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Thalassemia, An Issue of Hematology/Oncology Clinics of North America

Thalassemia is discussed comprehensively by the authors in this issue. Topics discussed include the population genetics and dynamimcs;

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Thalassemia

Thalassemia is one of the most common genetic disorders worldwide and presents major public health and social challenges in areas of high;

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Thalassemia, An Issue of Hematology/Oncology Clinics of North America

This issue of Hematology/Oncology Clinics, edited by Dr. Ali Taher, focuses on Thalassemia. Topics include, but are not limited to;

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Beta Thalassemia - A Data Analytics Perspective

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Coinheritance of Thalassemia Syndromes with Sickle Cell Disease

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Cooleys Anemia

Thanks to scientific advances, individuals with thalassemia-a group of genetic blood disorders which includes Cooley's Anemia - are now;

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Role of Hepcidin Hormone in Patients of ss-Thalassemia Major

, intermediate and minor forms of illness. The -thalassemias are the most important types of thalassemia because they are so common and usually produce;

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Iron Disorders, An Issue of Hematology/Oncology Clinics

Overload and its Management in Non-Transfusion-Dependent Thalassemia; Treatment of Iron Deficiency Anemia; and Iron Overload Assessment.;

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Can't Live Without It

haemoglobin: sickle-cell anaemia, pernicious anaemias, iron-deficiency anaemia, porphyries, haemoglobin E disease, alpha-thalassemia, beta-thalassemia;

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Bone Marrow Transplantation, An Issue of Hematology/Oncology Clinics of North America

); Hodgkin Lymphoma (HL); Severe Aplastic Anemia (SAA) and Paroxysmal Nocturnal Hemoglobinuria (PNH); Sickle Cell Anemia; Thalassemia; Benign;

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An Update on Pediatric Oncology and Hematology , An Issue of Hematology/Oncology Clinics of North America

aspects that most clinicians see on a regular basis-sickle cell disease, thalassemia, and hemophilia, and ITP.;

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Hematology in the Adolescent Female

thrombocytopenic purpura, as well as vitamin deficiencies due to pernicious anemia. Sickle cell disease, thalassemia and bone marrow failure disorders;

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Hematopoietic Stem Cells

adjustment of families of children who undergo HSCT; the immunogenetics of unrelated HSCT for thalassemia; HSCT for inflammatory bowel diseases; and;

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Pediatric Hematology , An Issue of Hematology/Oncology Clinics of North America

limited to, Rare Congenital Hemolytic Anemias, Sickle Cell, Thalassemia, Neutropenia and rare leukocyte disorders in children, Primary and;

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New Frontiers in Hematology

treatment of patients with blood disorders such as hematological malignancies, coagulopathies, sickle cell anemia, thalassemia, etc. This book;

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Advances in Medicine and Biology

microarchitecture. A summary of the involvement of miRNAs in different beta-thalassemia variants, their association in expression of various globin types;

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Fetal Hemoglobin

(e.g. I(2)-hemoglobinopathies like I(2)-thalassemia, sickle cell disease etc.). Early researchers in the field expected such patients to suffer;

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Advances in Biomolecular Medicine

, thalassemia, nutrition, cardiovascular, wound healing and endocrinology. This book is essential reading for academics, scientist, practitioners and;

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Disorders of Hemoglobin

biology, the erythrocyte membrane, nitric oxide biology, and hemolysis. Four sections deal with and thalassemia, sickle cell disease, and;

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Turning Blood Red

This book is the story of an inherited blood disease - Cooley's anemia or beta thalassemia. Cooley's anemia is a severe and potentially;

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A Closer Look at Polyadenylation

synthesis of one or more of the globin chains (thalassemia). The point mutation AATAAA to AACAAA of a human ss-globin gene detected in 1985 in DNA;

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Child Health in the Tropics

. Tuchinda, V. Suvatte and S. Tuchinda, Bodily growth in thalassemia ...43 L. Sinisterra, Ecological evaluation of human development: the case of the;

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Metal Ions in Biochemistry

such as iron in leukaemia, thalassemia and sickle cell anaemia, iodine in hypothyroidism and zinc, vanadium and chromium in glucose metabolism;

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Horizons in World Cardiovascular Research

high risk beta-thalassemia major patients for arrhythmias and sudden cardiac death. The authors also examine the coronary vasospasm as a;

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Human Gene Therapy

a new age in medical treatment. Modern medicine has had relatively little to offer children with disorders such as thalassemia and severe;

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Essential Metals in Medicine

is addressed in the context of thalassemia, its relationship to neurodegenerative diseases and also the risks connected with iron administration are;

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Hematology

for sickle cell disease and thalassemia, the evolution of cellular therapy, use of cells, transfusion medicine vs. protein therapy, gene;

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