Clinical Studies in Medical Biochemistry
Oxford University Press Inc (Verlag)
978-0-19-509929-4 (ISBN)
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This text uses a case-study format to relate the fundamentals of biochemistry to the practice of medicine. cases, carefully selected to cover common diseases and important principles, follow a consistent format. Each chapter begins with a detailed case Report which describes the relevant history, physical findings, and laboratory findings. This is followed by a section on Diagnosis, which includes a brief discussion of differential diagnosis and criteria needed for establishing the diagnosis. The next section, Biochemical Perspectives, forms the heart of each chapter. A discussion of normal metabolic reactions, pathways, and the consequences of the defect is followed by a brief discussion of therapeutic options (Therapy). Each chapter ends with several discussion questions and a brief bibliography.
Robert H. Glew, Ph.D., is Professor and Chairman of the Department of Biochemistry at the University of New Mexico School of Medicine. Yoshifumi Ninomiya, Ph.D., M.D., is Professor and Chairman of the Department of Molecular Biology and Biochemistry at Okayama University Medical School, Japan.
PART I. NUCLEIC ACIDS, VIRUSES AND PROTEIN STRUCTURE AND FUNCTION; 1. Creatine Kinase Isoenzymes and the Diagnosis of Myocardial Infarction (Mercer/Varat/Amory); 2. Hereditary Spherocytosis (Ideguchi); 3. Fragile X Syndrome (Narahara/Yokoyama); 4. Human Immunodeficiency Viruses and the Acquired Immunodeficiency Syndrome (Jenison/Hjelle); 5. Pertussis (Kaslow/Pichichero); 6. Fulminant Hepatitis B (Mishiro/Kanai/Kojima); 7. Sickle Cell Anemia (Charache/Scott-Emuakpor); PART II. METABOLISM AND ENERGETICS; 8. Glucose 6-phosphate Dehydrogenase Deficiency (Beutler/Laubscer); 9. Neonatal Hypoglycemia (Holzman/Milley); 10. Jaundice and Gallstone Disease (Tazuma/Kajiyama); 11. Pernicious Anemia (VanderJagt/McCarthy); 12. Pyruvate Dehydrogenase Complex Deficiency; 13. Biotin and Multiple Carboxylase Deficiency (Dakshinamurti); 14. Lactose Intolerance (Woodfin/Arora); 15. Systemic Carnitine Deficiency (Paul/Sekas); 16. Diabetes Mellitus (Kitabchi/Fisher); PART III. METABOLISM OF COMPLEX MOLECULES; 17. Rhabdomyolysis (Murakami); 18. Abetalipoproteinemia: A Disorder of Lipoprotein Assembly (Remaley/Buley); 19. Low-density Lipoprotein Receptors and Familial Hypercholesterolemia (Margolis); 20. Alport Syndrome (Hereditary Nephritis) (Tryggvason/Ninomiya); 21. Pancreatic Exocrine Insufficiency (Reyes/Galey); 22. Lead Poisoning (Endo/Taketani); 23. Peroxisomal Disorders: Zellwger Syndrome and Adrenoleukodystropht (Suzuki/Orii); 24. Inborn Errors of Urea Synthesis (Brusilow); 25. Alpha 1-Antitrypsin Deficiency (Sharp/Schwarzenberg); 26. Gaucher Disease: A Sphingolipidosis (Scariano/Glew); 27. I-Cell Disease (Chambers/Williams); 28. Atypical Phenylketonuria (Remaley); PART IV. STEROIDS; 29. Cushing's Syndrome (Vela); 30. Rickets and Vitamin D (Chesney); PART V. ASPECTS OF INFECTION AND PHARMACOLOGY; 31. Angiotensin Converting Enzyme and Hypertension (Traub/Shapiro); 32. Chronic Granulomatous Disease (Thrasher/Segal)
| Erscheint lt. Verlag | 24.7.1997 |
|---|---|
| Co-Autor | Yoshifumi Ninoyama, Stephen P. Peters |
| Zusatzinfo | numerous black and white photographs, line figures and tables |
| Verlagsort | New York |
| Sprache | englisch |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete |
| Studium ► 1. Studienabschnitt (Vorklinik) ► Physiologie | |
| Naturwissenschaften ► Biologie ► Biochemie | |
| ISBN-10 | 0-19-509929-X / 019509929X |
| ISBN-13 | 978-0-19-509929-4 / 9780195099294 |
| Zustand | Neuware |
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