Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis von Rudd, E, Bryceson, Y T, Zheng, C, Edner, J, Wood, S M, Ramme, K, Gavhed, S, Gürgey, A, Hellebostad, M, Bechensteen, A G, Ljunggren, H-G, Fadeel, B, Nordenskjöld, M, Henter, J-I

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Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis von Göransdotter Ericson, Kim, Fadeel, Bengt, Nilsson-Ardnor, Sofie, Söderhäll, Cilla, Samuelsson, AnnaCarin, Janka, Gritta, Schneider, Marion, Gürgey, Aytemiz, Yalman, Nevin, Révész, Tom, Egeler, R. Maarten, Jahnukainen, Kirsi, Storm-Mathiesen, Ingebjörg, Haraldsson, Ásgeir, Poole, Janet, de Saint Basile, Geneviève, Nordenskjöld, Magnus, Henter, Jan-Inge

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Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malign... von Rudd, E, Göransdotter Ericson, K, Zheng, C, Uysal, Z, Özkan, A, Gürgey, A, Fadeel, B, Nordenskjöld, M, Henter, J-I

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Importance of RDW value in differential diagnosis of hypochrome anemias von Aslan, D., Gümrük, F., Gürgey, A., Altay, Ç.

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Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1 von RICCIARDONE, M. D, ÖZCELIK, T, ÖZTÜRK, M, CEVHER, B, ÖZDAG, H, TUNCER, M, GÜRGEY, A, UZUNALIMOGLU, Ö, CETINKAYA, H, TANYELI, A, ERKEN, E

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Reply von Altay, C., Gürgey, 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... von Yetgin, S, Tuncer, M A, Çetin, M, Gümrük, F, Yenicesu, I, Tunç, B, Öner, A F, Toksoy, H, Koç, A, Aslan, D, Özyürek, E, Olcay, L, Atahan, L, Tunçbilek, E, Gürgey, A

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Primary Hemophagocytic Lymphohistiocytosis in Turkish Children von Gürgey, A., Gö ü, S., Özyürek, E., Aslan, D., Gümrük, F., Çetin, M., Yüce, A., Ceyhan, M., Seçmeer, G., Yetgin, S., Hiçsönmez, G.

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Diffusion-Weighted Cranial MR Imaging Findings in a Patient with Hemophagocytic Syndrome von Ozgen, B, Karli-Oguz, K, Sarikaya, B, Tavil, B, Gurgey, A

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MR findings in peliosis hepatis von SAATCI, I, COSKUN, M, BOYVAT, F, CILA, A, GÜRGEY, A

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The Role of Natural Anticoagulant Deficiencies and Factor V Leiden in the Development of Idiopathic Portal Vein Thrombosis von Egesel, Türker, Büyükaṣk, Yahya, Dündar, Semra V, Gürgey, Aytemiz, Kirazl, Ṣerafettin, Bayraktar, Yusuf

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Molecular Analysis of Turkish β-Thalassemia Heterozygotes with Normal Hb A2 Levels von Öner, R., Birben, E., Acar, C., Öner, C., Kara, A., Gümrük, F., Gürgey, A., Altay, Ç.

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β-Thalassemia Intermedia in Turkey von ALTAY, Ç., GÜRGEY, A.

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Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis von ERICSON, Kim Göransdotter, FADEEL, Bengt, ANDERSSON, Mats, GUDMUNDSSON, Gudmundur H, GÜRGEY, Aytemiz, YALMAN, Nevin, JANKA, Gritta, NORDENSKJÖLD, Magnus, HENTER, Jan-Inge

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Prothrombin gene 20210 G‐A mutation in Turkish patients with thrombosis von Gürgey, Aytemiz, Hiçsönmez, Gönül, Parlak, Hülya, Balta, Günay, Çeliker, Alpay

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Molecular analysis of the Turkish form of deletion‐inversion (δβ)° thalassaemia von O¨NER, C., O¨NER, R., BALKAN, H., GU¨RGEY, A., YALC¸IN, A., AVCU, F., ALTAY, C¸.

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The molecular basis of β-thalassemia in Turkey von BASAK, A. N, ÖZCELIK, H, KIRDAR, B, ÖZER, A, TOLUN, A, AKSOY, M, AGAOGLU, L, RIDOLFI, F, ULUKUTLU, L, AKAR, N, GÜRGEY, A

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Parameters of iron deficiency in children with cyanotic congenital heart disease von Olcay, L, Ozer, S, Gürgey, A, Saraçlar, M, Ozme, S, Bilgiç, A, Ozkutlu, S, Celiker, A

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High dose intravenous methylprednisolone for Kassabach-Merritt syndrome von OZSOYLU, S, IRKEN, G, GURGEY, A

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Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family von Sözen, M., Karaaslan, Ç., Öner, R., Gümrük, F., Özdemir, M.A., Altay, C., Gürgey, A., Öner, C.

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