Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases

Häftad, Engelska, 2016

2 180 kr

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Beskrivning

This book, combining and updating two previous editions, is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for both clinicians and laboratory personnel.

Produktinformation

Utgivningsdatum:2016-08-23
Mått:210 x 279 x 48 mm
Vikt:2 340 g
Format:Häftad
Språk:Engelska
Antal sidor:867
Förlag:Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
ISBN:9783662506882

Utforska kategorier

Sjukdomar och rubbningar inom Medicin
Kemi inom Naturvetenskap och teknik
Medicinsk utrustning och medicinska tekniker inom Medicin

Recensioner i media

From the book reviews: "It is a unique source of information on the diagnosis, treatment, and follow-up of patients with inherited metabolic diseases. ... much of the information is presented in tables which gives a good overview and makes the information easily readable. ... the book supplies clinicians and clinical biochemists with data that should facilitate the diagnosis and treatment of patients with inherited metabolic diseases." (Christian Staufner and Verena Peters, Journal of Inherited Metabolic Disease, Vol. 37, 2014)

Innehållsförteckning

Introductory Chapters.- Amino acids.- Organic acids.- Vitamins and neurotransmitter.- Energy metabolism.- Organelles.- Selected disorder.- Biochemical phenotypes of questionable clinical significance.- Profiles.