Chylomicronemia caused by lipoprotein lipase gene mutation related to a hyper-response of insulin secretion to glucose

Internal Medicine

Volumn 41, Issue 4, 2002, Pages 300-303

  Tanaka, Shu ^a   Tanabe, Yoshihiro ^b   Tamura, Hideki ^a   Ishii, Shinya ^a   Shuto, Yuji ^a   Kamegai, Jun ^a   Sugihara, Hitoshi ^a   Kobayashi, Masafumi ^a   Wakabayashi, Ichiji ^a   Murano, Takeyoshi ^c   Shirai, Koji ^c   Oikawa, Shinichi ^a  

^a NIPPON MEDICAL SCHOOL   (Japan)

^b Department of Internal Medicine   (Japan)

^c TOHO UNIVERSITY SAKURA MEDICAL CENTER   (Japan)

Author keywords

Chylomicron; Familial chylomicronemia; Hypertriglyceridemia; Lipoprotein lipase (LPL) deficiency

Indexed keywords

ASPARTIC ACID; CHYLOMICRON; GLUCOSE; GLUTAMINE; HEPARIN; INSULIN; LIPOPROTEIN LIPASE; TRIACYLGLYCEROL;

ADULT; ARTICLE; BODY HEIGHT; BODY MASS; BODY WEIGHT; CASE REPORT; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DISEASE SEVERITY; ENZYME ACTIVITY; GENE MUTATION; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; HYPERLIPOPROTEINEMIA TYPE 1; HYPERTRIGLYCERIDEMIA; INSULIN RELEASE; MALE; OBESITY; ORAL GLUCOSE TOLERANCE TEST;

EID: 0036254756     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.41.300     Document Type: Article

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