نتایج جستجو برای: apolipoprotein c ii deficiency

تعداد نتایج: 1699119  

Journal: :The Journal of Japan Atherosclerosis Society 1988

There are no adequate data that evaluate the safety and effectiveness of lowering triglyceride levels in infants. The authors report a neonate affected by familial hyperchylomicronemia, While being investigated for sepsis the serum sample obtained for blood counts was discovered to be lipaemic and the case was subsequently investigated for dyslipidemia. Based on this very abnormal lipid profile...

Journal: :Journal of lipid research 1985
E J Schaefer J M Ordovas S W Law G Ghiselli M L Kashyap L S Srivastava W H Heaton J J Albers W E Connor F T Lindgren

The biochemical, clinical, and genetic features were examined in the proband (homozygote) and heterozygotes (n = 17) affected with familial apolipoprotein A-I and C-III deficiency, variant II (previously described as apolipoprotein A-I absence). The proband was a 45-year-old white female with mild corneal opacification and significant three-vessel coronary artery disease (CAD), who died shortly...

Journal: :Journal of Atherosclerosis and Thrombosis 2013

Journal: :Journal of lipid research 1988
A Capurso A M Mogavero F Resta M Di Tommaso P Taverniti F Turturro M La Rosa S Marcovina A L Catapano

Recent data suggest that mutant immunoreactive forms of apolipoprotein C-II (apoC-II) can be detected in the plasma of patients with the apoC-II deficiency syndrome. We studied the possible presence of apoC-II mutants in the plasma of two patients with apoC-II deficiency by immunological means. The patients were hypertriglyceridemic, and apoC-II was undetectable in plasma as determined by radia...

Journal: :The Journal of clinical investigation 1988
S S Fojo U Beisiegel U Beil K Higuchi M Bojanovski R E Gregg H Greten H B Brewer

The DNA, RNA, and protein of apo C-II have been analyzed in a patient with apo C-II deficiency (apo C-IIHamburg). Markedly reduced levels of plasma and intrahepatic C-II apolipoprotein were demonstrated by immunoblotting and immunohistochemical analysis. Northern, slot blot, and in situ hybridization studies revealed low levels of a normal-sized apo C-II mRNA. No major rearrangement of the apo ...

Journal: :Arteriosclerosis 1984
E J Schaefer

This review assesses current knowledge of the clinical, genetic, and biochemical features of familial high density lipoprotein (HDL) deficiency syndromes. The focus is on HDL deficiency states occurring in the absence of severe hypertriglyceridemia or lecithin/cholesterol acyltransferase deficiency. Specific entities falling within this category include Tangier disease, familial HDL deficiency ...

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