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Results:
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Results: 25
Authors:
Yenicesu, I
Uckan, D
Cetin, M
Tuncer, AM
Tezcan, I
Gurgey, A
Citation: I. Yenicesu et al., Evaluation of coagulation in pediatric bone marrow transplantation patients, PEDIAT TRAN, 5(6), 2001, pp. 430-433
Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations
Authors:
Timur, AA
Gurgey, A
Aktuglu, G
Kavakli, K
Canatan, D
Olek, K
Caglayan, SH
Citation: Aa. Timur et al., Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations, HAEMOPHILIA, 7(5), 2001, pp. 475-481
Outcome of noncatheter-related thrombosis in children: Influence of underlying or coexisting factors
Authors:
Gurgey, A
Aslan, D
Citation: A. Gurgey et D. Aslan, Outcome of noncatheter-related thrombosis in children: Influence of underlying or coexisting factors, J PED H ONC, 23(3), 2001, pp. 159-164
Authors:
Cemeroglu, AP
Kocabas, CC
Coskun, T
Gurgey, A
Citation: Ap. Cemeroglu et al., Low serum carnitine concentrations in healthy children with iron deficiency anemia, PED HEM ONC, 18(8), 2001, pp. 491-495
Authors:
Tekinalp, G
Sarici, SU
Erdinc, AS
Gogus, S
Balci, S
Gurgey, A
Citation: G. Tekinalp et al., Lethal hydrops fetalis due to congenital dyserythropoietic anemia in a newborn: Association of a new skeletal abnormality, PED HEM ONC, 18(8), 2001, pp. 537-542
Authors:
Gurgey, A
Haznedaroglu, IC
Egesel, T
Buyukasik, Y
Ozcebe, OI
Sayinalp, N
Dundar, SV
Bayraktar, Y
Citation: A. Gurgey et al., Two common genetic thrombotic risk factors: Factor V Leiden and prothrombin G20210A in adult Turkish patients with thrombosis, AM J HEMAT, 67(2), 2001, pp. 107-111
Authors:
Kalkanoglu, HS
Coskun, T
Aydogdu, SD
Tokatli, A
Gurgey, A
Citation: Hs. Kalkanoglu et al., Factor V Leiden mutation in Turkish patients with homozygous cystathioninebeta-synthase deficiency, J INH MET D, 24(3), 2001, pp. 367-369
Authors:
Balta, G
Gurgey, A
Kudayarov, DK
Tunc, B
Altay, C
Citation: G. Balta et al., Evidence for the existence of the PAF acetylhydrolase mutation (Va1279Phe)in non-Japanese populations: A preliminary study in Turkey, Azerbaijan, and Kyrgyzstan, THROMB RES, 101(4), 2001, pp. 231-234
Authors:
Oner, R
Oner, C
Birben, E
Sozen, M
Gumruk, F
Gurgey, A
Altay, C
Citation: R. Oner et al., beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G -> A substitution at+22 relative to the beta-globin cap site, BR J HAEM, 115(1), 2001, pp. 90-94
Authors:
Ericson, KG
Fadeel, B
Nilsson-Ardnor, S
Soderhall, C
Samuelsson, A
Janka, G
Schneider, M
Gurgey, A
Yalman, N
Revesz, T
Egeler, RM
Jahnukainen, K
Storm-Mathiesen, I
Haraldsson, A
Poole, J
de Saint Basile, G
Nordenskjold, M
Henter, JI
Citation: Kg. Ericson et al., Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis, AM J HU GEN, 68(3), 2001, pp. 590-597
Authors:
Yenicesu, I
Sanli, C
Gurgey, A
Citation: I. Yenicesu et al., Idiopathic thrombocytopenic purpura in acute lymphocytic leukemia, PED HEM ONC, 17(8), 2000, pp. 719-720
Authors:
Oner, R
Gumruk, F
Acar, C
Oner, C
Gurgey, A
Altay, C
Citation: R. Oner et al., Molecular characterization of glucose-6-phosphate dehydrogenase deficiencyin Turkey, HAEMATOLOG, 85(3), 2000, pp. 320-321
Authors:
Oner, R
Birben, E
Acar, C
Oner, C
Kara, A
Gumruk, F
Gurgey, A
Altay, C
Citation: R. Oner et al., Molecular analysis of Turkish beta-thalassemia heterozygotes with normal Hb A(2) levels, HEMOGLOBIN, 24(3), 2000, pp. 195-201
Authors:
Gumruk, F
Mergen, H
Oner, R
Ozcebe, O
Sayinalp, N
Oner, C
Gurgey, A
Altay, C
Citation: F. Gumruk et al., beta-thalassemia intermedia associated with homozygosity for the -87 (C ->T) mutation in a Turkish family, HEMOGLOBIN, 24(1), 2000, pp. 23-29
Authors:
Gurgey, A
Kudayarov, DK
Tuncer, M
Parlak, H
Altay, C
Citation: A. Gurgey et al., The factor V Leiden and prothrombin G20210A mutations in Kirghiz population, THROMB HAEM, 84(2), 2000, pp. 356-356
Authors:
Egesel, T
Buyukasik, Y
Dundar, SV
Gurgey, A
Kirazli, S
Bayraktar, Y
Citation: T. Egesel et al., The role of natural anticoagulant deficiencies and factor V Leiden in the development of idiopathic portal vein thrombosis, J CLIN GAST, 30(1), 2000, pp. 66-71
Authors:
Uckan, D
Hicsonmez, G
Yetgin, S
Gurgey, A
Cetin, M
Karaagaoglu, E
Okur, H
Tuncer, AM
Citation: D. Uckan et al., CD34/CD117 co-expression in childhood acute leukemia, LEUK RES, 24(3), 2000, pp. 201-206
Authors:
Tanyel, FC
Ocal, T
Balkanci, F
Cekirge, S
Senocak, ME
Buyukpamukcu, N
Gurgey, A
Citation: Fc. Tanyel et al., The factor V Leiden mutation: A possible contributor to the hepatic arterythrombosis encountered after liver transplantation in a child, J PED SURG, 35(4), 2000, pp. 607-609
Authors:
Togrul, J
Rustamov, R
Gurgey, A
Altay, S
Altay, C
Citation: J. Togrul et al., Prevalence of the prothrombin gene G20210A mutation in Azerbaijan, BR J HAEM, 108(4), 2000, pp. 887-888
Authors:
Kalayci, D
Gurgey, A
Guven, D
Parlak, H
Hasiripi, H
Citation: D. Kalayci et al., Factor V Leiden and prothrombin 20210 A mutations in patients with centraland branch retinal vein occlusion, ACT OPHTH S, 77(6), 1999, pp. 622-624
Authors:
Oner, AF
Gurgey, A
Kirazli, S
Okur, H
Tunc, B
Citation: Af. Oner et al., Changes of hemostatic factors in children with acute lymphoblastic leukemia receiving combined chemotherapy including high dose methylprednisolone and L-asparaginase, LEUK LYMPH, 33(3-4), 1999, pp. 361-364
Authors:
Gurgey, A
Citation: A. Gurgey, Clinical manifestations in thrombotic children with factor V Leiden mutation, PED HEM ONC, 16(3), 1999, pp. 233-237
Authors:
Gurakan, F
Gurgey, A
Bakkaloglu, A
Kocak, N
Citation: F. Gurakan et al., Homozygous factor V Leiden mutation in a child with Budd-Chiari syndrome, J PED GASTR, 28(5), 1999, pp. 516-517
Authors:
Ricciardone, MD
Ozcelik, T
Cevher, B
Ozdag, H
Tuncer, M
Gurgey, A
Uzunalimoglu, O
Cetinkaya, H
Tanyeli, A
Erken, E
Ozturk, M
Citation: Md. Ricciardone et al., Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1, CANCER RES, 59(2), 1999, pp. 290-293
Authors:
Sayinalp, N
Ozcebe, OI
Kirazli, S
Dogan, R
Dundar, SV
Gurgey, A
Citation: N. Sayinalp et al., Paget-Schroetter syndrome associated with FV : Q(506) and prothrombin 20210A - A case report, ANGIOLOGY, 50(8), 1999, pp. 689-692
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