Akar E - Search Results

1

Endothelial cell protein C receptor (EPCR) gene exon III, 23 bp insertion mutation in the Turkish pediatric thrombotic patients.

Akar N, Gökdemir R, Ozel D, Akar E. Akar N, et al. Among authors: akar e. Thromb Haemost. 2002 Dec;88(6):1068-9. Thromb Haemost. 2002. PMID: 12529763 No abstract available.

2

Frequency of Factor V (1691 G --> A) mutation in Turkish population.

Akar N, Akar E, Dalgin G, Sözüöz A, Omürlü K, Cin S. Akar N, et al. Among authors: akar e. Thromb Haemost. 1997 Dec;78(6):1527-8. Thromb Haemost. 1997. PMID: 9423807 No abstract available.

3

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

4

Endothelial nitric oxide synthase intron 4, 27 bp repeat polymorphism in Turkish patients with deep vein thrombosis and cerebrovascular accidents.

Akar N, Akar E, Cin S, Deda G, Avcu F, Yalçin A. Akar N, et al. Among authors: akar e. Thromb Res. 1999 Apr 1;94(1):63-4. doi: 10.1016/s0049-3848(98)00193-5. Thromb Res. 1999. PMID: 10213182 No abstract available.

5

Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thrombotic patients with and without FV1691 G-A.

Akar N, Yilmaz E, Akar E, Avcu F, Yalçin A, Cin S. Akar N, et al. Among authors: akar e. Thromb Res. 2000 Feb 15;97(4):227-30. doi: 10.1016/s0049-3848(99)00164-4. Thromb Res. 2000. PMID: 10674409

6

Effect of methylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients.

Akar N, Akar E, Akçay R, Avcu F, Yalcin A, Cin S. Akar N, et al. Among authors: akar e. Thromb Res. 2000 Feb 1;97(3):163-7. doi: 10.1016/s0049-3848(99)00157-7. Thromb Res. 2000. PMID: 10680647

7

Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in turkish thromboembolic patients.

Akar N, Akar E, Yilmaz E. Akar N, et al. Among authors: akar e. Am J Hematol. 2000 Sep;65(1):88. doi: 10.1002/1096-8652(200009)65:1<88::aid-ajh19>3.0.co;2-0. Am J Hematol. 2000. PMID: 10936874 Free article. No abstract available.

8

Common mutations at the homocysteine metabolism pathway and pediatric stroke.

Akar N, Akar E, Ozel D, Deda G, Sipahi T. Akar N, et al. Among authors: akar e. Thromb Res. 2001 Apr 15;102(2):115-20. doi: 10.1016/s0049-3848(01)00226-2. Thromb Res. 2001. PMID: 11323021

9

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.

10

Prothrombin gene 20210 G-A mutation in the Turkish population.

Akar N, Misirlioğlu M, Akar E, Avcu F, Yalçin A, Sözüöz A. Akar N, et al. Among authors: akar e. Am J Hematol. 1998 Jul;58(3):249. doi: 10.1002/(sici)1096-8652(199807)58:3<249::aid-ajh20>3.0.co;2-3. Am J Hematol. 1998. PMID: 9662283 Free article. No abstract available.

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