Nogueira JP

References (3)

Title : Familial chylomicronemia syndrome caused by two genetic variants in the APOA5 gene: Severe hypertriglyceridemia that complicates pregnancy - Gutierrez_2025_J.Clin.Lipidol__
Author(s) : Gutierrez J , Castano P , Farina G , Berg G , Galvez JM , Nogueira JP
Ref : J Clin Lipidol , : , 2025
Abstract :
PubMedSearch : Gutierrez_2025_J.Clin.Lipidol__
PubMedID: 40023744

Title : The Ongoing Utility of lipoprotein lipase activity in diagnosing familial Chylomicronemia Syndrome - Farina_2025_Biochem.Biophys.Rep_44_102245
Author(s) : Farina G , Barchuk M , Sleiman A , Castellanos Pinedo A , Gutierrez Restrepo J , Zago V , Nogueira JP , Berg G
Ref : Biochem Biophys Rep , 44 :102245 , 2025
Abstract :
PubMedSearch : Farina_2025_Biochem.Biophys.Rep_44_102245
PubMedID: 41542171
Gene_locus related to this paper: human-LPL

Title : Epicardial Adipose Tissue Ceramides Are Related to Lipoprotein Lipase Activity in Coronary Artery Disease: Unfolding a Missing Link - Barchuk_2022_Arterioscler.Thromb.Vasc.Biol__101161ATVBAHA122317840
Author(s) : Barchuk M , Ancel P , Miksztowicz V , Doukbi E , Svilar L , Ynon D , Nogueira JP , Rubio M , Schreier L , Dutour A , Martin JC , Gaborit B , Berg G
Ref : Arterioscler Thromb Vasc Biol , :101161ATVBAHA122317840 , 2022
Abstract :
PubMedSearch : Barchuk_2022_Arterioscler.Thromb.Vasc.Biol__101161ATVBAHA122317840
PubMedID: 35708030