46 results on '"Tada, K."'
Search Results
2. Nonketotic Hyperglycinemia
3. Nonketotic Hyperglycinemia
4. Hartnup Disease
5. Disorders of Purine and Pyrimidine Metabolism
6. Branched-Chain Organic Acidurias
7. The Respiratory Chain
8. Ketolysis Defects
9. Disorders of Galactose Metabolism
10. Inherited Disorders of Cobalamin and Folate Absorption and Metabolism
11. Disorders of the Gamma Glutamyl Cycle
12. Biotin-Responsive Multiple Carboxylase Deficiency
13. Dyslipidemias
14. Glutaric Aciduria Type I and Related Cerebral Organic Acid Disorders
15. Glycogen Storage Diseases
16. Hyperphenylalaninaemias
17. Urea Cycle Disorders
18. Homocystinuria Due to Cystathionine β-Synthase Deficiency and Related Disorders
19. Somatic Gene Therapy
20. Ornithine
21. Tyrosine
22. Disorders of Fatty Acid Oxidation
23. The Pyruvate Dehydrogenase Complex and Tricarboxylic Acid Cycle
24. Disorders of Gluconeogenesis
25. Disorders of Fructose Metabolism
26. Liver Transplantation
27. Emergency Treatments
28. Oxalosis (Primary Hyperoxaluria)
29. Inborn Errors of Bile Acid Synthesis
30. Bone Marrow Transplantation
31. Porphyrias
32. Peroxisomal Disorders
33. Cystinosis
34. Sphingolipids
35. Bilirubin
36. Mucopolysaccharides and Oligosaccharides
37. Transport Defects of Amino Acids at the Cell Membrane: Cystinuria, Hartnup Disease, and Lysinuric Protein Intolerance
38. Copper: Wilson and Menkes Diseases
39. Disorders of Neurotransmitters
40. Genetic Defects Related to Metals Other Than Copper
41. Diagnostic Procedures: Function Tests and Postmortem Protocol
42. Clinical Approach to Inherited Metabolic Diseases
43. Psychosocial Care of the Child and Family
44. Disorders of Small Peptides
45. Carbohydrate-Deficient Glycoprotein Syndromes
46. Alpha-1-Antitrypsin Deficiency
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