Apaydin F - Search Results

1

Clinical evidence for dystrophin dysfunction as a cause of hearing loss in locus DFN4.

Pfister MH, Apaydin F, Turan O, Bereketoglu M, Bilgen V, Braendle U, Kose S, Zenner HP, Lalwani AK. Pfister MH, et al. Among authors: apaydin f. Laryngoscope. 1999 May;109(5):730-5. doi: 10.1097/00005537-199905000-00010. Laryngoscope. 1999. PMID: 10334222

2

A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD.

Pfister MH, Apaydin F, Turan O, Bereketoglu M, Bylgen V, Braendle U, Zenner HP, Lalwani AK. Pfister MH, et al. Among authors: apaydin f. Genomics. 1998 Nov 1;53(3):377-82. doi: 10.1006/geno.1998.5538. Genomics. 1998. PMID: 9799605

3

[Genetic sensorineural hearing loss in childhood].

Turan O, Apaydin F. Turan O, et al. Among authors: apaydin f. Kulak Burun Bogaz Ihtis Derg. 2002 Mar-Apr;9(2):99-105. Kulak Burun Bogaz Ihtis Derg. 2002. PMID: 12122638 Free article. Turkish.

4

[The incidence of Usher's syndrome and its clinical types].

Bereketoğlu M, Avşar EU, Turan O, Afrashi F, Apaydin F. Bereketoğlu M, et al. Among authors: apaydin f. Kulak Burun Bogaz Ihtis Derg. 2002 Jan-Feb;9(1):15-20. Kulak Burun Bogaz Ihtis Derg. 2002. PMID: 12122620 Free article. Turkish.

5

A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.

Leal SM, Apaydin F, Barnwell C, Iber M, Kandogan T, Pfister M, Braendle U, Cura O, Schwalb M, Zenner HP, Vitale E. Leal SM, et al. Among authors: apaydin f. Eur J Hum Genet. 1998 Jul-Aug;6(4):341-4. doi: 10.1038/sj.ejhg.5200201. Eur J Hum Genet. 1998. PMID: 9781041 Free PMC article.

6

[Waardenburg syndrome. A heterogenic disorder with variable penetrance].

Apaydin F, Bereketoglu M, Turan O, Hribar K, Maassen MM, Günhan O, Zenner HP, Pfister M. Apaydin F, et al. HNO. 2004 Jun;52(6):533-7. doi: 10.1007/s00106-003-0938-3. HNO. 2004. PMID: 15029423 German.

7

[Hereditary deafness in Turkey. Initial results].

Apaydin F, Pfister M, Iber M, Kandogan T, Leal SM, Brändle U, Cura O, Zenner HP. Apaydin F, et al. HNO. 1998 Sep;46(9):809-14. doi: 10.1007/s001060050317. HNO. 1998. PMID: 9816535 Free PMC article. German.

8

Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness.

Mirghomizadeh F, Pfister M, Apaydin F, Petit C, Kupka S, Pusch CM, Zenner HP, Blin N. Mirghomizadeh F, et al. Among authors: apaydin f. Neurobiol Dis. 2002 Jul;10(2):157-64. doi: 10.1006/nbdi.2002.0488. Neurobiol Dis. 2002. PMID: 12127154

9

A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.

Pfister M, Thiele H, Van Camp G, Fransen E, Apaydin F, Aydin O, Leistenschneider P, Devoto M, Zenner HP, Blin N, Nürnberg P, Ozkarakas H, Kupka S. Pfister M, et al. Among authors: apaydin f. Cell Physiol Biochem. 2004;14(4-6):369-76. doi: 10.1159/000080347. Cell Physiol Biochem. 2004. PMID: 15319541

10

A patient database application for Hereditary Deafness Epidemiology and Clinical Research (H.E.A.R.): an effort for standardization in multiple languages.

Pfister M, Akyildiz S, Gunhan O, Maassen M, Rodriguez JJ, Zenner HP, Apaydin F. Pfister M, et al. Among authors: apaydin f. Eur Arch Otorhinolaryngol. 2003 Feb;260(2):81-5. doi: 10.1007/s00405-002-0529-z. Epub 2002 Sep 27. Eur Arch Otorhinolaryngol. 2003. PMID: 12582784

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