De Luca C

References (3)

Title : A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease - Calcaterra_2025_J.Clin.Lipidol__
Author(s) : Calcaterra I , Vitelli N , Di Taranto MD , De Luca C , Donnarumma S , Palermo V , Cardiero G , Iannuzzo G , Rendina D , Fortunato G , Di Minno M
Ref : J Clin Lipidol , : , 2025
Abstract :
PubMedSearch : Calcaterra_2025_J.Clin.Lipidol__
PubMedID: 41680013
Gene_locus related to this paper: human-LPL

Title : Genetic Assessment and Clinical Correlates in Severe Hypertriglyceridemia: A Systematic Review - De Luca_2025_Genes.(Basel)_16_
Author(s) : De Luca C , Ciciola P , D'Errico G , Di Taranto MD , Fortunato G , Gross C , Garn J , Iannuzzo G , Di Minno M , Calcaterra I
Ref : Genes (Basel) , 16 : , 2025
Abstract :
PubMedSearch : De Luca_2025_Genes.(Basel)_16_
PubMedID: 41300829

Title : PNLIPRP1 hypermethylation in exocrine pancreas links type 2 diabetes and cholesterol metabolism - Maurin_2024_Diabetes__db240215
Author(s) : Maurin L , Marselli L , Boissel M , Ning L , Boutry R , Fernandes J , Suleiman M , De Luca C , Leloire A , Pascat V , Toussaint B , Amanzougarene S , Derhourhi M , Jorns A , Lenzen S , Pattou F , Kerr-Conte J , Canouil M , Marchetti P , Bonnefond A , Froguel P , Khamis A
Ref : Diabetes , : , 2024
Abstract :
PubMedSearch : Maurin_2024_Diabetes__db240215
PubMedID: 39137110
Gene_locus related to this paper: human-PNLIPRP1