Clinical studies in medical biochemistry /

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...

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Bibliographic Details
Call Number:Libro Electrónico
Other Authors: Glew, Robert H., Rosenthal, Miriam D.
Format: Electronic eBook
Language:Inglés
Published: New York : Oxford University Press, 2007.
Edition:3rd ed.
Subjects:
Clinical biochemistry > Case studies.
Biochemistry.
Metabolism > Disorders.
Biochemistry
Laboratory Techniques and Procedures
Metabolic Diseases
Biochimie clinique > Études de cas.
Biochimie.
Troubles du métabolisme.
biochemistry.
MEDICAL > Biochemistry.
Metabolism > Disorders
Clinical biochemistry
Electronic books.
Case Reports
Case studies
Case studies.
Études de cas.
Online Access:Texto completo
Table of Contents:
  • 10. Neonatal Hypoglycemia and the Importance of GluconeogenesisPart III: Intermediary Metabolism; 11. Glucose 6-Phosphate Dehydrogenase Deficiency and Oxidative Hemolysis; 12. Biotinidase Deficiency: A Biotin-Responsive Disorder; 13. Adrenoleukodystrophy; 14. Low-Density Lipoprotein Receptors and Familial Hypercholesterolemia; 15. Tangier Disease: A Disorder in the Reverse Cholesterol Transport Pathway; 16. Gaucher Disease: A Sphingolipidosis; 17. I-Cell Disease (Mucolipidosis II); 18. Inborn Errors of Urea Synthesis; 19. Phenylketonuria; 20. HMG-CoA Lyase Deficiency; 21. Hyperhomocysteinemia
  • 22. Neonatal HyperbilirubinemiaPart IV: Digestion, Absorption, and Nutritional Biochemistry; 23. Obesity: A Growing Problem; 24. Protein-Energy Malnutrition; 25. Lactose Intolerance; 26. Pancreatic Insufficiency Secondary to Chronic Pancreatitis; 27. Abetalipoproteinemia; 28. Vitamin B[sub(12)] Deficiency; 29. Vitamin A Deficiency in Children; 30. Calcium-Deficiency Rickets; 31. Hereditary Hemochromatosis; Part V: Endocrinology and Integration of Metabolism; 32. Type I Diabetes Mellitus; 33. Congenital Adrenal Hyperplasia: P450c21 Steroid Hydroxylase Deficiency; Index; A; B; C; D; E; F; G; H
  • IJ; K; L; M; N; O; P; R; S; T; U; V; X

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