Clinical studies in medical biochemistry
著者
書誌事項
Clinical studies in medical biochemistry
Oxford University Press, 1987
- pbk.
大学図書館所蔵 全9件
注記
Includes bibliographies and index
内容説明・目次
内容説明
Intended for use as a supplement in medical-school biochemistry courses, Clinical Studies in Medical Biochemistry uses a case-study format to relate the fundamentals of biochemistry to the practice of medicine. The thirty cases, carefully selected to cover common diseases and important principles, follow a consistent format: a case report, presenting the history, physical findings, and relevant laboratory data; diagnosis; a discussion of the biochemical perspectives; therapeutic options; questions and bibliography. The chapter authors have been selected for their significant contributions to the understanding of the diseases they write about.
目次
- PART I: PROTEIN STRUCTURE AND FUNCTION
- D.W. Mercer & M.A. Varat: creatine kinase isoenzymes and the diagnosis of myocardial infarction
- J.U. Balis, S.A. Shelley & K.S. Kanarek: hyaline membrane disease of the newborn
- D.W. Mercer & T.S. Talamo: the role of biochemical markers in the management of cancer
- R.F. Ebert & W.R. Bell: congenital dysfibrinogenemia
- S. Charache & S.L. Phillips: sickle cell anaemia
- R. Jagus, J.N. Dowling, J. Moss, & M. Vaughan: bacterial toxins: diphtheris and cholera
- PART II: METABOLISM AND ENERGETICS
- I.R. Holzman & J.R. Milley: neonatal hypoglycaemia and the importance of gluconeogenesis
- J.H. Collins: pyruvate dehydrogenase complex deficiency and congenital lactic acidosis
- E. Beutler: glucose-6-phosphate dehydrogenase deficiency
- J.G. Thoene & D.N. Buchanan: biotin and multiple carboxylase deficiency
- H.S. Paul: systemic carniture deficiency - a treatable disorder
- A.E. Kitabchi & J.N. Fisher: diabetes mellitus
- PART III: SYNTHESIS AND CATABOLISM OF COMPLEX MOLECULES
- S.J. Schwarzenberg & H.L. Sharp: alpha 1-antitrypsin deficiency
- B.F. Mandell: mannose-6-phosphate receptors and I-cell disease
- K.L. LaMarco & R.H. Glew: Gaucher's disease - a Sphingolipidosis
- A.T. Remaley & K.L. LaMarco: atypical phenylketonuria: a dihydropteridine reductase deficiency
- R. E. Pyeritz: Marfan syndrome and homocystinuria: pleiotropy, variability and genetic heterogeneity
- G.P. Beliveau & S.W. Brusilow: treatment of inborn errors of urea synthesis
- PART IV: STEROIDS
- J.J.S. Chen & S. Margolis: low density lipoprotein receptors and familial hypercholesterolaemia
- R. W. Chesney & S. Dabbagh: rickets caused by a deficiency of vitamin D
- F. Short & V.H.T. James: Cushing's syndrome
- PART V: ASPECTS OF INFLAMMATION AND PHARMACOLOGY
- R.T. Holman & A.B. Christophe: human essential fatty acid deficiencies of dietary and metabolic origin
- P.S. Creticos & S.P. Peters: Anaphylaxis
- A. Segal: chronic granulomatus disease and cytochrome 6-245
- A.P. Shapiro: inhibitors of angiotensin converting enzyme in the management of hypertension.
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