Clinical studies in medical biochemistry

著者

書誌事項

Clinical studies in medical biochemistry

edited by Robert H. Glew, Yoshifumi Ninomiya

Oxford University Press, 1997

2nd ed

  • : pbk

大学図書館所蔵 件 / 全29件

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注記

Includes bibliographical references and index

内容説明・目次

内容説明

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.

目次

  • 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)

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