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Results:
1-24
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Results: 24
Authors:
Unal, E
Cavdar, AO
Babacan, E
Gozdasoglu, S
Yavuz, G
Ikinciogullari, A
Akar, E
Cin, S
Citation: E. Unal et al., Zinc status and cytokine profile in pediatric Hodgkin's disease, J TR EL EXP, 14(1), 2001, pp. 25-30
Authors:
Akar, N
Akar, E
Yilmaz, E
Deda, G
Citation: N. Akar et al., Plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish children with cerebral infarct and effect on factor V 1691 A mutation, J CHILD NEU, 16(4), 2001, pp. 294-295
Authors:
Cakar, N
Yalcinkaya, F
Ozkaya, N
Tekin, M
Akar, N
Kocak, H
Misirlioglu, M
Akar, E
Tumer, N
Citation: N. Cakar et al., Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome, CLIN EXP RH, 19(5), 2001, pp. S63-S67
Authors:
Tutar, HE
Imamoglu, A
Kendirli, T
Akar, E
Atalay, S
Akar, N
Citation: He. Tutar et al., Isolated recurrent pericarditis in a patient with familial Mediterranean fever, EUR J PED, 160(4), 2001, pp. 264-265
Authors:
Gulec, S
Aras, O
Akar, E
Tutar, E
Omurlu, K
Avci, F
Dincer, I
Akar, N
Oral, D
Citation: S. Gulec et al., Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction, CLIN CARD, 24(4), 2001, pp. 281-284
Authors:
Akar, N
Akar, E
Ozel, D
Deda, G
Sipahi, T
Citation: N. Akar et al., Common mutations at the homocysteine metabolism pathway and pediatric stroke, THROMB RES, 102(2), 2001, pp. 115-120
Authors:
Akar, N
Duman, T
Akar, E
Deda, G
Sipahi, L
Citation: N. Akar et al., The alpha 2 gene alleles of the platelet collagen receptor integrin alpha 2 beta 1 in Turkish children with cerebral infarct, THROMB RES, 102(2), 2001, pp. 121-123
Authors:
Akar, N
Akar, E
Yalcinkaya, F
Citation: N. Akar et al., E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients, PEDIATRICS, 108(1), 2001, pp. 215-215
Authors:
Yalcinkaya, F
Tekin, M
Cakar, N
Akar, E
Akar, N
Tumer, N
Citation: F. Yalcinkaya et al., Familial Mediterranean fever and systemic amyloidosis in untreated Turkishpatients, QJM-MON J A, 93(10), 2000, pp. 681-684
Authors:
Akar, N
Akar, E
Yilmaz, E
Citation: N. Akar et al., Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in Turkishthromboembolic patients, AM J HEMAT, 65(1), 2000, pp. 88-88
Authors:
Akar, N
Akar, E
Yilmaz, E
Citation: N. Akar et al., Factor V (His 1299 Arg) in Turkish patients with venous thromboembolism, AM J HEMAT, 63(2), 2000, pp. 102-103
Authors:
Akar, N
Yilmaz, E
Akar, E
Deda, G
Sipahi, T
Citation: N. Akar et al., Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct, HAEMOSTASIS, 30(3), 2000, pp. 118-122
Authors:
Akar, N
Yilmaz, E
Akar, E
Avcu, F
Yalcin, A
Cin, S
Citation: N. Akar et al., Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thrombotic patients with and without FV1691 G-A, THROMB RES, 97(4), 2000, pp. 227-230
Authors:
Akar, N
Akar, E
Akcay, R
Avcu, F
Yalcin, A
Cin, S
Citation: N. Akar et al., Effect of metylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients, THROMB RES, 97(3), 2000, pp. 163-167
Authors:
Avcu, F
Akar, E
Demirkilic, U
Yilmaz, E
Akar, N
Yalcin, A
Citation: F. Avcu et al., The role of prothrombotic mutations in patients with Buerger's disease, THROMB RES, 100(3), 2000, pp. 143-147
Authors:
Akar, N
Akar, E
Deda, G
Sipahi, T
Citation: N. Akar et al., No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke, NEUROLOGY, 55(3), 2000, pp. 460-461
Authors:
Akar, N
Akar, E
Deda, G
Arsan, S
Citation: N. Akar et al., Spina bifida and common mutations at the homocysteine metabolism pathway, CLIN GENET, 57(3), 2000, pp. 230-231
Authors:
Avcu, F
Akar, N
Akar, E
Beyan, C
Yalcin, A
Citation: F. Avcu et al., Prothrombin gene 20210 G -> A and Factor V Arg 506 to Gln mutation in a patient with Buerger's disease - A case report, ANGIOLOGY, 51(5), 2000, pp. 421-423
Authors:
Akar, N
Yalcinkaya, F
Akar, E
Cakar, N
Citation: N. Akar et al., MEFV mutation analysis in Turkish familial Mediterranean fever patients with amyloidosis, AMYLOID, 6(4), 1999, pp. 301-302
Authors:
Akar, N
Akar, E
Deda, G
Sipahi, T
Ezer, U
Citation: N. Akar et al., 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, PED HEM ONC, 16(6), 1999, pp. 565-566
Authors:
Akar, N
Akar, E
Deda, G
Sipahi, T
Orsal, A
Citation: N. Akar et al., Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct, J CHILD NEU, 14(11), 1999, pp. 749-751
Authors:
Akar, N
Akar, E
Tastan, H
Citation: N. Akar et al., Feasibility of restriction enzyme protocols for the molecular diagnosis ofabnormal hemoglobins in Turkish population, AM J HEMAT, 62(3), 1999, pp. 198-198
Authors:
Akar, N
Akar, E
Cin, S
Deda, G
Avcu, F
Yalcin, A
Citation: N. Akar et al., Endothelial nitric oxide synthase intron 4, 27 bp repeat polymorphism in Turkish patients with deep vein thrombosis and cerebrovascular accidents, THROMB RES, 94(1), 1999, pp. 63-64
Authors:
Akar, N
Akar, E
Citation: N. Akar et E. Akar, Methylenetetrahydrofolate-dehydrogenase 1958 G-A (R653 Q) polymorphism in Turkish patients with venous thromboembolism, ACT HAEMAT, 102(4), 1999, pp. 199-200
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