400 results on '"Naito E"'
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2. Proton penetration efficiency over a high altitude observatory in Mexico
3. In-Process Monitoring of a Tissue-Engineered Oral Mucosa Fabricated on a Micropatterned Collagen Scaffold: Use of Optical Coherence Tomography for Quality Control
4. Type II Citrullinaemia (Citrin Deficiency) in a Neonate with Hypergalactosaemia Detected by Mass Screening
5. A novel dimorphism in the human SRY gene: usefulness in human migration studies
6. Beneficial effect of oral administration of Lactobacillus casei strain Shirota on insulin resistance in diet-induced obesity mice
7. Thiamine-responsive lactic acidaemia: role of pyruvate dehydrogenase complex
8. Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency
9. DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia
10. Molecular genetic analysis of a female patient with pyruvate dehydrogenase deficiency: detection of a new mutation and differential expression of mutant gene product in cultured cells
11. Mutation of E1α gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein
12. Multiple enzyme defects in mitochondria of a case with congenital lactic acidosis and hyperammonaemia
13. Effects of deoxyadenosine on ribonucleotide reductase in adenosine deaminase-deficient lymphocytes
14. Elevated cerebrospinal fluid lactate/pyruvate ratio in Machado-Joseph disease
15. Feeling the waist shrinking: The construction of the body image in the parietal cortex
16. Biochemical and molecular analysis of 12 patients with thiamine-responsive pyruvate dehydrogenase complex deficiency
17. CLONING OF A cDNA FOR HUMAN PYRUVATE DEHYDROGENASE PHOSPHATASE AND DETECTION OF A MUTATION IN A PATIENT WITH CONGENITAL LACTIC ACIDEMIA
18. Treatment of chronic congenital lactic acidosis by oral administration of dichloroacetate
19. Effects of lactic acid bacteria on low-density lipoprotein susceptibility to oxidation and aortic fatty lesion formation in hyperlipidemic hamsters
20. Urinary homocystine levels in a newborn infant with cystathionine synthase deficiency
21. PO175 SITAGLIPTIN IMPROVES DAILY GLUCOSE FLUCTUATION IN JAPANESE TYPE 2 DIABETIC OUTPATIENTS INADEQUATELY CONTROLLED WITH INSULIN THERAPY
22. De novo mtDNA nt 8993 (T-->G) mutation resulting in Leigh syndrome
23. Feeling the force: Returning haptic signals influence effort inference during motor coordination
24. Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency
25. Production of cyclic nucleotides from normal human brain.
26. Elevated cerebrospinal fluid lactate/pyruvate ratio in Machado-Joseph disease
27. Activity in the Posterior Parietal Cortex Mediates Visual Dominance over Kinesthesia
28. Somatic Sensation of Hand-Object Interactive Movement Is Associated with Activity in the Left Inferior Parietal Cortex
29. In vitro activation of the pyruvate dehydrogenase complex in human muscle by a broad specificity protein phosphatase
30. Association Between Vitamin D Receptor Genotype and Age of Onset in Juvenile Japanese Patients With Type 1 Diabetes
31. Platform for timely portable-push information delivery.
32. Gender-Specific Occurrence of West Syndrome in Patients with Pyruvate Dehydrogenase Complex Deficiency
33. Perceptual changes in illusory wrist flexion angles resulting from motor imagery of the same wrist movements
34. Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiency
35. Functional representations involved in the perception of vibration-induced illusory arm movements
36. Differential activation of somatosensory areas depending on object shape: Cytoarchitectonic mapping and PET
37. Somatosensory areas activated due to moving stimuli on the skin A study using cytoarchitectonic mapping and PET
38. Correlation of the rCBF in anterior cingulate cortex with reaction time
39. Decreases of regional blood flow of the lateral cerebellum associated with pure motor learning using the Chian-Xin-Qiu
40. Response to Kordonouri et al.
41. Relationship Between GAD Antibody and Residual -CellFunction in Children After Overt Onset of IDDM
42. Molecular genetic analysis of a female patient with pyruvate dehydrogenase deficiency: detection of a new mutation and differential expression of mutant gene product in cultured cells
43. Choroidal and optic disc metastases from breast cancer and their response to combination pharmacotherapy with tamoxifen, cyclophosphamide hydrate, letrozole, and bevacizumab.
44. Therapeutic Effect of Sodium Dichloroacetate on Visual and Auditory Hallucinations in a Patient with MELAS
45. Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency.
46. Effects of deoxyadenosine on ribonucleotide reductase in adenosine deaminase‐deficient lymphocytes
47. Gender-Specific Occurrence of West Syndrome in Patients with Pyruvate Dehydrogenase Complex Deficiency.
48. Mitochondrial myopathy and familial thiamine deficiency.
49. Comparison of GAD and ICA512/IA-2 antibodies at and after the onset of IDDM.
50. 1a-Hydroxyvitamin D (sub 3) Treatment of Three Patients With 1,25-Dihydroxyvitamin D-Receptor-Defect Rickets and Alopecia.
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