Deda G - Search Results

1

Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct.

Akar N, Akar E, Deda G, Sipahi T, Orsal A. Akar N, et al. Among authors: deda g. J Child Neurol. 1999 Nov;14(11):749-51. doi: 10.1177/088307389901401113. J Child Neurol. 1999. PMID: 10593555

2

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: deda g. 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.

3

Coexistence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients.

Akar N, Akar E, Deda G, Sipahi T, Ezer U. Akar N, et al. Among authors: deda g. Pediatr Hematol Oncol. 1999 Nov-Dec;16(6):565-6. doi: 10.1080/088800199276886. Pediatr Hematol Oncol. 1999. PMID: 10599099 No abstract available.

4

Spina bifida and common mutations at the homocysteine metabolism pathway.

Akar N, Akar E, Deda G, Arsan S. Akar N, et al. Among authors: deda g. Clin Genet. 2000 Mar;57(3):230-1. doi: 10.1034/j.1399-0004.2000.570310.x. Clin Genet. 2000. PMID: 10782931 No abstract available.

5

No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke.

Akar N, Akar E, Deda G, Sipahi T. Akar N, et al. Among authors: deda g. Neurology. 2000 Aug 8;55(3):460-1. doi: 10.1212/wnl.55.3.460-a. Neurology. 2000. PMID: 10932305 No abstract available.

6

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: deda g. Haemostasis. 2000 May-Jun;30(3):118-22. doi: 10.1159/000022533. Haemostasis. 2000. PMID: 11014961

7

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: deda g. Thromb Res. 2001 Apr 15;102(2):115-20. doi: 10.1016/s0049-3848(01)00226-2. Thromb Res. 2001. PMID: 11323021

8

The alpha2 Gene alleles of the platelet collagen receptor integrin alpha2 beta1 in Turkish children with cerebral infarct.

Akar N, Duman T, Akar E, Deda G, Sipahi T. Akar N, et al. Among authors: deda g. Thromb Res. 2001 Apr 15;102(2):121-3. doi: 10.1016/s0049-3848(01)00228-6. Thromb Res. 2001. PMID: 11323022

9

Plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish children with cerebral infarct and effect on factor V 1691 A mutation.

Akar N, Akar E, Yilmaz E, Deda G. Akar N, et al. Among authors: deda g. J Child Neurol. 2001 Apr;16(4):294-5. doi: 10.1177/088307380101600413. J Child Neurol. 2001. PMID: 11332466

10

Hypopotassemic paralysis: a rare presentation of proximal renal tubular acidosis.

Deda G, Ekim M, Güven A, Karagöl U, Tümer N. Deda G, et al. J Child Neurol. 2001 Oct;16(10):770-1. doi: 10.1177/088307380101601013. J Child Neurol. 2001. PMID: 11669354

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