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Atlas of Inherited Metabolic Diseases 3E

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Atlas of Inherited Metabolic Diseases 3E
  • Forlagets pris kr. 1.849,95
  • Leveringstid 5-8 hverdage
  • Forventet levering 04-06-2018
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  1. Beskrivelse

    A new edition of this comprehensive source of practical and highly illustrated information covering the whole spectrum of metablic disease. 680 colour halftones and 160 line diagrams; 160 Line drawings, black and white; 680 Halftones, color; 680 Illustrations, color; 160 Illustrations... Læs mere

    Udgivelsesdato:
    30-12-2011
    Leveringstid:
    5-8 hverdage
    Bedømmelse:
    (0)
  2. Yderligere info
    Udgivelsesdato:
    30-12-2011
    Sprog:
    Engelsk
    ISBN13:
    9781444112252
    Sidetal:
    888
    Vægt:
    2654
    Højde:
    44
    Bredde:
    210
    Længde:
    276
    Mærkat:
    Bog, ukendt format
    Format:
    Ukendt
    Udgave:
    3rd New edition
    • Bibliotekernes beskrivelse

      In a field where even experts may find that years have elapsed since they last encountered a child with a given disorder, it is essential for the clinician to have a comprehensive source of practical and highly illustrated information covering the whole spectrum of metabolic disease to refer to. The third edition of this highly regarded book, authored by three of the foremost authorities in pediatric metabolic medicine, fulfils this need by providing an invaluable insight into the problems associated with metabolic diseases.The Atlas of Metabolic Disease is divided into sections of related disorders, such as disorders of amino acid metabolism, lipid storage disorders and mitochondrial diseases, with an introductory outline where appropriate summarizing the biochemical features and general management issues. Within sections each chapter deals with an individual disease, starting with a useful summary of major phenotypic expression and including clear and helpful biochemical pathways, identifying for the reader exactly where the defect is occurring.Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis.

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