A Clinical Guide to Inherited Metabolic Diseases

Clarke, Joe T. R.

ISBN 10: 0521614996 ISBN 13: 9780521614993
Editore: Cambridge University Press, 2005
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Former library book; may include library markings. Used book that is in clean, average condition without any missing pages. Codice articolo GRP82747924

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This user-friendly clinical handbook provides an overview of how to go about recognizing and diagnosing inherited metabolic diseases.

Recensione: '... should be read thoroughly by any pediatric resident, genetic resident, or clinical fellow caring for patients with metabolic disorders.' American Journal of Medical Genetics

'In short, this is an excellent guide to metabolic disease; it represents good value for money and, I suspect, will be more likely found in the owner's pocket rather than on the shelf. It is recommended not only to the 'busy physician' and trainee, but to all those with an interest in metabolic disease.' Journal of Inherited Metabolic Disease

'The writing is lucid, direct and salted with personal observations. Clarke's teaching skills shine forth from each page ... It succeeds admirably, effectively demystifying the anxiety-provoking world of inherited biochemical illness.' Canadian Medical Association Journal

'... 280-page clinical guide ... On the whole, I found this to be an amazing book which contains a vast amount of information presented in a concise, logical and well-organized fashion ... I would recommend this book wholeheartedly to anyone involved in the diagnosis of inherited metabolic diseases.' Journal of Genetic Counseling

'Dr Clarke's enthusiasm and erudition are evident on every page of this book.' Archives of Diseases of Childhood

'An excellent book for physicians who find inherited metabolic diseases intimidating ...The information is presented in such a clear and simple fashion that few people would find this book difficult to read ...Clarke teaches a complex subject in a simple but complete manner.' Canadian Medical Association Journal

'If your clinical work brings you into contact with patients who may be hiding an inherited metabolic disease, Clarke's Guide is clearly for you.' Journal of the Royal Society of Medicine

'This books strength lies in its simple straightforward clinical approach to this difficult area of medicine.' Doctors.net.uk

To guide the reader in this assessment, a compact volume such as has been written by Dr Clarke is invaluable. Dr Clarke has succeeded in providing the reader with a user-friendly, inexpensive book that is up to date, and provides directions for further reading.' European Journal of Paediatric Neurology

'Joe T. R. Clarke, is an experienced clinician and educator, and this is evident in the amount of detail and clear explanation provided throughout the work. ... it is very readable and would be a valuable addition to the library of anyone involved in genetic counselling, nurses who care for patients with inherited metabolic disease and those involved in newborn screening.' Nursing Standard

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Dati bibliografici

Titolo: A Clinical Guide to Inherited Metabolic ...
Casa editrice: Cambridge University Press
Data di pubblicazione: 2005
Legatura: Brossura
Condizione: Good
Edizione: terza edizione

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Clarke, J. T. R.
ISBN 10: 0521614996 ISBN 13: 9780521614993
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Condizione: Poor. This is an ex-library book and may have the usual library/used-book markings inside.This book has soft covers. In poor condition, suitable as a reading copy. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,850grams, ISBN:9780521614993. Codice articolo 8724164

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Paperback. Condizione: Brand New. 3rd edition. 338 pages. 9.75x6.75x0.50 inches. In Stock. This item is printed on demand. Codice articolo __0521614996

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Clarke, Joe T. R.
ISBN 10: 0521614996 ISBN 13: 9780521614993
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Kartoniert / Broschiert. Condizione: 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. Codice articolo 446942296

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Paperback. Condizione: 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. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Codice articolo 9780521614993

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Joe T. R. Clarke
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Taschenbuch. Condizione: 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. Codice articolo 102294140

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Paperback. Condizione: 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. Codice articolo 9780521614993

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Paperback. Condizione: 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. This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability. Codice articolo 9780521614993

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Taschenbuch. Condizione: 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. Codice articolo 9780521614993

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