نتایج جستجو برای: familial chylomicronemia

تعداد نتایج: 56099  

Journal: :The New England journal of medicine 1996
P Benlian J L De Gennes L Foubert H Zhang S E Gagné M Hayden

BACKGROUND Patients with lipoprotein lipase deficiency usually present with chylomicronemia in childhood. The syndrome has been considered nonatherogenic primarily because of the low levels of low-density lipoprotein (LDL) cholesterol. We prospectively evaluated patients with lipoprotein lipase deficiency for atherosclerosis. METHODS Evidence of carotid, peripheral, and coronary atheroscleros...

Journal: :Journal of lipid research 1992
M Reina J D Brunzell S S Deeb

The molecular basis of familial chylomicronemia (type I hyperlipoproteinemia), a rare autosomal recessive trait, was investigated in six unrelated individuals (five of Spanish descent and one of Northern European extraction). DNA amplification by polymerase chain reaction (PCR) followed by single strand conformation polymorphism (SSCP) analysis allowed rapid identification of the underlying mut...

2009
Michael M. Weinstein Liya Yin Yiping Tu Xuping Wang Xiaohui Wu Lawrence W. Castellani Rosemary L. Walzem Aldons J. Lusis Loren G. Fong Anne P. Beigneux Stephen G. Young

Objective—The risk of atherosclerosis in the setting of chylomicronemia has been a topic of debate. In this study, we examined susceptibility to atherosclerosis in Gpihbp1-deficient mice (Gpihbp1 / ), which manifest severe chylomicronemia as a result of defective lipolysis. Methods and Results—Gpihbp1 / mice on a chow diet have plasma triglyceride and cholesterol levels of 2812 209 and 319 27 m...

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