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over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the;
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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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research and clinical focus Covering the genetic basis of the disease along with the most current work in gene editing, Sickle Cell Disease;
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; Chapter 1. The Essentials on Sickle Cell Anemia: Guidelines; Chapter 2. Seeking Guidance; Chapter 3. Clinical Trials and Sickle Cell Anemia; PART;
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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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. Callaghan has put together a comprehensive issue with clinical reviews written by top experts in the field. Articles are devoted to the following;
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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 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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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 (SCD) is a genetic disorder caused by an abnormality of hemoglobin. The disease is characterized by a chronic hemolytic;
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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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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 disease (SCD), an inherited hemolytic anemia, is associated with multiple acute and chronic complications such as painful;
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and will include articles on Blood Dyscriasis: Classification and Clinical Neurological Presentations, Imaging Manifestation of Anemia, CNS;
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medicine and will include articles on: RBC Transfusions: Conclusions from Clinical Trials and the Establishment of Evidence-based Guidelines for;
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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 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 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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Pain management is an essential part of clinical practice for all healthcare providers from trainees, physician assistants and nurse;
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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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, immunotherapies, personalized medicine, laboratory medicine, transfusion medicine, stem cell transplantation, and clinical treatment for all hematologic;
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; Congenital Hemolytic Anemia; Sickle Cell Disease; Thrombotic Microangiopathy; Unusual Anemias; and Transfusion Therapy.;
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sickle cell disease pain. It also contains chapters on specific client groups: children and the elderly.;
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