Verlag: Cambridge University Press, 2002
ISBN 10: 0521890764 ISBN 13: 9780521890762
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Verlag: Cambridge University Press, 2002
ISBN 10: 0521890764 ISBN 13: 9780521890762
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Verlag: Cambridge University Press, 1996
ISBN 10: 052148524X ISBN 13: 9780521485241
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Verlag: Cambridge University Press, 1996
ISBN 10: 052148524X ISBN 13: 9780521485241
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Verlag: Cambridge University Press, 2002
ISBN 10: 0521890764 ISBN 13: 9780521890762
Sprache: Englisch
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Verlag: Cambridge University Press, 2002
ISBN 10: 0521890764 ISBN 13: 9780521890762
Sprache: Englisch
Anbieter: Better World Books Ltd, Dunfermline, Vereinigtes Königreich
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In den WarenkorbZustand: Very Good. 2nd. Ships from the UK. Former library book; may include library markings. Used book that is in excellent condition. May show signs of wear or have minor defects.
Verlag: Cambridge University Press, 1996
ISBN 10: 052148524X ISBN 13: 9780521485241
Sprache: Englisch
Anbieter: Better World Books Ltd, Dunfermline, Vereinigtes Königreich
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
Anbieter: Better World Books, Mishawaka, IN, USA
Zustand: Good. Former library book; may include library markings. Used book that is in clean, average condition without any missing pages.
Verlag: Cambridge University Press, 2006
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
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Verlag: Cambridge University Press, 2002
ISBN 10: 0521890764 ISBN 13: 9780521890762
Sprache: Englisch
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Verlag: Cambridge University Press, 2006
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Verlag: Cambridge University Press, 2006
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Verlag: Cambridge University Press, 1996
ISBN 10: 0521480647 ISBN 13: 9780521480642
Sprache: Englisch
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Verlag: Cambridge University Press CUP, 2006
ISBN 10: 0521614996 ISBN 13: 9780521614993
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Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
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Paperback. Zustand: new. Paperback. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis. The book is organized into chapters according to the most prominent presenting problem of patients with inherited metabolic diseases: neurologic, hepatic, cardiac, metabolic acidosis, dysmorphism, and acute catastrophic illness in the newborn. It also includes chapters on general principles, laboratory investigation, neonatal screening, and the principles of treatment. This new edition includes much greater depth on mitochondrial disease and congenital disorders of glycosylation. The chapters on neurological syndrome and newborn screening are greatly expanded, as are those on laboratory investigation and treatment, to take account of the very latest technological developments. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. To help make the correct diagnosis, the book is organized according to the clinical symptoms presenting in these patients. This new edition includes much new and up-dated material. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
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In den WarenkorbPaperback. Zustand: new. Paperback. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis. The book is organized into chapters according to the most prominent presenting problem of patients with inherited metabolic diseases: neurologic, hepatic, cardiac, metabolic acidosis, dysmorphism, and acute catastrophic illness in the newborn. It also includes chapters on general principles, laboratory investigation, neonatal screening, and the principles of treatment. This new edition includes much greater depth on mitochondrial disease and congenital disorders of glycosylation. The chapters on neurological syndrome and newborn screening are greatly expanded, as are those on laboratory investigation and treatment, to take account of the very latest technological developments. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. To help make the correct diagnosis, the book is organized according to the clinical symptoms presenting in these patients. This new edition includes much new and up-dated material. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
Anbieter: AussieBookSeller, Truganina, VIC, Australien
Paperback. Zustand: new. Paperback. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis. The book is organized into chapters according to the most prominent presenting problem of patients with inherited metabolic diseases: neurologic, hepatic, cardiac, metabolic acidosis, dysmorphism, and acute catastrophic illness in the newborn. It also includes chapters on general principles, laboratory investigation, neonatal screening, and the principles of treatment. This new edition includes much greater depth on mitochondrial disease and congenital disorders of glycosylation. The chapters on neurological syndrome and newborn screening are greatly expanded, as are those on laboratory investigation and treatment, to take account of the very latest technological developments. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. To help make the correct diagnosis, the book is organized according to the clinical symptoms presenting in these patients. This new edition includes much new and up-dated material. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.
Verlag: Cambridge University Press, 2006
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - This user-friendly clinical handbook provides an overview of how to go about recognizing and diagnosing inherited metabolic diseases.
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In den WarenkorbPaperback. Zustand: Brand New. 3rd edition. 338 pages. 9.75x6.75x0.50 inches. In Stock. This item is printed on demand.
Verlag: Cambridge University Press, 2006
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
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In den WarenkorbPaperback / softback. Zustand: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days 745.
Verlag: Cambridge University Press, 2010
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
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In den WarenkorbKartoniert / Broschiert. Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. To help make the correct diagnosis, the book is organized according to the clinical symptoms presenting in.
Verlag: Cambridge University Press, 2010
ISBN 10: 0521614996 ISBN 13: 9780521614993
Sprache: Englisch
Anbieter: preigu, Osnabrück, Deutschland
Taschenbuch. Zustand: Neu. A Clinical Guide to Inherited Metabolic Diseases | Joe T. R. Clarke | Taschenbuch | Kartoniert / Broschiert | Englisch | 2010 | Cambridge University Press | EAN 9780521614993 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu Print on Demand.