PURPOSE: Type V hyperlipidemia (HTG V) characterized by accumulation of both
chylomicrons and VLDL results from a complex combination of genetic and environmental …

Only a few cases of type I hyperlipidemia occurring in patients with autoimmune disease
have been reported. We describe the case of a 35-yr-old woman suffering from severe type I …

Context: Sporadic hyperchylomicronemia (type V hyperlipoproteinemia) results from
complex interactions between genetic and environmental factors that often remain unknown …

Background: Anti-lipoprotein lipase antibodies have been described in rare cases of
patients with hypertriglyceridemia. However, no systematic study evaluating these …

The object of this study was to evaluate: a) Levels of adipose tissue lipoprotein lipase (T-LL)
and hepatic triglyceride lipase (H-LL) in 6 patients with familial hyperchylomicronemia from …

Lipoprotein lipase (LPL) is a member of the lipase family, and LPL is known to hydrolyze
triglyceride molecules found in lipoprotein particles. Understanding the pathogenesis of …

AMONG the hyperchylomicronemias, familial deficiencies of lipoprotein lipase (LPL) and of
apolipoprotein C-II are rare variants in which the underlying biochemical defects are …

Introduction Sustained chylomicronemia is a defect in post-prandial triglyceride
management characterized by severe hypertriglyceridemia (triglyceride> 10 mmol/L) due to …

A 41-year-old female patient with muscle dystrophy, hepatosplenomegaly and tendinous
xanthoma showed mild hypertriglyceridemia. The lipoprotein profile in blood showed …

We developed eight new antibodies against lipoprotein lipase (LPL), which included
polyclonal antibodies raised against recombinant human LPL produced by transformant …