Huygen PL - Search Results

1

Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472.

Ensink RJ, Verhoeven K, Marres HA, Huygen PL, Padberg GW, ter Laak H, van Camp G, Willems PJ, Cremers CW. Ensink RJ, et al. Among authors: huygen pl. Arch Otolaryngol Head Neck Surg. 1998 Aug;124(8):886-91. doi: 10.1001/archotol.124.8.886. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9708714

2

The clinical spectrum of maternally transmitted hearing loss.

Ensink RJ, Huygen PL, Cremers CW. Ensink RJ, et al. Among authors: huygen pl. Adv Otorhinolaryngol. 2002;61:172-83. doi: 10.1159/000066831. Adv Otorhinolaryngol. 2002. PMID: 12408082 No abstract available.

3

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. Among authors: huygen pl. 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

4

A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.

Kemperman MH, De Leenheer EM, Huygen PL, van Wijk E, van Duijnhoven G, Cremers FP, Kremer H, Cremers CW. Kemperman MH, et al. Among authors: huygen pl. Arch Otolaryngol Head Neck Surg. 2004 Mar;130(3):281-8. doi: 10.1001/archotol.130.3.281. Arch Otolaryngol Head Neck Surg. 2004. PMID: 15023833

5

Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.

Pauw RJ, van Drunen FJ, Collin RW, Huygen PL, Kremer H, Cremers CW. Pauw RJ, et al. Among authors: huygen pl. Arch Otolaryngol Head Neck Surg. 2008 Mar;134(3):294-300. doi: 10.1001/archotol.134.3.294. Arch Otolaryngol Head Neck Surg. 2008. PMID: 18347256

6

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.

7

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

8

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. 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

9

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

10

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

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