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Volumn 27, Issue 4, 2004, Pages 256-259

Hepatic steatosis associated with heterozygotic familial hypobetalipoproteinemia;Esteatosis hepática asociada a hipobetalipoproteinemia familiar heterocigótica. Presentación de un caso

Author keywords

[No Author keywords available]

Indexed keywords

AMINOTRANSFERASE; APOLIPOPROTEIN B; CHOLESTEROL; LOW DENSITY LIPOPROTEIN; TRIACYLGLYCEROL; VERY LOW DENSITY LIPOPROTEIN;

EID: 2342507809     PISSN: 02105705     EISSN: None     Source Type: Journal    
DOI: 10.1157/13059354     Document Type: Article
Times cited : (8)

References (17)
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  • 6
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    • Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B
    • Tarugi P, Lonardo A, Ballarini G, Grisendi A, Pulvirenti M, Bagni A, et al. Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B. Gastroenterology 1996;111:1125-33.
    • (1996) Gastroenterology , vol.111 , pp. 1125-1133
    • Tarugi, P.1    Lonardo, A.2    Ballarini, G.3    Grisendi, A.4    Pulvirenti, M.5    Bagni, A.6
  • 10
    • 0036327189 scopus 로고    scopus 로고
    • Hipobetalipoproteinemia familiar. Descripción de una familia y revisión de las aportaciones españolas
    • Diego MA, Cortijo C. Hipobetalipoproteinemia familiar. Descripción de una familia y revisión de las aportaciones españolas. An Esp Pediatr 2002;56:64-7.
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    • Diego, M.A.1    Cortijo, C.2
  • 12
    • 0034019727 scopus 로고    scopus 로고
    • In vivo metabolism of apoB, apoA-1, and VLDL triglycerides in a form of hypobetalipoproteinemia not linked to the apoB gene
    • Elias N, Patterson BW, Schonfeld G. In vivo metabolism of apoB, apoA-1, and VLDL triglycerides in a form of hypobetalipoproteinemia not linked to the apoB gene. Arterioscler Thromb Vasc Biol 2000;20:1309-15.
    • (2000) Arterioscler Thromb Vasc Biol , vol.20 , pp. 1309-1315
    • Elias, N.1    Patterson, B.W.2    Schonfeld, G.3
  • 13
    • 0032898617 scopus 로고    scopus 로고
    • Known mutations of apoB account for only a small minority of hypobetalipoproteinemia
    • Jingshi W, Kim J, Li Q, Kwok PY, Cole TG, Cefalu B, et al. Known mutations of apoB account for only a small minority of hypobetalipoproteinemia. J Lipid Res 1999;40:955-9.
    • (1999) J Lipid Res , vol.40 , pp. 955-959
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    • Decreased production rates of VLDL triglycerides and apoB-100 in subjects heterozygous for familial hypobetalipoproteinemia
    • Elias N, Patterson B, Schonfeld G. Decreased production rates of VLDL triglycerides and apoB-100 in subjects heterozygous for familial hypobetalipoproteinemia. Arterioscler Thromb Vasc Biol 1999;19:2714-21.
    • (1999) Arterioscler Thromb Vasc Biol , vol.19 , pp. 2714-2721
    • Elias, N.1    Patterson, B.2    Schonfeld, G.3
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    • Familial lipoprotein deficiency (abetalipoproteinaemia, hypobetalipoproteinaemia and Tanger disease)
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    • Fredrickson DS, Gotto AM, Levy RI. Familial lipoprotein deficiency (abetalipoproteinaemia, hypobetalipoproteinaemia and Tanger disease). En: Stanburg JB, Wyngaarden JB, Fredrikson DS, editors. The metabolic basis of inherited disease. New York: McGraw Hill, 1972; p. 493-530.
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    • Fatty liver in familial hypobetalipoproteinemia: Triglyceride assembly into VLDL particles is affected by the extent of hepatic steatosis
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.