Deda G - Search Results

1

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.

Dönmez-Demir B, Celkan T, Sarper N, Deda G, İnce E, Çalişkan Ü, Öztürk G, Karagün B, Küpesiz A, Tokgöz H, Akar N, Özdağ H. Dönmez-Demir B, et al. Among authors: deda g. Blood Coagul Fibrinolysis. 2016 Sep;27(6):637-44. doi: 10.1097/MBC.0000000000000383. Blood Coagul Fibrinolysis. 2016. PMID: 26340456

2

Excitatory amino acid levels in cerebrospinal fluid of patients with infantile spasms.

Ince E, Karagöl U, Deda G. Ince E, et al. Among authors: deda g. Acta Paediatr. 1997 Dec;86(12):1333-6. doi: 10.1111/j.1651-2227.1997.tb14908.x. Acta Paediatr. 1997. PMID: 9475311 Clinical Trial.

3

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.

4

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

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

6

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

7

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

8

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

9

Recurrent arterial thrombosis in a child: primary antiphospholipid antibody syndrome.

Uysal Z, Doğu F, Kürekçi AE, Culha VK, Deda G, Ekim M, Akar N, Erterm M, Ikincioğullari A, Babacan E, Gözdaşoğlu S. Uysal Z, et al. Among authors: deda g. Pediatr Hematol Oncol. 2002 Jan-Feb;19(1):59-66. doi: 10.1080/088800102753356202. Pediatr Hematol Oncol. 2002. PMID: 11787868

10

Combined genetic defects in a child with ischemic stroke: case report.

Deda G, Içağasioğlu D, Caksen H, Akar N. Deda G, et al. J Child Neurol. 2002 Jul;17(7):533-4. doi: 10.1177/088307380201700711. J Child Neurol. 2002. PMID: 12269733

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