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J-GLOBAL ID:201202233567053590   Reference number:12A0238480

Diagnosis and Management of Type I and Type V Hyperlipoproteinemia

I型およびV型の高リポ蛋白血症の診断と管理
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Material:
Volume: 19  Issue:Page: 1-12 (J-STAGE)  Publication year: 2012 
JST Material Number: U0153A  ISSN: 1880-3873  Document type: Article
Article type: 解説  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Metabolic diseases,nutritional diseases in general. 
Reference (45):
  • 1) Fredrickson DS, Lees RS: Familial hyperlipoproteinemia. in The Metabolic Basis of Inherited Disease (ed. by Stanbury JB, Wyngaarden JB, and Fredrickson DS), 2nd ed., New York, McGraw-Hill, 1966, pp429
  • 2) Brunzell JD, Deeb SS: Familial lipoprotein lipase deficiency, apoC-II deficiency and hepatic lipase deficiency. in The Metabolic and Molecular Bases of Inherited Disease (ed. by Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, and Vogelstein B), 8th ed., New York, McGraw-Hill, 2000, pp2789-2816
  • 3) Brunzell JD, Miller NE, Alaupovic P, St Hilaire RJ, Wang CS, Sarson DL, Bloom SR, Lewis B: Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity. J Lipid Res, 1983; 24: 12-19
  • 4) Kihara S, Matsuzawa Y, Kubo M, Nozaki S, Funahashi T, Yamashita S, Sho N, Tarui S: Autoimmune hyperchylomicronemia. N Engl J Med, 1989: 320; 1255-1259
  • 5) Beigneux AP, Davies BSJ, Gin P, Weinstein MM, Farber E, Qiao X, Peale F, Bunting S, Walzem RL, Wong JS, Blaner WS, Ding Z-M, Melford K, Wongsiriroj N, Shu X, de Sauvage F, Ryan RO, Fong LG, Bensadoun A, Young SG: Glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 plays a critical role in the lipolytic processing of chylomicrons. Cell Metab, 2007; 5: 279-291
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