REFERENCES
- Galacteros F, Girodon E, M’Rad A, . Hb Taybe (α38 or 39 THR deleted): an α-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous. CR Acad Sci III. 1994;317(5):437–444.
- Oron-Karni V, Filon D, Shifrin Y, . Diversity of α-globin mutations and clinical presentation of α-thalassemia in Israel. Am J Hematol. 2000;65(3):196–203.
- Pobedimskaya DD, Molchanova TP, Streichman S, Huisman THJ. Compound heterozygosity for two α-globin gene defects, Hb Taybe (α1; 38 or 39 minus Thr) and a poly A mutation (α2; AATAAA→AATAAG), results in a severe hemolytic anemia. Am J Hematol. 1994;47(3):198–202.
- Ben-Bassat I, Simjanovska L, Jaber L, Efremov GD. Hb Taybe: description of genetics and laboratory findings in an Israeli Arab family. Hemoglobin. 1998;22(2):161–166.
- Arnon S, Tamary H, Dgany O, . Hydrops fetalis associated with homozygosity for Hemoglobin Taybe (α38/39 THR deletion) in newborn triplets. Am J Hematol. 2004;76(3):263–266.
- Douna V, Liapi D, Kampourakis D, . First observation of Hb Taybe [codons 38/39 (–ACC) Thr→0 (α1)] in Greece: clinical and hematological findings in patients with co-inherited α+-thalassemia mutations. Hemoglobin. 2008;32(4):371–378.
- Paglietti ME, Sollaino MC, Loi D, Barella S, Desogus MF, Galanello R. First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child. Hemoglobin. 2012;36(3):299–304.
- Taher A, Isma’eel H, Mehio G, . Prevalence of thromboembolic events among 8,860 patients with thalassaemia major and intermedia in the Mediterranean area and Iran. Thromb Haemost. 2006;96(4):488–491.
- Kim BJ, Park KW, Koh SB, . Stroke induced by splenectomy in Hemoglobin Madrid: autopsy clues to the underlying mechanism. Blood Coagul Fibrinol. 2005;16(2):141–144.
- Thuret I, Bardakdjian J, Badens C, . Priapism following splenectomy in an unstable hemoglobin: Hemoglobin Olmsted β141(H19)Leu→Arg. Am J Hematol. 1996;51(2):133–136.
- Gyan E, Darre S, Jude B, . Acute priapism in a patient with unstable Hemoglobin Perth and Factor V Leiden under effective oral anticoagulant therapy. Hematol J. 2001;2(3):210–211.
- Andrieu V, Dumonceau O, Grange MJ. Priapism in a patient with unstable hemoglobin: Hemoglobin Köln. Am J Hematol. 2003;74(1):73–74.
- Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood. 1996;88(10):3698–3703.
- Dahlback B. Advances in understanding pathogenic mechanisms of thrombophilic disorders. Blood. 2008;112(1):19–27.
- Casas JP, Hingorani AD, Bautista LE, Sharma P. Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch Neurol. 2004;61(11):1652–1661.
- Crary SE, Buchanan GR. Vascular complications after splenectomy for hematologic disorders. Blood. 2009;114(14):2861–2868.