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  • 1
    Online Resource
    Online Resource
    London :IntechOpen,
    UID:
    almafu_9961356342702883
    Format: 1 online resource (242 pages)
    ISBN: 1-83768-400-6
    Content: The thalassemia syndromes are a diverse group of hereditary anemias caused by decreased or absent production of one type of globin chain. Genetic counseling, prenatal diagnosis, and newborn screening are all issues of importance in these inherited disorders. This book provides a comprehensive overview of thalassemia, including information on its mechanisms and treatment modalities. Chapters elucidate the mechanism of disordered synthesis of hemoglobin in thalassemia and present recent studies of the genetic mechanisms that underlie this abnormal biosynthetic process.
    Note: 1. Overview of Beta-Thalassemia -- 2. Effects of Beta-Thalassemia on COVID-19 Outcomes -- 3. Newborn Screening and Thalassaemia Syndrome -- 4. The Key Genetic Determinants Behind the Phenotypic Heterogeneity of HbE/β-thalassemia Patients and the Probable Management Strategy -- 5. Interaction of Thalassemia and Hb Variants in Southeast Asia: Genotype-Phenotype Relationship -- 6. The Thalassemia Syndromes: New Insights -- 7. Optimizing Blood Transfusion Service Delivery across the West African Sub-Region -- 8. Clinical Effects and Possible Mechanisms of Transfusion-Related Immunomodulation -- 9. Personnel for Blood Transfusion Services in Nigeria: A Multicenter Cooperative Study.
    Additional Edition: ISBN 1-83768-399-9
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    b3kat_BV049773358
    Format: 1 Online-Ressource , Illustrationen, Diagramme
    ISBN: 9781837684014 , 9781837684007
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-1-83768-399-4
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    UID:
    gbv_1885776330
    Format: 1 Online-Ressource (242 p.)
    ISBN: 9781837684007 , 9781837683994 , 9781837684014
    Content: The thalassemia syndromes are a diverse group of hereditary anemias caused by decreased or absent production of one type of globin chain. Genetic counseling, prenatal diagnosis, and newborn screening are all issues of importance in these inherited disorders. This book provides a comprehensive overview of thalassemia, including information on its mechanisms and treatment modalities. Chapters elucidate the mechanism of disordered synthesis of hemoglobin in thalassemia and present recent studies of the genetic mechanisms that underlie this abnormal biosynthetic process
    Note: English
    Additional Edition: ISBN 9781837683994
    Additional Edition: Erscheint auch als Print Thalassemia Syndromes - New Insights and Transfusion Modalities ISBN 9781837683994
    Language: Undetermined
    Library Location Call Number Volume/Issue/Year Availability
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