Akar N - Search Results

1

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.

Tekin M, Hişmi BO, Fitoz S, Ozdağ H, Cengiz FB, Sirmaci A, Aslan I, Inceoğlu B, Yüksel-Konuk EB, Yilmaz ST, Yasun O, Akar N. Tekin M, et al. Among authors: akar n. Am J Hum Genet. 2007 Feb;80(2):338-44. doi: 10.1086/510920. Epub 2006 Dec 27. Am J Hum Genet. 2007. PMID: 17236138 Free PMC article.

2

Oxygen free radical-dependent increased platelet function in beta-thalassemia major patients.

Pasin M, Yavuzer S, Tekin M, Akar N, Violi F. Pasin M, et al. Among authors: akar n. Thromb Res. 1998 Dec 15;92(6):283-6. doi: 10.1016/s0049-3848(98)00129-7. Thromb Res. 1998. PMID: 9870895 No abstract available.

3

Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis.

Yalçinkaya F, Cakar N, Misirlioğlu M, Tümer N, Akar N, Tekin M, Taştan H, Koçak H, Ozkaya N, Elhan AH. Yalçinkaya F, et al. Among authors: akar n. Rheumatology (Oxford). 2000 Jan;39(1):67-72. doi: 10.1093/rheumatology/39.1.67. Rheumatology (Oxford). 2000. PMID: 10662876

4

Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis.

Tekin M, Yalçinkaya F, Tümer N, Akar N, Misirlioğlu M, Cakar N. Tekin M, et al. Among authors: akar n. Acta Paediatr. 2000 Feb;89(2):177-82. doi: 10.1080/080352500750028799. Acta Paediatr. 2000. PMID: 10709887 Clinical Trial.

5

MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis?

Tekin M, Yalçinkaya F, Cakar N, Akar N, Misirlioğlu M, Taştan H, Tümer N. Tekin M, et al. Among authors: akar n. Clin Genet. 2000 Jun;57(6):430-4. doi: 10.1034/j.1399-0004.2000.570605.x. Clin Genet. 2000. PMID: 10905662

6

Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients.

Yalçinkaya F, Tekin M, Cakar N, Akar E, Akar N, Tümer N. Yalçinkaya F, et al. Among authors: akar e, akar n. QJM. 2000 Oct;93(10):681-4. doi: 10.1093/qjmed/93.10.681. QJM. 2000. PMID: 11029479

7

Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemia.

Tekin D, Yavuzer S, Tekin M, Akar N, Cin S. Tekin D, et al. Among authors: akar n. Pediatr Int. 2001 Feb;43(1):74-7. doi: 10.1046/j.1442-200x.2001.01329.x. Pediatr Int. 2001. PMID: 11208005

8

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.

Tekin M, Akar N, Cin S, Blanton SH, Xia XJ, Liu XZ, Nance WE, Pandya A. Tekin M, et al. Among authors: akar n. Hum Genet. 2001 May;108(5):385-9. doi: 10.1007/s004390100507. Hum Genet. 2001. PMID: 11409864

9

Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome.

Cakar N, Yalçinkaya F, Ozkaya N, Tekin M, Akar N, Koçak H, Misirlioğlu M, Akar E, Tümer N. Cakar N, et al. Among authors: akar e, akar n. Clin Exp Rheumatol. 2001 Sep-Oct;19(5 Suppl 24):S63-7. Clin Exp Rheumatol. 2001. PMID: 11760404

10

Arthritis in children with familial Mediterranean fever.

Ince E, Cakar N, Tekin M, Kendirli T, Ozkaya N, Akar N, Yalçinkaya F. Ince E, et al. Among authors: akar n. Rheumatol Int. 2002 Apr;21(6):213-7. doi: 10.1007/s00296-001-0168-5. Rheumatol Int. 2002. PMID: 12036206

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