Ann Otol Rhinol Laryngol. 2011 Mar;120(3):191-7. doi: 10.1177/000348941112000308. Ann Otol Rhinol Laryngol. 2011. PMID: 21510145

8

Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment.

Schraders M, Haas SA, Weegerink NJ, Oostrik J, Hu H, Hoefsloot LH, Kannan S, Huygen PL, Pennings RJ, Admiraal RJ, Kalscheuer VM, Kunst HP, Kremer H. Schraders M, et al. Am J Hum Genet. 2011 May 13;88(5):628-34. doi: 10.1016/j.ajhg.2011.04.012. Epub 2011 May 5. Am J Hum Genet. 2011. PMID: 21549342 Free PMC article.

9

Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations.

Weegerink NJ, Schraders M, Oostrik J, Huygen PL, Strom TM, Granneman S, Pennings RJ, Venselaar H, Hoefsloot LH, Elting M, Cremers CW, Admiraal RJ, Kremer H, Kunst HP. Weegerink NJ, et al. J Assoc Res Otolaryngol. 2011 Dec;12(6):753-66. doi: 10.1007/s10162-011-0282-3. Epub 2011 Jul 23. J Assoc Res Otolaryngol. 2011. PMID: 21786053 Free PMC article.

10

Audiometric characteristics of a Dutch family with Muckle-Wells syndrome.

Weegerink NJ, Schraders M, Leijendeckers J, Slieker K, Huygen PL, Hoefsloot L, Oostrik J, Pennings RJ, Simon A, Snik A, Kremer H, Kunst HP. Weegerink NJ, et al. Hear Res. 2011 Dec;282(1-2):243-51. doi: 10.1016/j.heares.2011.07.006. Epub 2011 Jul 23. Hear Res. 2011. PMID: 21810457

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