Sickle cell anemia basic (7 Ergebnisse)
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Anbieter: Salish Sea Books, Bellingham, WA, USASalish Sea Books
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Zustand: Fair. Fair-to-Good; Hardcover; Covers are still glossy, but with many light scratches to the front and back covers; Unblemished textblock edges; The endpapers and all text pages are bright and unmarked; The binding is tight with a straight spine; This book will be shipped in a sturdy cardboard box with foam padding; Med…ium-Large Format (Quatro, 9.75" - 10.75" tall); Dark blue covers with title in white lettering; 2016, Springer-Verlag Publishing; 450 pages; "Sickle Cell Anemia: From Basic Science to Clinical Practice," by Fernando Ferreira Costa & Nicola Conran.
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Gebunden. Zustand: New. KlappentextA sickle cell disease is a group of blood disorders that a person inherits from parents. They usually occur when the person inherits two abnormal copies of the hemoglobin gene. Sickle cell anemia is the most common type of sic.
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Anbieter: Revaluation Books, Exeter, Vereinigtes KönigreichRevaluation Books
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Hardcover. Zustand: Brand New. 205 pages. 11.00x8.50x0.67 inches. In Stock.
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Taschenbuch. Zustand: Neu. Sickle Cell Anemia | From Basic Science to Clinical Practice | Nicola Conran (u. a.) | Taschenbuch | xv | Englisch | 2018 | Springer International Publishing | EAN 9783319791531 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]sprin…ger[dot]com | Anbieter: preigu.
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Anbieter: AHA-BUCH GmbH, Einbeck, DeutschlandAHA-BUCH GmbH
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Buch. Zustand: Neu. Neuware - A sickle cell disease is a group of blood disorders that a person inherits from parents. They usually occur when the person inherits two abnormal copies of the hemoglobin gene. Sickle cell anemia is the most common type of sickle cell disease. It causes an abnormality in hemoglobin, the oxygen-carry…ing protein found in red blood cells. The problems due to sickle cell anemia begin to appear around 5 to 6 months of age. It leads to problems such as sickle cell crisis, swelling in hands and feet, stroke and bacterial infections. The care of people suffering from sickle cell anemia includes infection prevention with vaccination and antibiotics, folic acid supplementation and pain medication. A bone marrow transplant is also used in certain cases. This book consists of contributions made by international experts. It contains some path-breaking studies in sickle cell anemia. It will serve as a valuable source of reference for graduate and post graduate students.
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Anbieter: AHA-BUCH GmbH, Einbeck, DeutschlandAHA-BUCH GmbH
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Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not fully understood. A single mutation in the beta-globin gene incurs numerous molecular and cellular mechanisms that…contribute to the plethora of symptoms associated with the disease. Our knowledge regarding sickle cell disease mechanisms, while still not complete, has broadened considerably over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the disease's pathophysiology and use this information as a basis to discuss its manifestations in childhood and adulthood. Current therapies and prospects for the development of new approaches for the management of the disease are also covered.
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Anbieter: AHA-BUCH GmbH, Einbeck, DeutschlandAHA-BUCH GmbH
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Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not fully understood. A single mutation in the beta-globin gene incurs numerous molecular and cellular mechanisms that contrib…ute to the plethora of symptoms associated with the disease. Our knowledge regarding sickle cell disease mechanisms, while still not complete, has broadened considerably over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the disease's pathophysiology and use this information as a basis to discuss its manifestations in childhood and adulthood. Current therapies and prospects for the development of new approaches for the management of the disease are also covered.
