Inborn Metabolic Diseases: Diagnosis and Treatment

Author:   Jean-Marie Saudubray ,  Georges Van Den Berghe ,  John H. Walter
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Edition:   5th ed. 2012
ISBN:  

9783642157196


Pages:   684
Publication Date:   23 November 2011
Format:   Hardback
Availability:   Awaiting stock   Availability explained
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Inborn Metabolic Diseases: Diagnosis and Treatment


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Author:   Jean-Marie Saudubray ,  Georges Van Den Berghe ,  John H. Walter
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Imprint:   Springer-Verlag Berlin and Heidelberg GmbH & Co. K
Edition:   5th ed. 2012
Dimensions:   Width: 19.30cm , Height: 3.80cm , Length: 26.00cm
Weight:   1.633kg
ISBN:  

9783642157196


ISBN 10:   364215719
Pages:   684
Publication Date:   23 November 2011
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Awaiting stock   Availability explained
The supplier is currently out of stock of this item. It will be ordered for you and placed on backorder. Once it does come back in stock, we will ship it out for you.

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Reviews

From the reviews of the fifth edition: This clearly written update on a highly complex group of inherited metabolic disorders describes childhood-onset and adult-onset inherited conditions. ... the book is most useful for pediatric subspecialists (e.g., clinical geneticists, neurologists), although it covers adult-onset metabolic diseases as well. ... This is an outstanding book about the complex and mostly newly described field of clinical biochemical genetics. This fifth edition offers the most current overview of a rapidly evolving specialty which has relevance to all areas of medical practice. (Hans Christoph Andersson, Doody's Review Service, October, 2012)


Author Information

Professor Jean-Marie Saudubray, M.D., Director of the Metabolic/Diabetes Unit, Dep. of Pediatrics, Hopital Necker Enfants Malades, Paris, France Professor Georges van den Berghe, Professor, Metabolic Research Group, University of Louvain Medical School, Brussels, Belgium Dr. John H. Walter, Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Manchester, Great Britain

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