123 results on '"Tada, K."'
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2. Solutions for problems caused by the distributed stray capacitance of oil-cooled and oil-immersed HVDC thyristor valves.
3. The minority carrier storage effect in the collector region and the storage time of transistors.
4. Thermal modulation spectroscopy of biological films
5. BUTADIENE-RUBBER MODIFIED WITH 1, 3-DIPOLAR CYCLOADDION REACTION
6. The Solution for the Problems Due to the Distributed Stray Capacitance on Oil-cooled and Oil-immersed HVDC Thyrister Valve
7. AUSTRALIA ANTIGEN IN AMNIOTIC FLUID
8. Reduction of the storage time of a transistor using a Schottky-barrier diode
9. Salmonella choleraesuisInfection of Pigs under Fattening
10. [Discussion: Nursing and the nurse].
11. A microangiographic and histologic study of the kidney in Kimmelstiel-Wilson disease.
12. Free amino acid levels in amniotic fluid of fetuses affected with Lowe's syndrome or Phenylketonuria.
13. Coexistence of defective activity in glycine-cleavage reaction and propionyl-CoA carboxylase in the liver of a hyperglycinemic child.
14. Maternal hyperphenylalaninemia induced experimentally: decreased incorporation of 14C-leucine into protein in the brain of the fetus.
15. [Treatment of urinary tract infections in children. Clinical experience with minocycline granules (author's transl)].
16. Ascending influenza spread in mice by intraperitoneal inoculation determined by immunofluorescence.
17. A block in glycine cleavage reaction as a common mechanism in ketotic and nonketotic hyperglycinemia.
18. [Pre- and post-operative nursing of patients with esophageal cancer].
19. [A case of testicular tumor in child].
20. [CLINICAL TRIAL OF OXYPHENBUTAZONE (TANDERIL) IN DERMATOLOGY].
21. A transport system common to imino acids and glycine.
22. ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY IN KLINEFELTER'S SYNDROME.
23. [Inborn error of amino acid metabolism with special reference to hyperglycinemia].
24. Nonaqueous polarography of quinones. IV. Polarography of p-benzoquinone and 1.4-naphthoquinone in glacial acetic acid and resonance effect upon half-wave potentials of p-quinones.
25. Enzymatic anomaly of erythrocytes in congenital nonspherocytic hemolytic anemia. 2.
26. Liver kynureninase activity of an infant with infantile spasm.
27. [B6-dependent xanthurenic aciduria].
28. [Hyperalaninemia-pyruvicemia: chronic lactic acidosis].
29. Cytological diagnosis of gastric cancer.
30. [BIBLIOGRAPHY OF DUTCH WRITINGS ON JAPAN. 70].
31. [Studies on the substances affecting the episomic infective transfer system. I. The relationship between the chemical structures of acridine derivatives and the inhibitory action on the multiple-drug-resistance transfer].
32. Activities of hypoxanthine-guanine phosphoribosyltransferase and adenine phosphoribosyltransferase in erythrocytes from patients with Down's syndrome.
33. Demonstration of metabolic anomaly of congenital nonspherocytic hemolytic anemia and beneficial effect of vitamin B12 upon it.
34. [Problems in reconstructive surgery of the hemiplegic upper extremity].
35. [Studies on the reticulocyte. II. The activities of enzymes and the contents of glutathione and of pyridine].
36. [Variations of the serum enzyme activity observed during hemolysis].
37. [On the influence of NaF on Ehrlich's ascitic cancer].
38. Formiminotransferase-deficiency syndrome: a new inborn error of folic acid metabolism.
39. Prolinuria: defect in intestinal absorption of imino acids and glycine.
40. 14CO2 in expired air after radioactive histidine injection in formiminotransferase deficiency syndrome.
41. THE RELATIONSHIP BETWEEN ELECTRON SPIN RESONANCE SIGNALS AND HAEMOPROTEIN OF LIVER MICROSOMES.
42. Vitamin B6 dependent xanthurenic aciduria (the second report).
43. Anemia of premature infant: the glucose-6-phosphate dehydrogenase activity in erythrocytes of cmrd blood from premature and full-term infants.
44. Prolinuria: transport of proline by leukocytes.
45. Tryptophan pyrrolase activity in rats subjected to electric convulsions.
46. [Inborn errors of amino acid metabolism--pathogenesis of mental retardation].
47. CONGENITAL TRYPTOPHANURIA WITH DWARFISM ("H" DISEASE-LIKE CLINICAL FEATURES WITHOUT INDICANURIA AND GENERALIZED AMINOACIDURIA):--A PROBABLY NEW INBORN ERROR OF TRYPTOPHAN METABOLISM.
48. [Studies on the reticulocyte. I. The MCV, MCH, MCHC and osmotic fragility of the reticulocyte].
49. A new entity of antibody deficiency syndrome, to which "congenital dysgammaglobulinemia" might be suggested.
50. Indicanuria in phenylketonuria.
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