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Addressing Sickle Cell Disease

Sickle cell disease (SCD) is a genetic condition that affects approximately 100,000 people in the United States and millions more globally;

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The 2002 Official Patient's Sourcebook On Sickle Cell Anemia

to look for information covering virtually all topics related to sickle cell anemia, from the essentials to the most advanced areas;

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Sickle Cell Anemia

Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not;

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Sickle Cell Disease

Sickle cell disease (SCD) is a group of inherited blood disorders. Sickle cell anemia (SCA) is the most common form of SCD. It;

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Sickle Cell Disease in Clinical Practice

Sickle Cell Disease is the most common genetic disease world wide and in the UK. It has marked geographical variation in its distribution;

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Renaissance Of Sickle Cell Disease Research In The Genome Era

with sickle cell disease in the Genome Era. This book offers a comprehensive and timeless account of emerging concepts in clinical and basic;

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Sickle Cell Disease

any online entitlements included with the product. The first text to provide comprehensive coverage of sickle cell disease with both a;

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Sickle Cell Disease

Sickle cell disease (SCD) is a genetic disorder caused by an abnormality of hemoglobin. The disease is characterized by a chronic hemolytic;

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Benign Hematologic Disorders in Children, An Issue of Pediatric Clinics of North America

topics: Hemophilia; Sickle cell acute chest; Sickle cell drugs; Sickle cell gene therapy; Sickle cell menses and pain; Pediatric DVT; Atypical;

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Lee Has Yellow Eyes

Sickle Cell awareness at home and school... After raising my son who has sickle cell disease SS I was sure I was prepared for all of his;

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Sickle Cell Anemia

Sickle cell disease (SCD), an inherited hemolytic anemia, is associated with multiple acute and chronic complications such as painful;

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Sickle Cell Disease

Sickle cell hemoglobin (HbS) is the result of a single nucleotide change (GAG GTG) in the -globin gene, where valine replaces glutamic acid;

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Emerging Therapies Targeting the Pathophysiology of Sickle Cell Disease, An Issue of Hematology/Oncology Clinics

This issue of Hematology/Oncology Clinics, guest edited by Dr. Elliott Vichinsky, is devoted to Sickle Cell Disease, and focuses on;

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Sickle Cell and the Social Sciences

Sickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born;

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Sickle Cell and the Social Sciences

Sickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born;

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Jesus, Prophet of Islam

sickle cell disease pain. It also contains chapters on specific client groups: children and the elderly.;

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Jesus, Prophet of Islam

sickle cell disease pain. It also contains chapters on specific client groups: children and the elderly.;

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The Enculturated Gene

In the 1980s, a research team led by Parisian scientists identified several unique DNA sequences, or haplotypes, linked to sickle cell;

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Anemia, An Issue of Medical Clinics of North America

; Congenital Hemolytic Anemia; Sickle Cell Disease; Thrombotic Microangiopathy; Unusual Anemias; and Transfusion Therapy.;

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Management of Sickle Cell Disease in sub-Saharan Africa

Sickle cell disease (SCD) poses a major public health challenge in sub-Saharan Africa. Nigeria, being the most populous black nation in the;

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New Developments in Sickle Cell Disease Research

Sickle cell anaemia is an inherited blood disorder, characterised primarily by chronic anaemia and periodic episodes of pain and occurring;

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The Morpher

This book is about one womans spiritual and emotional awakening while living to die with SCA, sickle cell anemia disease. How she came to;

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Imaging of Neurologic Complications in Hematological Disorders

Complications of Hemorrhagic and Coagulation Disorders, Neurological and Head and Neck Manifestation of Sickle Cell Disease, Neuroimaging in Lymphoma;

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