Kunst HPM - Search Results

1

Cochlear Implantation in Patients With Usher Syndrome Type IIa Increases Performance and Quality of Life.

Hartel BP, van Nierop JWI, Huinck WJ, Rotteveel LJC, Mylanus EAM, Snik AF, Kunst HPM, Pennings RJE. Hartel BP, et al. Among authors: kunst hpm. Otol Neurotol. 2017 Jul;38(6):e120-e127. doi: 10.1097/MAO.0000000000001441. Otol Neurotol. 2017. PMID: 28498263

2

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.

3

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

4

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

5

Endolymphatic sac tumors: clinical outcome and management in a series of 9 cases.

Timmer FC, Neeskens LJ, van den Hoogen FJ, Slootweg PJ, Dunnebier EA, Pauw BK, Mulder JJ, Cremers CW, Kunst HP. Timmer FC, et al. Otol Neurotol. 2011 Jun;32(4):680-5. doi: 10.1097/MAO.0b013e318215992b. Otol Neurotol. 2011. PMID: 21451430

6

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

7

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.

8

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.

9

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

10

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. 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

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