141 results on '"Tada, K."'
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2. VP13.10: Prenatal ultrasound findings in a survived case of perinatal lethal hypophosphatasia with enzyme replacement therapy started early in life
3. VP15.21: Feasibility and efficacy of longitudinal strain measurement in fetal heart using two‐dimensional tissue tracking
4. OP16.09: Cardiac output and placental perfusion in growth‐restricted fetuses with cerebral blood flow redistribution
5. OC25.02: Estimated pulse wave velocity in growth‐restricted fetuses: a novel perspective for fetal hemodynamic changes using phased tracking method
6. P04.11: Increased fetal pulse wave velocity and pulse pressure in growth-restricted fetuses with heart-sparing effect
7. OC02.03: Distal right coronary arterial flow in growth-restricted fetuses: a feasible sign of heart-sparing effect with reserved heart function?
8. OP29.04: Prenatal demonstration of distal right coronary artery in growth‐restricted fetuses: a sign of protective response?
9. OP20.05: Prenatal demonstration of distal right coronary artery in normal and growth-restricted fetuses: a plausible sign of heart-sparing effect?
10. Spontaneous spin polarization and spin pumping effect on edges of graphene antidot lattices
11. ChemInform Abstract: A Facile Preparation of (E)-α-(1H-1,2,4-Triazol-1-yl)styryl Ketones Using Isomerization-Crystallization Method.
12. ChemInform Abstract: Nicotinamide Derivatives as a New Class of Gastric H+/K+-ATPase Inhibitors. Part 1. Synthesis and Structure-Activity Relationships of N-Substituted 2-(Benzhydryl- and benzylsulfinyl)nicotinamides.
13. CIH-Tokyo Experience with Breast-Conserving Surgery without Radiotherapy: 6.5 Year Follow-Up Results of 1462 Patients
14. Loading Fullerene into a Conjugated Polymer Without Chemical Modification
15. The effect of swirl flow in an immersion nozzle on the heat and fluid flow in a billet continuous casting mold
16. Nanostructured Conjugated Polymer Films by Electrophoretic Deposition
17. Biodegradability of scott-gelead photodegradable polyethylene and polyethylene wax by microorganisms
18. Association Between Drinking-Related Antisocial Behavior and a Polymorphism in the Serotonin Transporter Gene in a Japanese Population
19. An 84bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNA
20. Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics
21. ChemInform Abstract: Nicotinamide Derivatives as a New Class of Gastric (H+/K+)‐ATPase Inhibitors. Part 3. Synthesis and Gastric Antisecretory Activity of 2‐( (2‐ and 4‐Aminobenzyl, and α‐Methylbenzyl)sulfinyl)‐N‐(4‐ pyridinyl)‐3‐pyridinecarboxamides (I).
22. ChemInform Abstract: Nicotinamide Derivatives as a New Class of Gastric (H+/K+)‐ATPase Inhibitors. Part 2. Synthesis and Structure‐Activity Relationships of 2‐((2,4‐Dimethoxybenzyl)sulfinyl)‐N‐(4‐pyridinyl)pyridine‐3‐ carboxamides.
23. Role of screening for hepatitis C virus in children with malignant disease and who undergo bone marrow transplantation
24. Diabetes mellitus associated with mitochondrial myopathy and schizophrenia: a possible link between diabetes mellitus and schizophrenia
25. ChemInform Abstract: A Convenient Synthesis of N‐Substituted 2,3‐Dihydro‐3‐oxoisothiazolo(5, 4‐b)pyridines in Acidic Conditions.
26. Delayed Diagnosis of Isolated ACTH Deficiency in a Patient with Diabetes Mellitus
27. Prenatal diagnosis in a new peroxisomal disease by the W‐particle separation method
28. Influence of ageing on onset of mitochondrial disease
29. Enrichment of helium by asymmetric hollow-fiber membrane of cellulose triacetate
30. Clinical and biochemical phenotype of the MELAS mutation
31. Propionic acidaemia: Sequence analysis of mutant mRNAs from Japanese β subunit‐deficient patients
32. Non‐ketotic hyperglycinaemia: Molecular lesion, diagnosis and pathophysiology
33. Defects of mitochondrial respiratory enzymes in cloned cells from MELAS fibroblasts
34. Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty‐nine Japanese patients with urea cycle enzymopathies
35. A new type of mitochondrial DNA deletion in patients with encephalomyopathy
36. First-trimester prenatal diagnosis in quintuplets: A practical approach using step-by-step embryo reduction
37. A four‐nucleotide insertion at the E 1 α gene in a patient with pyruvate dehydrogenase deficiency
38. Retrospective survey of urea cycle disorders: Part 1. Clinical and laboratory observations of thirty-two Japanese male patients with ornithine transcarbamylase deficiency
39. Genomic analysis of non‐ketotic hyperglycinaemia: A partial deletion of P‐protein gene
40. Molecular analysis of dihydropteridine reductase deficiency and restoration of the enzyme activity by gene transfer
41. Simple and rapid detection of phenylketonuria mutation tightly linked to haplotype 2 by modified polymerase chain reaction
42. Fall and Rise Variations of Serum GGTP in Preoperative Infants with Biliary Atresia
43. The abnormality of peroxisomal membrane proteins in Zellweger syndrome
44. A new variant of glycogen storage disease type 1: Probably due to a defect in the glucose‐6‐phosphate transport system
45. Unconjugated, Glycine-conjugated, Taurine-conjugated Bile Acid Nonsulfates and Sulfates in Urine of Young Infants with Cholestasis
46. Hyperornithinaemia with gyrate atrophy: Pathophysiology and treatment
47. Epstein‐Barr Virus‐induced Lymphoblastoid Cell Lines from Patients with Primary Immunodeficiency Diseases
48. Immunochemical study in three patients with cytochrome c oxidase deficiency presenting leigh's encephalomyelopathy
49. A Survey on Prenatal Diagnosis of Inherited Metabolic Diseases in Japan
50. S‐Adenosylhomocysteine hydrolase activity in a lymphoblastoid cell line from a patient with adenosine deaminase deficiency disease
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