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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...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
New York :
Oxford University Press,
2007.
|
| Edición: | 3rd ed. |
| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- 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