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Aytemiz Gürgey

national institutes of health (nih) - usa

38H指数
310论文数
5.2K被引数
收录论文 26
发表时间
Hemophagocytosis associated with leukemia: a striking association with juvenile myelomonocytic leukemia与白血病相关的噬血细胞症: 与青少年粒单核细胞白血病的惊人联系
err2009-10-02
err13
PREAI
errUnal, Sule; Cetin, Mualla; Kutlay, Nuket Yurur; Elmas, Selin Aytac; Gumruk, Fatma; Tukun, Ajlan; Tuncer, Murat; Gurgey, Aytemiz
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Molecular pathology of haemophilia A in Turkish patients:: identification of 36 independent mutations
err2008-07-07
err10
PREAI
errTimur, AA; Gürgey, A; Aktuglu, G; Kavakli, K; Canatan, D; Olek, K; Çaglayan, SH
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Lymphocytic vacuolization in sialic acid storage disease
err2007-11-29
err1
errOAAI
errKuskonmaz, Baris; Unal, Sule; Cordukcu, Emine; Aydin, Halil; Coskun, Turgay; Gurgey, Aytemiz; Gumruk, Fatma
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Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis
err2007-10-22
err54
PREAI
errRudd, E.; Bryceson, Y. T.; Zheng, C.; Edner, J.; Wood, S. M.; Ramme, K.; Gavhed, S.; Gurgey, A.; Hellebostad, M.; Bechensteen, A. G.; Ljunggren, H-G; Fadeel, B.; Nordenskjold, M.; Henter, J-I
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Further hemolytic disease of the newborn caused by anti-M
err2007-03-02
err6
PREAI
errKanra, T; Erdem, G; Tekinalp, G; Gurgey, A; Yigit, S; Dogru, D
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Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N
err2006-06-23
err9
PREAI
errBerber, E.; Fidanci, I. D.; Un, C.; El-Maarri, O.; Aktuglu, G.; Gurgey, A.; Celkan, T.; Meral, A.; Oldenburg, J.; Graw, J.; Akar, N.; Caglayan, H.
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Outcome in children with purpura fulminans:: Report on 16 patients
err2005-09-01
err22
errOAAI
errGürgey, A; Aytac, S; Kanra, G; Secmeer, G; Ceyhan, M; Altay, C
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Evaluation of thrombotic children with malignancy
err2005-02-26
err31
PREAI
errÜnal, S; Varan, A; Yalçin, B; Büyükpamukcu, M; Gürgey, A
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Severe hemolytic anemia associated with Hb Volga [β27(β9)Ala→Asp]:: GCC→GAC at codon 27 in a Turkish family
err2004-07-23
err6
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errSözen, M; Karaaslan, C; Öner, R; Gümrük, F; Özdemir, MA; Altay, C; Gürgey, A; Öner, C
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Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia
err2003-06-20
err93
errOAAI
errBalta, G; Yuksek, N; Ozyurek, E; Ertem, U; Hicsonmez, G; Altay, C; Gurgey, A
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Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up
errLEUKEMIA
IF13.4
err2003-02-18
err33
PREAI
errYetgin, S; Tuncer, MA; Çetin, M; Gümrük, F; Yenicesu, I; Tunç, B; Öner, AF; Toksoy, H; Koç, A; Aslan, D; Özyorek, E; Olcay, L; Atahan, L; Tunçbilek, ET; Gürgey, A
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Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis
err2003-01-01
err23
PREAI
errEricson, KG; Fadeel, B; Andersson, M; Gudmundsson, GH; Gürgey, A; Yalman, N; Janka, G; Nordenskjöld, M; Henter, JI
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Griscelli disease:: Genotype-phenotype correlation in an array of clinical heterogeneity
err2002-01-01
err64
PREAI
errSanal, O; Ersoy, F; Tezcan, I; Metin, A; Yel, L; Ménasché, G; Gürgey, A; Berkel, I; de Saint Basile, G
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