NNIW50 - Metabolic Disorders Diseases in Infant and Child Nutrition

Subject Index

Concluding Discussion

Gene Therapy: A Potential Solution for Nutrition-Dependent Disorders?

Diet, Gene Expression, and Apoptosis: Clues to Cancer Prevention?

Diet as a Determinant of Drug Response

Current Uses and Future Perspectives of Recombinant Modifications in Food Production

Genetic Variations of Gliadins: New Approaches for the Treatment of Celiac Disease

Current Understanding of the Molecular and Cellular Basis of Celiac Disease

From Arginine to Creatine: Regional and Cellular Gene Expression of Enzymes and Transporters Linking Nitrogen and Energy Metabolism in Brain

Carbohydrate Therapy of Congenital Disorders of Glycosylation

Genetic Variability of Human Milk Oligosaccharides: Are There Biologic Consequences?

Oxidative Stress: Antioxidants In Degenerative Neurologic And Ophthalmologic Diseases

Long-Chain Omega-3 Fatty Acids Are Conditionally Essential Substrates in Children: Effects on Visual Function in Children with Phenylketonuria

Genetic Disorders of Mitochondrial and Peroxisomal Fatty Acid Oxidation and Peroxisome Proliferator-Activated Receptors

Fatty Acid Regulation of Gene Expression: A Genomic Mechanism to Improve the Metabolic Syndrome

How to Assess Amino Acid Requirements (With Particular Reference to Inborn Errors of Amino Acid Metabolism)

Minimum Protein Requirements in Infancy and Childhood: Insights from Patients with Protein-Restricted Diets

Genetic Variation of Homocysteine Metabolism and Atherosclerosis

Metabolic Disorders Diseases in Infant and Child Nutrition