472 results on '"Takada, G."'
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2. Posterior Descending Coronary Artery Flow Reserve Assessment by Doppler Echocardiography in Children with and without Congenital Heart Defect Comparison with Invasive Technique
3. Changes in Pulmonary Venous Flow Patterns in Patients with Ventricular Septal Defect
4. Body Mass Index Can Predict Left Ventricular Diastolic Filling in Asymptomatic Obese Children
5. 3-Methylglutaconic aciduria type I: Clinical heterogeneity as a neurometabolic disease
6. Practice of Free Jejunal Transfer for Esophageal Reconstruction
7. Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1
8. Increase in Pulmonary Arterial Diameter Under Prostaglandin E1 Therapy in Infants with Cyanotic Congenital Heart Disease
9. Postnatal Left Ventricular Contractility in Very Low Birth Weight Infants
10. Postnatal Changes in Left Ventricular Volume and Contractility in Healthy Term Infants
11. Acid sphingomyelinase deficiency: Cardiac dysfunction and characteristic findings of the coronary arteries
12. Effects of low-dose dobutamine on left ventricular diastolic filling in children
13. Role of gestational age and body weight on Doppler transmitral flow velocity pattern in very low birth weight infants
14. Development of an efficient production method for β-mannosidase by the creation of an overexpression system in Aspergillus aculeatus
15. Evaluation of alternative substrates for determining methane-oxidizing activities and methanotrophic populations in soils
16. Molecular and population genetics of phenylketonuria in Orientals: Correlation between phenotype and genotype
17. Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
18. A case of tubulo-interstitial nephritis with exfoliative dermatitis and hepatitis due to phenobarbital hypersensitivity
19. An SEDL gene mutation in a Japanese kindred of X-linked spondyloepiphyseal dysplasia tarda
20. An exonic mutation of the GH-1 gene causing familial isolated growth hormone deficiency type II
21. Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome
22. Cytotoxic activity against tumour cells mediated by intermediate TCR cells in the liver and spleen
23. Acute life-threatening event with rhabdomyolysis after starting on high-dose pyridoxine therapy in an infant with homocystinuria
24. Congenital atresia of left coronary ostium
25. Transient 5-oxoprolinuria in a very low-birthweight infant
26. Serum Zn2+-stimulated sphingomyelinase deficiency in type B Niemann-Pick disease
27. Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis
28. Role of local renin-angiotensin system in warm ischemia and reperfusion injury of the liver
29. Crystal Structure of D-tagatose 3-epimerase from Pseudomonas cichorii in Complex with D-fructose
30. Crystal structure of D-tagatose 3-epimerase from Pseudomonas cichorii at 1.79 A resolution
31. Crystal structure of D-tagatose 3-epimerase from Pseudomonas cichorii
32. Crystal structure of D-tagatose 3-epimerase from Pseudomonas cichorii with D-tagatose
33. Development of an efficient production method for ?-mannosidase by the creation of an overexpression system in Aspergillus aculeatus
34. Crystal structure of L-Rhamnose Isomerase from Pseudomonas stutzeri with L-Rhamnose
35. Crystal Structure of L-Rhamnose Isomerase from Pseudomonas stutzeri in Complex with D-Allose
36. Crystal structure of L-rhamnose isomerase from Pseudomonas stutzeri with metal ion
37. Niemann–Pick type C disease: Novel NPC1 mutations and characterization of the concomitant acid sphingomyelinase deficiency
38. P-89 An infant with radio-ulnarsynostosis and myelodysplastic syndrome (RCMD) had trisomy 8 and responded to immunosuppressive therapy
39. Johanson-Blizzard Syndrome: Loss of Glucagon Secretion Response to Insulin-induced Hypoglycemia
40. Pyruvate carboxylase activity in lymphoblasts
41. Juvenile Alexander disease with a novel mutation in glial fibrillary acidic protein gene
42. Assessment of global left ventricular function by tissue Doppler imaging
43. Variability of the Light Curves of the Close Binary GR Tauri
44. Serum Zn 2+ -stimulated sphingomyelinase deficiency in type B Niemann-Pick disease
45. Serum alanine aminotransferase activity in obese children
46. Prediction of adult height in healthy Japanese children
47. Morphological change of the 5th aortic arch with tetralogy of Fallot and pulmonary atresia: echocardiographic and angiographic findings
48. Abrupt aggravation of atrioventricular block and syncope in hypertrophic cardiomyopathy.
49. Left ventricular preload reserve in preterm infants with patent ductus arteriosus
50. Mutation of the Myelin Po Gene in Charcot-Marie-Tooth Neuropathy Type 1
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