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收藏Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis
Rudd, 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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收藏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
Berber, 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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收藏Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia
Balta, G; Yuksek, N; Ozyurek, E; Ertem, U; Hicsonmez, G; Altay, C; Gurgey, A
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收藏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
Yetgin, 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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