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J-GLOBAL ID:201402226335007972   Reference number:14A0414414

Cholelithiasis in a Patient with Type 2 Gaucher Disease

2型ゴーシェ病患者における胆石症
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Material:
Volume: 81  Issue:Page: 40-42 (J-STAGE)  Publication year: 2014 
JST Material Number: F0887A  ISSN: 1345-4676  CODEN: JNMSF5  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Congenital diseases,deformities in general.  ,  Pediatrics in general.  ,  Clinical medicine on digestive system in general 
Reference (10):
  • 1. Brady RO, Kanfer JN, Shapiro D: Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's disease. Biochem Biophys Res Commun 1965; 18: 221-225.
  • 2. Brady RO, Barton NW, Grabowski GA: The role of neurogenetics in Gaucher disease. Arch Neurol 1993; 5011: 1212-1224.
  • 3. Barton NW, Brady RO, Dambrosia JM, et al.: Replacement therapy for inherited enzyme deficiency-macrophage-targeted glucocerebrosidase for Gaucher's disease. N Engl J Med 1991; 324: 1464-1470.
  • 4. Erikson A, Johansson K, Månsson JE, Svennerholm L: Enzyme replacement therapy of infantile Gaucher disease. Neuropediatrics 1993; 24: 237-238.
  • 5. Rosenbaum H, Sidransky E: Cholelithiasis in patients with Gaucher Disease. Blood Cells Mol Dis 2002; 28: 21-27.
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