Inborn Metabolic Diseases Diagnosis and Treatment / edited by John Fernandes, Jean-Marie Saudubray, Georges van den Berghe.

The diagnosis of metabolic diseases is facilitated by this clinical book. Each disease-related chapter begins with a detailed description of the patient and the delineating symptoms necessary for establishing the diagnosis and differential diagnosis. The figures illustrate the metabolic derangement...

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Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Fernandes, John (Editor), Saudubray, Jean-Marie (Editor), Berghe, Georges van den (Editor)
Format: eBook
Language:English
Published: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 1995.
Edition:2nd ed. 1995.
Series:Springer eBook Collection.
Subjects:
Online Access:Click to view e-book
Holy Cross Note:Loaded electronically.
Electronic access restricted to members of the Holy Cross Community.

MARC

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505 0 |a I Diagnosis and Treatment: General Principles -- 1 Clinical Approach to Inherited Metabolic Diseases -- 2 Diagnostic Procedures: Function Tests and Postmortem Protocol -- 3 Emergency Treatments -- 4 Psychosocial Care of the Child and Family -- II Carbohydrate Metabolism -- 5 Glycogen Storage Diseases -- 6 Disorders of Galactose Metabolism -- 7 Disorders of Fructose Metabolism -- 8 Disorders of Gluconeogenesis -- III Mitochondrial Energy Metabolism -- 9 The Pyruvate Dehydrogenase Complex and Tricarboxylic Acid Cycle -- 10 The Respiratory Chain -- 11 Disorders of Fatty Acid Oxidation -- IV Aminoacids -- 12 Hyperphenylalaninaemias -- 13 Tyrosine -- 14 Urea Cycle Disorders -- 15 Homocystinuria Due to Cystathionine ?-Synthase Deficiency and Related Disorders -- 16 Ornithine -- 17 Nonketotic Hyperglycinemia -- V Peptide Metabolism -- 18 Disorders of the Gamma Glutamyl Cycle -- 19 Disorders of Small Peptides -- VI Organic Acids -- 20 Branched-Chain Organic Acidurias -- 21 Ketolysis Defects -- 22 Glutaric Aciduria Type I and Related Cerebral Organic Acid Disorders -- VII Vitamin-Responsive Disorders -- 23 Biotin-Responsive Multiple Carboxylase Deficiency -- 24 Inherited Disorders of Cobalamin and Folate Absorption and Metabolism -- VIII Lipids -- 25 Dyslipidemias -- IX Nucleic Acids -- 26 Disorders of Purine and Pyrimidine Metabolism -- X Neurotransmitters -- 27 Disorders of Neurotransmitters -- XI Metals -- 28 Copper: Wilson and Menkes Diseases -- 29 Genetic Defects Related to Metals Other Than Copper -- XII Porphyrins and Herne -- 30 Porphyrias -- 31 Inborn Errors of Bile Acid Synthesis -- 32 Bilirubin -- XIII Membrane Transport -- 33 Alpha-l-Antitrypsin Deficiency -- 34 Transport Defects of Amino Acids at the Cell Membrane: Cystinuria, Hartnup Disease, and Lysinuric Protein Intolerance -- XIV Organelle Disorders: Lysosomes, Golgi and Pre-Golgi Systems, Peroxisomes -- 35 Sphingolipids -- 36 Mucopolysaccharides and Oligosaccharides -- 37 Cystinosis -- 38 Carbohydrate-Deficient Glycoprotein Syndromes -- 39 Peroxisomal Disorders -- 40 Oxalosis (Primary Hyperoxaluria) -- XV New Trends of Treatment -- 41 Liver Transplantation -- 42 Bone Marrow Transplantation -- 43 Somatic Gene Therapy. 
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