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Blood, ISSN 0006-4971, 10/2018, Volume 132, Issue 17, pp. 1781 - 1791
Journal Article
American Journal of Hematology, ISSN 0361-8609, 08/2019, Volume 94, Issue 8, pp. E207 - E209
Journal Article
BLOOD, ISSN 0006-4971, 10/2018, Volume 132, Issue 17, pp. 1781 - 1791
The complex pathophysiology in beta-thalassemia can translate to multiple morbidities that affect every organ system. Improved survival due to advances in... 
HEPATOCELLULAR-CARCINOMA | TRANSFUSION-DEPENDENT THALASSEMIA | PULMONARY ARTERIAL-HYPERTENSION | CARDIOVASCULAR MAGNETIC-RESONANCE | C VIRUS-INFECTION | RANDOMIZED CONTROLLED-TRIAL | MYOCARDIAL IRON | LIVER IRON CONCENTRATION | HEMATOLOGY | LONG-TERM TREATMENT | HEPATITIS-C
Journal Article
2008, 2nd revised edition., ISBN 9789963623709
Written by some of the world's leading authorities on haemoglobin disorders, this second revised edition of Guidelines for the Clinical Management of... 
therapy | Thalassemia
Web Resource
Cancer, ISSN 0008-543X, 05/2017, Volume 123, Issue 6, pp. 1073 - 1073
Journal Article
Drugs, ISSN 0012-6667, 10/2014, Volume 74, Issue 15, pp. 1719 - 1719
Despite their transfusion-independence, nontransfusion-dependent thalassemia (NTDT) patients experience a variety of serious clinical complications that... 
Journal Article
Annals of Hematology, ISSN 0939-5555, 4/2019, Volume 98, Issue 4, pp. 833 - 840
Beta-thalassemia can present with a wide spectrum of phenotypes determined by the coinheritance of α-thalassemia, hereditary persistence of fetal hemoglobin,... 
Phenotype | Transfusion | Medicine & Public Health | Hematology | Oncology | Thalassemia | Single nucleotide polymorphisms | Fetal hemoglobin | MODIFIERS | HEMATOLOGY | INTERMEDIA | Codon | Gene mutations | Genes | Glycosylated hemoglobin | Genetic research | Genetic aspects
Journal Article
Seminars in Hematology, ISSN 0037-1963, 10/2015, Volume 52, Issue 4, pp. 259 - 260
Journal Article
Internal and Emergency Medicine, ISSN 1828-0447, 8/2018, Volume 13, Issue 5, pp. 709 - 712
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s11739-017-1764-z 
Medicine & Public Health | Internal Medicine | MEDICINE, GENERAL & INTERNAL | CRISIS | PATIENT | SICKLE-CELL-DISEASE | HEMOGLOBIN-C-DISEASE | Thrombocytopenic purpura | Hemoglobin | Thrombotic thrombocytopenic purpura | Blood platelets | Purpura | Thrombosis
Journal Article
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 2007, Volume 2007, Issue 1, pp. 74 - 78
Coagulation abnormalities are frequently reported in hemolytic anemias (HA). Several pathophysiologic mechanisms are common to different HA. In this review... 
Humans | Anemia, Hemolytic - physiopathology | Anemia, Hemolytic - therapy | Blood Coagulation
Journal Article
Clinical Therapeutics, ISSN 0149-2918, 2009, Volume 31, pp. S169 - S170
Journal Article
Clinical Therapeutics, ISSN 0149-2918, 2009, Volume 31, Issue 3, pp. S169 - S170
Journal Article
Clinical Therapeutics, ISSN 0149-2918, 01/2009, Volume 31, pp. S169 - S170
Journal Article
Clinical Therapeutics, ISSN 0149-2918, 01/2009, Volume 31, p. S169
Journal Article
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