Marres HA - 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: marres ha. 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

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

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

6

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

7

Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers.

Marres HA, Cremers CW. Marres HA, et al. Arch Otolaryngol Head Neck Surg. 1989 May;115(5):591-5. doi: 10.1001/archotol.1989.01860290049013. Arch Otolaryngol Head Neck Surg. 1989. PMID: 2706105

8

The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees.

Marres HA, Cremers CW, Dixon MJ, Huygen PL, Joosten FB. Marres HA, et al. Arch Otolaryngol Head Neck Surg. 1995 May;121(5):509-14. doi: 10.1001/archotol.1995.01890050009002. Arch Otolaryngol Head Neck Surg. 1995. PMID: 7727083 Free article.

9

Hearing loss in the Saethre-Chotzen syndrome.

Ensink RJ, Marres HA, Brunner HG, Cremers CW. Ensink RJ, et al. Among authors: marres ha. J Laryngol Otol. 1996 Oct;110(10):952-7. doi: 10.1017/s0022215100135443. J Laryngol Otol. 1996. PMID: 8977861

10

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: marres ha. 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

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