148 results on '"Tazawa, Yusaku"'
Search Results
2. A novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: neonatal intrahepatic cholestasis caused by citrin deficiency
3. Cytoplasmic Inclusion Bodies and Minimal Hepatitis: Fibrinogen Storage without Hypofibrinogenemia
4. Neonatal presentation of adult-onset type II citrullinemia
5. Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC
6. Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency
7. Idiopathic Neonatal Hepatitis Presenting as Neonatal Hepatic Siderosis and Steatosis
8. Abstracts of selected papers presented at the 32nd Annual Meeting of the Japanese Society of Gastroenterology
9. Response of anti-oxidant enzymes mRNA in the neonatal rat liver exposed to 1,2,3,4-tetrachlorodibenzo-p-dioxin via lactation
10. Physical signs associated with excessive television-game playing and sleep deprivation
11. Effect of lactational exposure to 1,2,3,4- tetrachlorodibenzo-p-dioxin on cytochrome P-450 1A1 mRNA in the neonatal rat liver: Quantitative analysis by the competitive RT-PCR method
12. Infantile cholestatic jaundice associated with adult-onset type II citrullinemia
13. Excessive playing of home computer games by children presenting unexplained symptoms
14. Effect of weight reduction on serum transaminase activities in children with simple obesity
15. An undescribed subset of neonatal intrahepatic cholestasis associated with multiple hyperaminoacidemia
16. Urinary bile alcohol profiles in healthy and cholestatic children
17. Onset of Hemophagocytic Lymphohistiocytosis during Piperacillin-Tazobactam Therapy in Three Children with Acute Focal Bacterial Nephritis
18. Round-table discussion: “carry over” of liver disease in children to adulthood
19. Infantile liver disease: Carry-over to the adult. 2. Metabolic disease.
20. Eosinophilic Proctocolitis in 3-Months Japanese Infant; Report of a Case
21. Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients
22. Metabolic Liver Disease: Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition
23. Urinary organic acids in peroxisomal disorders: a simple screening method
24. Kanzo
25. A case of Reye's syndrome recieving aspirin.
26. Non-alcoholic steatohepatitis associated with hepatic fibrosis in two children.
27. Neonatal intrahepatic cholestasis with hepatic siderosis and steatosis
28. Effect of weight changes on serum transaminase activities in obese children
29. Heterogeneity of liver disorder in type B niemann-pick disease
30. Capillary Gas Chromatographic Determination of C27-Bile Acids in Biological Samples and Its Application to the Urine of a Patient with Zellweger Syndrome
31. Relationship of feeding modality to clinical features in Japanese infants with idiopathic neonatal hepatitis of the non-familial form
32. Relationships between clinical and histological profiles of non-familial idiopathic neonatal hepatitis
33. The relationship between serum transaminase activities and fatty liver in children with simple obesity
34. A Preterm Infant with Secondary Carnitine Deficiency due to MCT Formula. Effective Treatment of L-Carnitine.
35. A case of fatal infectious mononucleosis presenting with fulminant hepatic failure associated with an extensive CD8-positive lymphocyte infiltration in the liver
36. Hepatocellular Carcinoma in Children with Hepatitis B Surface Antigen.
37. An Acute Form of Tyrosinemia Type I With Multiple Intrahepatic Mass Lesions
38. A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency
39. Subclinical liver dysfunction in one-month-old infants with a low activity of vitamin K dependent coagulant factors assessed by normotest.
40. Studies on Steroids CCXXXXIV. Separation and Characterization of C-25 Epimers of Unconjugated and Conjugated Trihydroxycholestanoic Acids in Urine from a Patient with Zell Weger Syndrome by High-Performance Liquid Chromatography.
41. Occurrence of Both (25R)- and (25S)-3α,7α,12α-Trihydroxy-5β-Cholestanoic Acids in Urine from an Infant with Zellweger's Syndrome.
42. Application of the New Oral Pancreatic Exocrine Function Test 'PFD' Test in Children-Normal Values in Children-.
43. Alterations of serum bile acid profile in breast-fed infants with prolonged jaundice.
44. Bile acid profiles in siblings with progressive intrahepatic cholestasis: absence of biliary chenodeoxycholate.
45. Familial intrahepatic cholestasis associated with progressive neuromuscular disease and vitamin E deficiency.
46. Fecal and biliary bile acid patterns in children with bile acid malabsorption.
47. Serum bile acid patterns determined by an enzymatic method and high-performance liquid chromatography in young infants with cholestasis.
48. Serum Bile Acid Patterns Determined by an Enzymatic Method and HighPerformance Liquid Chromatography in Young Infants with Cholestasis
49. Alterations of Serum Bile Acid Profile in BreastFed Infants with Prolonged Jaundice
50. Syndrome of Inappropriate Secretion of Antidiuretic Hormone (SIADH) in a Case with Guillain‐Barre Syndrome
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