Clinical Studies in Medical Biochemistry
Robert H. Glew(Autor*in)
Oxford University Press Inc
Erschienen am 10. Dezember 1987
Buch
Softcover
352 Seiten
978-0-19-503922-1 (ISBN)
Artikel ist vergriffen; siehe Neuauflage
Beschreibung
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.
Weitere Details
Sprache
Englisch
Verlagsort
New York
USA
Zielgruppe
Für höhere Schule und Studium
Für Beruf und Forschung
Illustrationen
18 halftones, 77 line illustrations
ISBN-13
978-0-19-503922-1 (9780195039221)
Copyright in bibliographic data is held by Nielsen Book Services Limited or its licensors: all rights reserved.
Schweitzer Klassifikation
Weitere Ausgaben
Nachauflagen
Robert H. Glew
Clinical Studies in Medical Biochemistry
Buch
03/1997
2. Auflage
Oxford University Press Inc
32,04 €
Artikel ist vergriffen; siehe Neuauflage
Personen
Inhalt
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.