Inborn Metabolic Diseases: Diagnosis and Treatment Saudubray, Jean-Marie? Berghe, Georges van den; Walter, John H. - gebunden oder broschiert
2012, ISBN: 9783642157196
Springer, Auflage: 2nd ed. 2012. Auflage: 2nd ed. 2012. Hardcover. 5 x 17,8 x 25,5 cm. In its revised Second Edition, this book offers new and updated chapters and references, and unique… Mehr…
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ISBN: 9783642157196
Now in its 5th edition, this is the standard text for identification and management of patients with inborn errors of metabolism. Updates include newly discovered disorders and a chapter … Mehr…
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ISBN: 364215719X
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2012, ISBN: 9783642157196
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2012, ISBN: 364215719X
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Inborn Metabolic Diseases: Diagnosis and Treatment Saudubray, Jean-Marie? Berghe, Georges van den; Walter, John H. - gebunden oder broschiert
2012, ISBN: 9783642157196
Springer, Auflage: 2nd ed. 2012. Auflage: 2nd ed. 2012. Hardcover. 5 x 17,8 x 25,5 cm. In its revised Second Edition, this book offers new and updated chapters and references, and unique… Mehr…
ISBN: 9783642157196
Now in its 5th edition, this is the standard text for identification and management of patients with inborn errors of metabolism. Updates include newly discovered disorders and a chapter … Mehr…
ISBN: 364215719X
Mit Markierungen mit Leuchtstift auf Seite 278. Davon abgesehen exzellentes TOP Exemplar. Unbekannter Einband 2, [PU: Springer, Berlin/Heidelberg/New York, NY]
2012, ISBN: 9783642157196
Springer, 2012-01-20. 5th ed. 2012. Hardcover. Used:Good., Springer, 2012-01-20, 0
2012, ISBN: 364215719X
[EAN: 9783642157196], [SC: 4.68], [PU: Springer], Most items will be dispatched the same or the next working day., Books
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Detailangaben zum Buch - Inborn Metabolic Diseases: Diagnosis and Treatment
EAN (ISBN-13): 9783642157196
ISBN (ISBN-10): 364215719X
Gebundene Ausgabe
Erscheinungsjahr: 2012
Herausgeber: Springer
656 Seiten
Gewicht: 1,573 kg
Sprache: Englisch
Buch in der Datenbank seit 2009-09-14T20:03:26+02:00 (Vienna)
Detailseite zuletzt geändert am 2023-08-23T12:04:14+02:00 (Vienna)
ISBN/EAN: 364215719X
ISBN - alternative Schreibweisen:
3-642-15719-X, 978-3-642-15719-6
Alternative Schreibweisen und verwandte Suchbegriffe:
Autor des Buches: van den berghe, george van den bergh, georges jean, john bergh, van den berg, georg walter, aubourg, marie
Titel des Buches: the diagnosis and treatment diseases
Daten vom Verlag:
Autor/in: Jean-Marie Saudubray; Georges van den Berghe; John H. Walter
Titel: Inborn Metabolic Diseases - Diagnosis and Treatment
Verlag: Springer; Springer Berlin
660 Seiten
Erscheinungsjahr: 2011-11-23
Berlin; Heidelberg; DE
Gedruckt / Hergestellt in Deutschland.
Gewicht: 1,633 kg
Sprache: Englisch
197,94 € (DE)
203,49 € (AT)
203,50 CHF (CH)
Not available, publisher indicates OP
BB; Book; Hardcover, Softcover / Medizin/Klinische Fächer; Pädiatrie; Verstehen; Medizin, Gesundheit; disorders of metabolism; inborn errors of metabolism; neonatal screening; metabolic diseases; newborn screening; inherited metabolic diseases; B; Medicine; Pediatrics; Human Genetics; Endocrinology; Neurology; Genetik, Medizin; Endokrinologie; Neurologie und klinische Neurophysiologie; BB; BC; EA; BB
Part I: Diagnosis and Treatment: General Principles: Classification and clinical Approach to Inherited Metabolic Diseases in Pediatrics.- Clinical approach to Inherited Metabolic Diseases in Adulthood.- Newborn Screening for Inborn Errors of Metabolism.- Diagnostic Procedures and Postmortem Protocol.- Emergency Treatments.- Part II: Disorders of Carbohydrate Metabolism: Glycogen-Storage Diseases and Related Disorders.- Disorders of Galactose Metabolism.- Disorders of the Pentose Phosphate Pathway.- Disorders of Fructose Metabolism.- Persistent Hyperinsulinemic Hypoglycemia.- Disorders of Glucose Transport.- Part III: Disorders of Mitochondrial Energy Metabolism: Disorders of Pyruvate Metabolism and the Tricarboxylic Acid Cycle.- Disorders of Mitochondrial Fatty Acid Oxidation and Related Metabolic Pathways.- Disorders of Ketogenesis and Ketolysis.- Defects of the Respiratory Chain.- Creatine Deficiency Syndromes.- Part IV: Disorders of Amino Acid Metabolism and Transport: Hyperphenylalaninaemias.- Disorders of Tyrosine Metabolism.- Branched-Chain Organic Acidurias/Acidemias.- Disorders of the Urea Cycle and Related Enzymes.- Disorders of Sulfur Amino Acid Metabolism.- Disorders of Ornithine Metabolism.- Cerebral Organic Acid Disorders and other Disorders of Lysine Catabolism.- Nonketotic Hyperglycinemia (Glycine Encephalopathy).- Disorders of Proline and Serine Metabolism.- Transport Defects of Amino Acids at the Cell Membrane.- Part V : Vitamin-Responsive Disorders: Biotin-Responsive Multiple Carboxylase Deficiency.- Disorders of Cobalamin and Folate Transport and Metabolism.- Part VI: Neurotransmitter and Small Peptide Disorders: Disorders of Neurotransmission.- Disorders in the Metabolism of Glutathione and Imidazole Dipeptides.- Trimethylaminuria and Dimethylglycine Dehydrogenase Deficiency.- Part VII: Disorders of Lipid and Bile Acid Metabolism: Dyslipidemias.- Disorders of Cholesterol Synthesis.- Disorders of Bile Acid Synthesis.- Part VIII: Disorders of Nucleic Acid and Heme Metabolism: Disorders of Purine and Pyrimidine Metabolism.- Disorders of Heme Biosynthesis.- Part IX: Disorders of Metal Transport: Disorders in the Transport of Copper, Zinc and Magnesium.- Part X: Organelle-Related Disorders: Lysosomes, Peroxysomes, and Golgi and Pre-Golgi Systems: Disorders of Sphingolipid Metabolism and Ceroid lipofuscinosis.- Pompe Disease, Mucopolysaccharidoses, and Oligosacharidoses.- Peroxisomal Disorders.- Congenital Disorders of Glycosylation.- Cystinosis.Weitere, andere Bücher, die diesem Buch sehr ähnlich sein könnten:
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