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African Americans --- Sickle cell anemia --- Sickle cell anemia --- Diseases. --- Social aspects --- History
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Immunology. Immunopathology --- Gastroenterology --- Medical microbiology, virology, parasitology --- Sickle cell anemia --- Hepatitis --- man --- Sickle cell anemia. --- Hepatitis. --- man. --- Man.
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Sociology of health --- Pathological haematology --- Ethnology. Cultural anthropology --- Africa --- Sickle cell anemia --- Sickle cell anemia. --- Anemia, Sickle Cell. --- Health Services, Indigenous
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Hemoglobinopathy --- Sickle cell anemia --- Anemia, Sickle cell --- Hemoglobinopathies --- Congresses. --- Congresses. --- Congresses. --- Congresses.
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This book addresses a wide range of clinically relevant topics and issues in sickle cell disease. This is written by experts in their own field offering a robust, engaging discussion about the presentations and mechanisms of actions in the multiple complications associated with sickle cell disease. This first of the series addresses pain, which is considered the hallmark of sickle cell presentation. It looks at the basic mechanism of pain in sickle cell disease. A more detailed review of precision medicine gives a clear well laid out presentation that is incisive and yet gives in-depth detail relevant to both the clinician and the researcher in the basic laboratory. The same pattern is shown in the discussion on respiratory, cardiac and neurological complications. The 14 chapters also include an overview of sickle cell disease especially in the paediatric age. The content is organized into well-designed broad sections on overview regarding diagnosis including point of care and the role of digital apps in patient management. A key aspect of the book is the opportunity it affords expert physicians to express well-reasoned opinions regarding complex issues in sickle cell disease. The readership would find that it provides a well-described, concise and immediate applicable answers to complex questions. This is highly recommended for scientists and clinicians alike.
Sickle cell anemia. --- Drepanocytic anemia --- Meniscocytosis --- Sickle cell disease --- Blood hyperviscosity syndrome --- Hemoglobinopathy --- Hemolytic anemia --- Medicine --- Hematology --- Hematopathology --- Health Sciences
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Pathological haematology --- Sickle cell anemia --- Anemia, Sickle Cell --- ANEMIA --- Congresses. --- congresses. --- SICKLE CELL --- Anemia --- Anemia, sickle cell --- Sickle cell --- Congresses --- ANEMIA, SICKLE CELL --- CONGRESSES
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Sickle cell anemia --- Antineoplastic agents --- Urea --- Diabetes Mellitus, Type 1 --- Child. --- Evidence-Based Medicine --- Outcome Assessment, Health Care. --- Patient Education as Topic --- Treatment --- Therapeutic use --- Derivatives --- Therapeutic use --- prevention & control. --- methods. --- methods.
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This book provides a comprehensive, state-of-the art review of hematopoietic stem cell transplantation (HSCT) for sickle cell disease (SCD). The book reviews new data about risk prediction for severe SCD, outlines the unique challenges of HSCT for patients with SCD, profiles the supportive care guidelines for patients who are undergoing HSCT, highlights our current understanding of the best transfusion support for SCD patients prior to, during and after HSCT, and provides new perspectives about the ethics of HSCT for pediatric patients with SCD. Published in the last few years, several landmark phase III trials that utilize matched unrelated and haploidentical donors for HSCT in SCD patients are also placed in context with respect to current management. Written by experts in the field, Sickle Cell Disease and Hematopoietic Stem Cell Transplantation is a valuable resource for physicians and researchers dealing with and interested in this challenging, yet exciting, curative therapy for sickle cell disease, that will help guide patient management and stimulate investigative efforts. .
Medicine. --- Hematology. --- Medicine & Public Health. --- Haematology --- Clinical sciences --- Medical profession --- Sickle cell anemia --- Hematopoietic stem cells --- Treatment. --- Transplantation. --- Drepanocytic anemia --- Meniscocytosis --- Sickle cell disease --- Blood hyperviscosity syndrome --- Hemoglobinopathy --- Hemolytic anemia --- Internal medicine --- Blood --- Diseases
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