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This edition was published in Germany, under German copyright. The ISBN listed is for the current edition. "In addition to better information about the classic lipid thesaurismoses Niemann-Pick disease, Gaucher's disease and Tay-Sachs disease, the number of hereditary lipid storage diseases has increased considerably through the recognition of new syndromes such as metachromatic leukodystrophy, Fabry's disease, Refsum's disease (heredopathia atactica polyneuritisformis), a-[Beta]-lipoproteinemia, and Tangier disease. In accordance with our interpretation of the term lipidoses as hereditary disorders of lipid metabolism, a review of secondary hyperlipidemias has not been attempted here." [Preface] Part I, Lipids, contains the following topics: The Chemistry of Mammalian Lipids (Stoffel); Biochemistry of Triglycerides (Shapiro); Biochemistry of Steroids (Kritchevsky); Biochemistry of Phosphatides (Rossiter); Biochemistry of Sphingosine Containing Lipids (Burton); Lipoproteins (Cornwell); and Methods for Separation and Determination of Lipids (Wagener). Part II, Lipidoses, contains Gangliosidoses (the Editor, Kahlke); Gaucher's Disease (the Editor, Kahlke), Niemann-Pick Disease (the Editor, Kahlke); Metachromatic Leucodystrophy (Kahlke); Angiokeratoma Corporis Diffusum (Fabry's Disease) (Kahlke); Heredopathia Atactica Polyneueritisformis (Refsum's Disease) (Kahlke); A-[Beta]-Lipoproteinemia (Kahlke); Tangier Disease (Kahlke); Essential Hypercholesterolemia (the Editor, et al.); Essential Hyperlipemia (Kinsell, et al.); and Genetic Aspects of Lipidoses (Fuhrmann). 622 pages, with tables, figures, plates, and 2 Indexes; plus xiv pages Preface, [List of] Contributors, and Contents; References at the end of each paper. DJ is chipped, torn, and shows color loss; boards are clean and sound; name of prior owner inked on rfEP; text is clean and strong.
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