Results 131 to 140 of about 29,448 (207)

A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARα Modulator Pemafibrate. [PDF]

open access: yesJ Atheroscler Thromb
Otsuki T   +10 more
europepmc   +1 more source

Immune regulation by CD55 in chronic beryllium disease. [PDF]

open access: yesAm J Respir Cell Mol Biol
Li L   +9 more
europepmc   +1 more source

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