This edition uses actual clinical cases to illustrate important principles of biochemistry and molecular biology in the context of human disease. The format of each chapter remains the same - case presentation, diagnosis, therapy and references.
| 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 | |
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