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    Online-Ressource
    Online-Ressource
    Berlin, Heidelberg : Springer-Verlag Berlin Heidelberg
    UID:
    gbv_1646604849
    Umfang: Online-Ressource (XVIII, 416p. 13 illus, digital)
    ISBN: 9783540289623
    Serie: SpringerLink
    Inhalt: This clinical reference provides concise information on the treatment and management of inherited metabolic diseases. World experts cover all commonalities of therapy giving practical advice and guidance. All established treatment protocols in this quickly developing area of medicine are clearly described, including follow-up protocols and monitoring. Alternative and experimental therapies are also described and evaluated. Numerous tables and figures allow rapid access to specific details. This book is invaluable to anyone dealing with patients with inherited metabolic diseases, pediatricians, internists, neurologists, and clinical geneticists.
    Anmerkung: Companion v. of: The physician's guide to the laboratory diagnosis of metabolic disease , Includes bibliographical references and indexes , Emergency Management of Metabolic Diseases; The Role of Communication in the Treatment of Inborn Metabolic Diseases; Disorders of Phenylalanine and Tetrahydrobiopterin Metabolism; Disorders of Neurotransmission; Disorders of GABA, Glycine, Serine, and Proline; Disorders of Tyrosine Degradation; Disorders of Histidine Metabolism; Disorders of Leucine Metabolism; Disorders of Valine-Isoleucine Metabolism; Various Organic Acidurias; Disorders of the .-Glutamyl Cycle; Disorders of Sulfur Amino Acid Metabolism; Inherited Hyperammonaemias; Disorders of Ornithine, Lysine, and Tryptophan , Defective Transcellular Transport of Amino AcidsDisorders of Mitochondrial Fatty Acid Oxidation and Ketone Body Metabolism; Disorders of Carbohydrate and Glycogen Metabolism; Disorders of Glucose Transport; Disorders of Glycerol Metabolism; The Mucopolysaccharidoses; Oligosaccharidoses and Related Disorders; Congenital Disorders of Glycosylation; Cystinosis; Other Storage Disorders; Inborn Errors of Purine and Pyrimidine Metabolism; Disorders of Creatine Metabolism; Peroxisomal Disorders; Hyperoxaluria; Mitochondrial Energy Metabolism; Genetic Dyslipoproteinemias , Disorders of Steroid Synthesis and MetabolismInborn Errors of Cholesterol Biosynthesis; The Porphyrias; Disorders of Bile Acid Synthesis; Disorders of Copper, Zinc, and Iron Metabolism; Leukotrienes; Hyperinsulinism of Infancy; Other Metabolic Disorders
    Weitere Ausg.: ISBN 9783540229544
    Weitere Ausg.: Buchausg. u.d.T. Physician's guide to the treatment and follow-up of metabolic diseases Berlin : Springer, 2006 ISBN 354022954X
    Weitere Ausg.: ISBN 9783540229544
    Sprache: Englisch
    Fachgebiete: Medizin
    RVK:
    Schlagwort(e): Stoffwechselkrankheit ; Angeborene Krankheit ; Therapie ; Stoffwechselkrankheit ; Angeborene Krankheit ; Therapie ; Stoffwechselkrankheit ; Angeborene Krankheit ; Therapie ; Aufsatzsammlung ; CD-ROM
    URL: Volltext  (lizenzpflichtig)
    URL: Cover
    Mehr zum Autor: Blau, Nenad 1946-
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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