Clinical studies in medical biochemistry / edited by Robert H. Glew and Miriam D. Rosenthal.
Material type: TextPublication details: New York : Oxford University Press, 2007.Edition: 3rd edDescription: 1 online resource (1 volume)Content type:- text
- computer
- online resource
- 9780199749096
- 0199749094
- 612/.015 22
- RB112.5 .C57 2007eb
- QU 4
Item type | Home library | Collection | Call number | Materials specified | Status | Date due | Barcode | |
---|---|---|---|---|---|---|---|---|
Electronic-Books | OPJGU Sonepat- Campus | E-Books EBSCO | Available |
Includes bibliographical references and index.
Print version record.
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
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 patient report that includes the relevant history, pertinent clinical laboratory data, physical findings, and subsequent diagnosis. This is followed by a comprehensive discussion of the normal biochemical processes and reactions pertaining to the case, along with the pathophysiological mechanisms of.
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