Huygen P - Search Results

1

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. Among authors: huygen p. Audiology. 1999 May-Jun;38(3):165-73. doi: 10.3109/00206099909073018. Audiology. 1999. PMID: 10437687 Review.

2

Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1-2q23.3.

van Beelen E, Schraders M, Huygen PL, Oostrik J, Plantinga RF, van Drunen W, Collin RW, Kooper DP, Pennings RJ, Cremers CW, Kremer H, Kunst HP. van Beelen E, et al. Among authors: huygen pl. Hear Res. 2013 Jun;300:10-7. doi: 10.1016/j.heares.2013.03.007. Epub 2013 Mar 26. Hear Res. 2013. PMID: 23538131

3

Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 family.

De Leenheer EM, Huygen PL, Coucke PJ, Admiraal RJ, van Camp G, Cremers CW. De Leenheer EM, et al. Ann Otol Rhinol Laryngol. 2002 Mar;111(3 Pt 1):267-74. doi: 10.1177/000348940211100312. Ann Otol Rhinol Laryngol. 2002. PMID: 11915881

4

Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study.

Bom SJ, Van Camp G, Cryns K, Admiraal RJ, Huygen PL, Cremers CW. Bom SJ, et al. Otol Neurotol. 2002 Nov;23(6):876-84. doi: 10.1097/00129492-200211000-00012. Otol Neurotol. 2002. PMID: 12438850

5

Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).

Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW. Pennings RJ, et al. Arch Otolaryngol Head Neck Surg. 2003 Apr;129(4):421-6. doi: 10.1001/archotol.129.4.421. Arch Otolaryngol Head Neck Surg. 2003. PMID: 12707188

6

Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.

Pennings RJ, Huygen PL, van den Ouweland JM, Cryns K, Dikkeschei LD, Van Camp G, Cremers CW. Pennings RJ, et al. Audiol Neurootol. 2004 Jan-Feb;9(1):51-62. doi: 10.1159/000074187. Audiol Neurootol. 2004. PMID: 14676474

7

Evidence of progression and fluctuation of hearing impairment in branchio-oto-renal syndrome.

Kemperman MH, Koch SM, Kumar S, Huygen PL, Joosten FB, Cremers CW. Kemperman MH, et al. Among authors: huygen pl. Int J Audiol. 2004 Oct;43(9):523-32. doi: 10.1080/14992020400050067. Int J Audiol. 2004. PMID: 15726843

8

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. Among authors: huygen p. 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.

9

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. Among authors: huygen p. Laryngoscope. 1998 Jan;108(1 Pt 1):74-80. doi: 10.1097/00005537-199801000-00014. Laryngoscope. 1998. PMID: 9432071

10

Hearing impairment related to age in Usher syndrome types 1B and 2A.

Wagenaar M, van Aarem A, Huygen P, Pieke-Dahl S, Kimberling W, Cremers C. Wagenaar M, et al. Among authors: huygen p. Arch Otolaryngol Head Neck Surg. 1999 Apr;125(4):441-5. doi: 10.1001/archotol.125.4.441. Arch Otolaryngol Head Neck Surg. 1999. PMID: 10208682

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