Baserer N - Search Results

1

Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss.

Uyguner O, Emiroglu M, Uzumcu A, Hafiz G, Ghanbari A, Baserer N, Yuksel-Apak M, Wollnik B. Uyguner O, et al. Among authors: baserer n. Clin Genet. 2003 Jul;64(1):65-9. doi: 10.1034/j.1399-0004.2003.00101.x. Clin Genet. 2003. PMID: 12791041

2

MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.

Kalay E, Uzumcu A, Krieger E, Caylan R, Uyguner O, Ulubil-Emiroglu M, Erdol H, Kayserili H, Hafiz G, Başerer N, Heister AJ, Hennies HC, Nürnberg P, Başaran S, Brunner HG, Cremers CW, Karaguzel A, Wollnik B, Kremer H. Kalay E, et al. Among authors: baserer n. Am J Med Genet A. 2007 Oct 15;143A(20):2382-9. doi: 10.1002/ajmg.a.31937. Am J Med Genet A. 2007. PMID: 17853461

3

The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family.

Uyguner O, Tukel T, Baykal C, Eris H, Emiroglu M, Hafiz G, Ghanbari A, Baserer N, Yuksel-Apak M, Wollnik B. Uyguner O, et al. Among authors: baserer n. Clin Genet. 2002 Oct;62(4):306-9. doi: 10.1034/j.1399-0004.2002.620409.x. Clin Genet. 2002. PMID: 12372058

4

Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.

Kalay E, Li Y, Uzumcu A, Uyguner O, Collin RW, Caylan R, Ulubil-Emiroglu M, Kersten FF, Hafiz G, van Wijk E, Kayserili H, Rohmann E, Wagenstaller J, Hoefsloot LH, Strom TM, Nürnberg G, Baserer N, den Hollander AI, Cremers FP, Cremers CW, Becker C, Brunner HG, Nürnberg P, Karaguzel A, Basaran S, Kubisch C, Kremer H, Wollnik B. Kalay E, et al. Among authors: baserer n. Hum Mutat. 2006 Jul;27(7):633-9. doi: 10.1002/humu.20368. Hum Mutat. 2006. PMID: 16752389

5

A novel homozygous COL11A2 deletion causes a C-terminal protein truncation with incomplete mRNA decay in a Turkish patient.

Kayserili H, Wollnik B, Güven G, Emiroğlu MU, Başerer N, Uyguner ZO. Kayserili H, et al. Among authors: baserer n. Am J Med Genet A. 2011 Jan;155A(1):180-5. doi: 10.1002/ajmg.a.33780. Am J Med Genet A. 2011. PMID: 21204229

6

The functional and oncologic effectiveness of near-total laryngectomy.

Aslan I, Baserer N, Yazicioglu E, Biliciler N, Hafiz G, Tinaz M, Kiyak E. Aslan I, et al. Among authors: baserer n. Am J Otolaryngol. 2002 Jul-Aug;23(4):196-202. doi: 10.1053/ajot.2002.123460. Am J Otolaryngol. 2002. PMID: 12105783

7

Management of carotid artery invasion in advanced malignancies of head and neck comparison of techniques.

Aslan I, Hafiz G, Baserer N, Yazicioglu E, Kiyak E, Tinaz M, Biliciler N. Aslan I, et al. Among authors: baserer n. Ann Otol Rhinol Laryngol. 2002 Sep;111(9):772-7. doi: 10.1177/000348940211100902. Ann Otol Rhinol Laryngol. 2002. PMID: 12296329

8

The site of the hearing loss in Refsum's disease.

Oysu C, Aslan I, Basaran B, Baserer N. Oysu C, et al. Among authors: baserer n. Int J Pediatr Otorhinolaryngol. 2001 Nov 1;61(2):129-34. doi: 10.1016/s0165-5876(01)00559-6. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11589979

9

Does the addition of hyperbaric oxygen therapy to the conventional treatment modalities influence the outcome of sudden deafness?

Aslan I, Oysu C, Veyseller B, Baserer N. Aslan I, et al. Among authors: baserer n. Otolaryngol Head Neck Surg. 2002 Feb;126(2):121-6. doi: 10.1067/mhn.2002.121915. Otolaryngol Head Neck Surg. 2002. PMID: 11870340

10

Audiometric manifestations of Waardenburg's syndrome.

Oysu C, Baserer N, Tinaz M. Oysu C, et al. Among authors: baserer n. Ear Nose Throat J. 2000 Sep;79(9):704-9. Ear Nose Throat J. 2000. PMID: 11011489

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