The Xmn1 polymorphic site 5′ to the Gγ gene and its correlation to the Gγ:Aγ ratio, age at first blood transfusion and clinical features in β-Thalassemia patients from Western Iran
暂无分享,去创建一个
[1] B. Bain. Disorders of Hemoglobin: Genetics, Pathophysiology and Clinical Management , 2011 .
[2] P. Landais,et al. Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia , 2007, Transfusion.
[3] P. Vicari,et al. XmnI polymorphism is associated with fetal hemoglobin levels in hypoplastic syndromes. , 2006, Sao Paulo medical journal = Revista paulista de medicina.
[4] M. Sutton,et al. Pharmacological Induction of Fetal Hemoglobin: Why Haven't We Been More Successful in Thalassemia? , 2005, Annals of the New York Academy of Sciences.
[5] A. Bahador,et al. Management of thalassemia major by partial splenectomy , 1994, Pediatric Surgery International.
[6] E. Rachmilewitz,et al. MEDICAL PROGRESS : β-thalassemia , 2005 .
[7] R. Ware,et al. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. , 2004, Blood.
[8] P. Vossough,et al. Hydroxyurea in the treatment of major β-thalassemia and importance of genetic screening , 2004, Annals of Hematology.
[9] Z. Rahimi,et al. β‐Globin gene cluster haplotypes in sickle cell patients from southwest Iran , 2003, American journal of hematology.
[10] S. Thein,et al. Evidence of genetic interaction between the beta-globin complex and chromosome 8q in the expression of fetal hemoglobin. , 2002, American journal of human genetics.
[11] H. Yarmohammadi,et al. β-THALASSEMIA INTERMEDIA FROM SOUTHERN IRAN: IVS-II-1 (G→A) IS THE PREVALENT THALASSEMIA INTERMEDIA ALLELE , 2002, Hemoglobin.
[12] D. Mohanty,et al. Molecular pathogenesis and clinical variability of β‐thalassemia syndromes among Indians , 2001 .
[13] U. Dasgupta,et al. Variable severity of β-thalassemia patients of Eastern India: effect of α-thalassemia and XmnI polymorphism , 2001, Clinical and Experimental Medicine.
[14] Y. Saunthararajah,et al. Advances in experimental treatment of β-thalassaemia , 2001 .
[15] F. Pourfarzad,et al. THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION , 2001, Hemoglobin.
[16] Y. Saunthararajah,et al. Advances in experimental treatment of beta-thalassaemia. , 2001, Expert opinion on investigational drugs.
[17] E. Rachmilewitz,et al. New trends in the treatment of -thalassemia , 2000 .
[18] E. Rachmilewitz,et al. New trends in the treatment of b-thalassemia , 2000 .
[19] E. Vichinsky,et al. Hydroxyurea and sodium phenylbutyrate therapy in thalassemia intermedia , 1999, American journal of hematology.
[20] T. Spector,et al. A candidate gene study of F cell levels in sibling pairs using a joint linkage and association analysis. , 1999 .
[21] D. Mohanty,et al. Variable clinical severity of Hb E beta-thalassemia among Indians. , 1999, The Journal of the Association of Physicians of India.
[22] Prescott,et al. High prevalence of low bone mass in thalassaemia major , 1998, British journal of haematology.
[23] E. Bakker. Methods in Molecular Medicine: Molecular Diagnosis of Genetic Diseases , 1997 .
[24] F. Costa,et al. Successful use of hydroxyurea in beta-thalassemia major. , 1997, The New England journal of medicine.
[25] G. Brittenham,et al. Iron-chelating therapy and the treatment of thalassemia. , 1997, Blood.
[26] H. Bard,et al. Association of -158(C → T) (XmnI) DNA Polymorphism inGγ-Globin Promoter with Delayed Switchover from Fetal to Adult Hemoglobin Synthesis , 1997, Pediatric Research.
[27] A. Schechter,et al. Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease. , 1996, Blood.
[28] J. Old. Hemoglobinopathies : community clues to mutation detection. , 1996, Methods in molecular medicine.
[29] F. Barton,et al. Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea. , 1995, Controlled clinical trials.
[30] M L Terrin,et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. , 1995, The New England journal of medicine.
[31] M. Vidaud,et al. A comprehensive scanning method for rapid detection of β‐globin gene mutations and polymorphisms , 1992, Human mutation.
[32] E. Rappaport,et al. The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression. , 1991, Hemoglobin.
[33] T. Huisman,et al. DNA sequence variation associated with elevated fetal G gamma globin production. , 1985, Blood.
[34] R. Schneider. Differentiation of electrophoretically similar hemoglobins--such as S, D, G, and P; or A2, C, E, and O--by electrophoresis of the globin chains. , 1974, Clinical chemistry.
[35] J. Clegg,et al. An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore) , 1965, Nature.