The inherited metabolic diseases
Author(s)
Bibliographic Information
The inherited metabolic diseases
Churchill Livingstone, 1994
2nd ed
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Note
Includes bibliographical references and index
Description and Table of Contents
Description
This aims to provide a comprehensive account of the inherited metabolic diseases, fully revised for this second edition. 18 contributors from the UK and Europe have covered major developments including peroxisomal and respiratory chain disorders. The text is concise and, with the use of the bibliography to such important practical aspects as diagnosis and treatment, it should be a useful alternative source of reference.
Table of Contents
- Disorders of carbohydrate metabolism, D.B. Dunger and J.B. Holton
- amino acid disorders, R.J. Pollitt
- disorders of organic acid metabolism, R.A. Chalmers
- lysosomal storage disorders, C.A. Pennock
- peroxisomal disorders, R.B.H. Schutgens and R.J.A. Wanders
- defects of the mitochondrial respiratory chain, L.A. Bindoff and D.M. Turnbull
- purine and pyrimidine disorders, H.A. Simmonds
- the prophyrias, G.H. Elder
- collagen disorders, A.C. Nicholls
- inherited disorders of steroid biosynthesis, G.M. Addison
- lipid disorders, C.H. Bolton
- metal disorders, P.J. Aggett
- red cell disorders, A.J. Grimes and N.G.P. Slater.
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