NNIW50 - Metabolic Disorders Diseases in Infant and Child Nutrition

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

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

Current Uses and Future Perspectives of Recombinant Modifications in Food Production

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

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

Carbohydrate Therapy of Congenital Disorders of Glycosylation

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)

Metabolic Disorders Diseases in Infant and Child Nutrition

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

Genetic Variation of Homocysteine Metabolism and Atherosclerosis

Subject Index

Concluding Discussion