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Results:
1-16
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Results: 16
Authors:
Sipahi, T
Duru, F
Yarah, N
Akar, N
Citation: T. Sipahi et al., Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome, EUR J PED, 160(3), 2001, pp. 198-198
Authors:
Uckun, A
Sipahi, T
Igde, M
Uner, C
Cakmak, O
Citation: A. Uckun et al., Is it possible to diagnose Rapunzel syndrome pre-operatively?, EUR J PED, 160(11), 2001, pp. 682-683
Authors:
Sipahi, T
Akar, N
Dincer, N
Egin, Y
Cin, S
Citation: T. Sipahi et al., Serum interleukin-2 and interleukin-6 levels in zinc deficiency, J TROP PEDI, 47(2), 2001, pp. 120-122
Authors:
Sipahi, T
Akar, N
Dincer, N
Cin, S
Citation: T. Sipahi et al., Plasma zinc levels in patients with iron-deficiency anemia, J TROP PEDI, 47(2), 2001, pp. 122-123
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:
Karakurt, C
Sipahi, T
Ceylaner, S
Senocak, F
Karademir, S
Becer, M
Citation: C. Karakurt et al., Cutis laxa with growth and developmental delay, CLIN PEDIAT, 40(7), 2001, pp. 422-423
Authors:
Sahin, F
Sipahi, T
Dogan, H
Oksal, A
Ertan, O
Citation: F. Sahin et al., Pathological case of the month, ARCH PED AD, 154(11), 2000, pp. 1165-1166
Authors:
Yarali, N
Duru, F
Sipahi, T
Kara, A
Tezic, T
Citation: N. Yarali et al., Parvovirus B19 infection reminiscent of myelodysplastic syndrome in three children with chronic hemolytic anemia, PED HEM ONC, 17(6), 2000, pp. 475-482
Authors:
Sipahi, T
Uner, C
Yildiz, YT
Akar, N
Citation: T. Sipahi et al., Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis, PEDIAT RAD, 30(6), 2000, pp. 420-423
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
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:
Kucuk, NO
Aras, G
Sipahi, T
Ibis, E
Akar, N
Soylu, A
Erbay, G
Citation: No. Kucuk et al., Evaluation of cardiac functions in patients with thalassemia major, ANN NUCL M, 13(3), 1999, pp. 175-179
Authors:
Sipahi, T
Duru, F
Ciftci, E
Sahin, F
Akar, N
Citation: T. Sipahi et al., Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence, EUR J HAEMA, 62(4), 1999, pp. 281-283
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:
Sipahi, T
Okumus, N
Sahin, F
Kuyucu, N
Tan, E
Gurer, Y
Citation: T. Sipahi et al., Congenital insensitivity to pain with anhidrosis: report of a 68-day-old case, EUR J PED, 158(3), 1999, pp. 268-269
Risultati:
1-16
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