Results 51 to 60 of about 87 (78)

Tangier disease: defective recombination of a specific Tangier apolipoprotein A-I isoform (pro-apo A-i) with high density lipoproteins. [PDF]

Proc Natl Acad Sci U S A, 1983
Schmitz G, Assmann G, Rall SC, Mahley RW.   +3 more
europepmc   +1 more source

Heterogeneity of human high density lipoprotein: presence of lipoproteins with and without apoE and their roles as substrates for lecithin:cholesterol acyltransferase reaction. [PDF]

Proc Natl Acad Sci U S A, 1980
Marcel YL, Vezina C, Emond D, Suzue G.
europepmc   +1 more source

Hypobetalipoproteinaemia--a variant of the Bassen-Kornzweig syndrome. [PDF]

Gut, 1979
Scott BB, Miller JP, Losowsky MS.
europepmc   +1 more source

Tangier disease: a structural defect in apolipoprotein A-I (apoA-I Tangier). [PDF]

Proc Natl Acad Sci U S A, 1982
Kay LL, Ronan R, Schaefer EJ, Brewer HB.
europepmc   +1 more source

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Acquired hypolipoproteinemia and hemophagocytic lymphohistiocytosis: A previously unexplored association?

Journal of Clinical Oncology, 2021
e19041 Background: Hemophagocytic lymphohistiocytosis (HLH) is a rare disease that is the result of macrophage hyperactivation, leading to disordered cellular phagocytosis that is highly fatal if left untreated. The precise precipitating factor that leads to HLH is presently unknown.
Leo Edward Reap, Vincent T Ma, Radhika Takiar, Adam Matthew Forman   +3 more
openaire   +1 more source

Wolman's disease with hypolipoproteinemia and acanthocytosis: Clinical and biochemical observations

The Journal of Pediatrics, 1970
A 9-month-old girl is described who has the characteristic findings of Wolman's disease, accompanied by malabsorption of lipid, distinctly low levels of beta lipoprotein in the serum, and acanthocytosis in peripheral blood resembling that seen in abetalipoproteinemia.
Y, Eto, T, Kitagawa
openaire   +2 more sources