Akar E - Search Results

1

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.

Tekin M, Doğu F, Taçyíldiz N, Akar E, Ikincioğullari A, Oğur G, Yavuz G, Babacan E, Akar N. Tekin M, et al. Among authors: akar e, akar n. Clin Genet. 2002 Jul;62(1):84-8. doi: 10.1034/j.1399-0004.2002.620112.x. Clin Genet. 2002. PMID: 12123493

2

Methylenetetrahydrofolate-dehydrogenase 1958 G-A (R653 Q) polymorphism in Turkish patients with venous thromboembolism.

Akar N, Akar E. Akar N, et al. Among authors: akar e. Acta Haematol. 1999;102(4):199-200. doi: 10.1159/000041015. Acta Haematol. 1999. PMID: 10725763 No abstract available.

3

Serum amyloid A1 -13 T/C alleles in Turkish familial Mediterranean fever patients with and without amyloidosis.

Akar N, Hasipek M, Oztürk A, Akar E, Tekin M. Akar N, et al. Among authors: akar e. J Nephrol. 2006 May-Jun;19(3):318-21. J Nephrol. 2006. PMID: 16874691

4

Search for genetic factors favoring thrombosis in Turkish population.

Akar N, Akar E, Misirlioğlu M, Avcu F, Yalçin A, Cin S. Akar N, et al. Among authors: akar e. Thromb Res. 1998 Oct 15;92(2):79-82. doi: 10.1016/s0049-3848(98)00113-3. Thromb Res. 1998. PMID: 9792115

5

Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct.

Akar N, Yilmaz E, Akar E, Deda G, Sipahi T. Akar N, et al. Among authors: akar e. Haemostasis. 2000 May-Jun;30(3):118-22. doi: 10.1159/000022533. Haemostasis. 2000. PMID: 11014961

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

Is the Ala138Gly alteration of MEFV gene important for amyloidosis?

Akar E, Yalcinkaya F, Akar N. Akar E, et al. Among authors: akar n. Hum Mutat. 2001;17(1):71. doi: 10.1002/1098-1004(2001)17:1<71::AID-HUMU8>3.0.CO;2-3. Hum Mutat. 2001. PMID: 11139244

8

Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction.

Gülec S, Aras O, Akar E, Tutar E, Omürlü K, Avci F, Dinçer I, Akar N, Oral D. Gülec S, et al. Among authors: akar e, akar n. Clin Cardiol. 2001 Apr;24(4):281-4. doi: 10.1002/clc.4960240405. Clin Cardiol. 2001. PMID: 11303694 Free PMC article.

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

First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY-ARG) and beta thalassemia (-29 G>A)- hemoglobin Hamadan combination in a Turkish family.

Akar E, Ozdemir S, Hakki Timur I, Akar N. Akar E, et al. Among authors: akar n. Am J Hematol. 2003 Dec;74(4):280-2. doi: 10.1002/ajh.10404. Am J Hematol. 2003. PMID: 14635211 Free article.

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