Clinical Studies in Medical Biochemistry

Name: Clinical Studies in Medical Biochemistry
Price: 5.7 USD
Availability: InStock
ISBN: 9780195176889

ISBN-10: 019517688X

ISBN-13: 9780195176889

Edition: 3rd 2006

Authors: Robert H. Glew, Miriam D. Rosenthal

List price: $58.00

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This text uses a case-study approach to present the core principles of biochemistry and molecular biology in the context of human disease to students who will be involved in patient care. The 33 cases are carefully selected to cover key concepts and common diseases. Each chapter provides a specific patient report that includes the relevant history, pertinent clinical laboratory data, physical findings, and subsequent diagnosis. This is followed by a comprehensive discussion of thenormal biochemical processes and reactions pertaining to the case, along with the pathophysiological mechanisms of the disease.In this third edition of the book, a new co-editor has aided in the substantially…

Book details

List price: $58.00
Edition: 3rd
Copyright year: 2006
Publisher: Oxford University Press, Incorporated
Publication date: 8/24/2006
Binding: Paperback
Pages: 392
Size: 9.80" wide x 6.81" long x 0.91" tall
Weight: 1.694
Language: English




Protein Structure And Function



Creatine Kinase Isoenzymes and the Diagnosis of Myocardial Infarction




Hyaline Membrane Disease of the Newoborn




The Role of Biochemical Markers in the Management of Cancer




Congenital Dysfibrinogenemia




Sickle Cell Anemia




Bacterial Toxins: Diphtheria and Cholera




Metabolism And Energetics



Neonatal Hypoglycemia and the Importance of Gluconeogenesis




Pyruvate Dehydrogenase Complex Definciency and Congenital Lactic Acidosis




Glucose-6-Phosphate Dehydrogenase Deficiency




Biotin and Multiple Carboxylase Deficiency




Systemic Carnitine Deficiency--A Treatable Disorder




Diabetes Mellitus




Synthesis And Catabolism Of Complex Molecules



Alpha l-Antitrypsin Deficiency




Mannose-6-Phosphate Receptors and I-Cell Disease




Gaucher's Disease--A Sphingolipidosis




Atypical Phenylketonuria: A Dihydropteridine Reductase Deficiency




Marfan Syndrome and Homocystinuria: Pleiotropy, Variability and Genetic Heterogeneity




Treatment of Inborn Errors of Urea Synthesis




Steroids



Low Density Lipoprotein Receptors and Familial Hypercholesterolemia




Rickets Caused by a Deficiency of Vitamin D




Cushing's Syndrome




Aspects Of Inflammation And Pharmacology



Human Essential Fatty Acid Deficiencies of Dietary and Metabolic Origin




Anaphylaxis




Chronic Granulomatous Disease and Cytochrome b-245




Inhibitors of Angiotensin Converting Enzyme in the Management of Hypertension