Thalassemia

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Thalassemia

LE WE PMID CA

Thalassemia

2695

Thalassaemie

Anemia (Sickle cell)

Heart (Cardiomyopathy BASKET)

Heart failure (chronical)

Hemoglobin F

Histone deacetylase

Iron (Chelator)

Iron (Toxicology)

Thalassemia

1983 1	Thalassemic hemoglobinopathies. [6359893] Am J Pathol 113(3): 396-409 (1983)
2002 2	The hypercoagulable state in thalassemia. [11756150] Blood 99(1): 36-43 (2002)
1997 3	Iron-chelating therapy and the treatment of thalassemia. [9028304] Blood 89(3): 739-61 (1997)
1984 4	Advances in thalassemia research. [6200160] Blood 63(4): 738-58 (1984)
2008 5	Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders. [18413891] Haematologica 93(5): 741-52 (2008)
2005 6	Combined therapy with deferiprone and desferrioxamine in thalassemia major. [16219564] Haematologica 90(10): 1304-5 (2005)
2003 7	Comparative effects of deferiprone and deferoxamine on survival and cardiac disease in patients with thalassemia major: a retrospective analysis. [12745268] Haematologica 88(5): 489-96 (2003)
2003 8	Treatment of cardiac iron overload in thalassemia major. [12745264] Haematologica 88(5): 481-2 (2003)
2004 9	Thalassemia. [15561674] Hematology Am Soc Hematol Educ Program -(-): 14-34 (2004)
2010 10	Genetic correction of sickle cell anemia and beta-thalassemia: progress and new perspective. [20419277] ScientificWorldJournal 10(-): 644-54 (2010)
2010 11	The life of patients with thalassemia major. [20207838] Haematologica 95(3): 345-8 (2010)
2007 12	Heart disease in thalassemia intermedia: a review of the underlying pathophysiology. [17488690] Haematologica 92(5): 658-65 (2007)
2005 13	Genetic modifiers of beta-thalassemia. [15921380] Haematologica 90(5): 649-60 (2005)
2010 14	Update on iron chelators in thalassemia. [21239834] Hematology Am Soc Hematol Educ Program 2010(-): 451-5 (2010)
2010 15	Hematopoietic stem cell transplantation in thalassemia. [21239835] Hematology Am Soc Hematol Educ Program 2010(-): 456-62 (2010)
2009 16	Hb H disease: clinical course and disease modifiers. [20008179] Hematology Am Soc Hematol Educ Program -(-): 26-34 (2009)
2009 17	Alpha thalassemia major--new mutations, intrauterine management, and outcomes. [20008180] Hematology Am Soc Hematol Educ Program -(-): 35-41 (2009)
2010 18	Foetal haemoglobin inducers and thalassaemia: novel achievements. [20104272] Blood Transfus 8(1): 5-7 (2010)
2008 19	Histone deacetylase inhibitors and hemoglobin F induction in beta-thalassemia. [18617435] Int J Biochem Cell Biol 40(11): 2341-7 (2008)
2005 20	Physiology and pathophysiology of iron cardiomyopathy in thalassemia. [16339687] Ann N Y Acad Sci 1054(-): 386-95 (2005)
2009 21	Iron overload thalassemic cardiomyopathy: iron status assessment and mechanisms of mechanical and electrical disturbance due to iron toxicity. [19340344] Can J Cardiol 25(4): 213-8 (2009)
2010 22	Alpha-thalassaemia. [20507641] Orphanet J Rare Dis 5(-): 13 (2010)
2010 23	Beta-thalassemia. [20492708] Orphanet J Rare Dis 5(-): 11 (2010)
2010 24	Beta-thalassemia cardiomyopathy: history, present considerations, and future perspectives. [20484195] Circ Heart Fail 3(3): 451-8 (2010)
2008 25	The heart in transfusion dependent homozygous thalassaemia today--prediction, prevention and management. [18081719] Eur J Haematol 80(2): 93-106 (2008)
2010 26	Anemia, ineffective erythropoiesis, and hepcidin: interacting factors in abnormal iron metabolism leading to iron overload in beta-thalassemia. [21075282] Hematol Oncol Clin North Am 24(6): 1089-107 (2010)
PMC 27	The Correlation between Troponin and Ferritin Serum Levels in the Patients with Major Beta-Thalassemia. [24757621] Int Cardiovasc Res J 7(2):51-5 (2013)

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