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Author:
Publisher: U.S. Government Printing Office
ISBN:
Category : Medical
Languages : en
Pages : 22
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Book Description
Author:
Publisher: U.S. Government Printing Office
ISBN:
Category : Medical
Languages : en
Pages : 22
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Book Description
Author: Mark T. Gladwin
Publisher: McGraw Hill Professional
ISBN: 1260458601
Category : Medical
Languages : en
Pages : 715
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Book Description
The most comprehensive, current sickle cell disease resource—for both clinicians and researchers A Doody's Core Title for 2023! The first and only resource of its kind, Sickle Cell Disease examines this blood disorder through both clinical and research lenses. More than 80 dedicated experts in the field present their combined clinical knowledge of basic mechanisms, screening, diagnosis, management, and treatment of myriad complex complications of a single base point mutation in the human genome. Case studies with “How I Treat” authoritative insights provide overviews of common and rare complications, and Key Facts offer at-a-glance high-yield information. Filled with clinical photos, illustrations, numerous original diagrams, and with free updates available online, this unmatched resource covers: Mechanisms of sickle cell disease Historic and current research approaches The latest work in gene therapy and editing Guidelines for patient care, diagnosis, unique cases, and therapies Rare and common complications, including domestic and internationally relevant topics Psychosocial and supportive care The newest standards of therapy and future treatment options in children and adults Cardiopulmonary complications
Author: Samir K. Ballas
Publisher: Lippincott Williams & Wilkins
ISBN: 1496331834
Category : Medical
Languages : en
Pages : 1004
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Book Description
Sickle Cell Pain is a panoramic, in-depth exploration of every scientific, human, and social dimension of this cruel disease. This comprehensive, definitive work is unique in that it is the only book devoted to sickle cell pain, as opposed to general aspects of the disease. The 752-page book links sickle cell pain to basic, clinical, and translational research, addressing various aspects of sickle pain from molecular biology to the psychosocial aspects of the disease. Supplemented with patient narratives, case studies, and visual art, Sickle Cell Pain’s scientific rigor extends through its discussion of analgesic pharmacology, including abuse-deterrent formulations. The book also addresses in great detail inequities in access to care, stereotyping and stigmatization of patients, the implications of rapidly evolving models of care, and recent legislation and litigation and their consequences.
Author: Jeanne A. Smith
Publisher: DIANE Publishing
ISBN: 078814703X
Category :
Languages : en
Pages : 110
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Book Description
Developed by a private-sector panel of health care experts and a consumer representative, this clinical practice guideline sets forth a comprehensive program for identifying, diagnosing, and treating newborns and infants with sickle cell disease and recommends education and counseling strategies for their parents. Addresses neonatal screening and provides specific recommendations on the newborn population to be screened, laboratory methods for screening and diagnosing the disease, and medical management of patients. Includes tables, glossary, references, and sources for patient education materials.
Author: Chaim Hershko
Publisher: Taylor & Francis US
ISBN: 9780306467851
Category : Medical
Languages : en
Pages : 290
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Book Description
Within the last few years, iron research has yielded exciting new insights into the understanding of normal iron homeostasis. Such development, and the evolution of improved strategies of Iron Chelating Therapy require better understanding of the pathophysiology of iron toxicity and the mechanism of action of iron chelating drugs. The timeliness of the present volume is underlined by several significant developments in recent years. New insights have been gained into the molecular basis of aberrant iron handling in hereditary disorders and the pathophysiology of iron overload. This volume highlights the impact of long term Iron Celating Therapy using deferoxamine or the new, but controversial oral iron chelator deferiprone based on experience gained by multicenter trails, with special emphasis on survival, morbidity and drug toxicity; it reviews the development of the new and improved orally effective chelators suitable for clinical use in the near future and examines novel strategies of iron chelating treatment for the control of cell proliferation in malignant disease or malaria.
Author:
Publisher:
ISBN:
Category : Sickle cell anemia
Languages : en
Pages : 60
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Book Description
481 entries to publications of investigators active in the programs of 15 sickle centers in the United States. Citations arranged under 9 topics, e.g., Hemoglobin, Flow studies, and Psychosocial. Entry gives bibliographical information. No index.
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 122
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Book Description
Author: United States. Sickle Cell Disease Guideline Panel
Publisher:
ISBN:
Category : Anemia in children
Languages : en
Pages : 116
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Book Description
Author: Paul D. O'Malley
Publisher: Nova Publishers
ISBN: 9781594547928
Category : Sickle cell anemia
Languages : en
Pages : 266
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Book Description
Author: Miriam Bloom
Publisher: Univ. Press of Mississippi
ISBN: 1604737573
Category : Health & Fitness
Languages : en
Pages : 137
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Book Description
Although more is known about sickle cell disease than about any other inherited disease, no cure for it exists. In America alone, about one in 375 who are of African ancestry is born with sickle cell disease. A smaller number of Americans descended from families from the Mediterranean area, the Middle East, and India also are affected. In addition, about eight percent of black Americans who do not suffer from the disease itself carry the gene for it that can be transmitted to their children. Sickle cell disease is of enormous biological, social, and historic importance. It was first described in medical literature almost a century ago. Improvements during the past two decades in our understanding of the disease and in medical care are permitting those afflicted to live longer, more comfortable and more productive lives. This book was written for all who are interested in this disease--those who have it, their families, the carriers of the sickle cell gene, teachers, and those who wish to update their information about it. This overview of sickle cell disease explains what it is and how it is inherited, as well as the relationship between the sickle cell gene and its geographic origins, the way the gene has been spread throughout history, and the effect of sickle cell hemoglobin on red blood cells that carry it. Understanding Sickle Cell Disease describes the variety of symptoms in both children and adults and details the emotional aspects of the disease. Of particular interest is a chapter on the care, especially the home care, of those who are affected. This book explains how it is possible today for couples carrying the genes to raise families free of the disease. Although there is no known cure for sickle cell disease, there is little doubt that one will ultimately be devised. This volume surveys current research efforts and the promise they hold.
