Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Giacoma Barraco"'
Autor:
Maurizio Averna, Francesca Fayer, Davide Noto, Angelo B. Cefalù, Pin Yue, Gustav Schonfeld, Mariangela Mina, Patrizia Tarugi, Giacoma Barraco
Publikováno v:
Atherosclerosis. 216:409-413
Primary hypobetalipoproteinemia (pHBL) is characterized by plasma cholesterol levels ApoB48, and FHBL harbouring as yet unknown molecular defects. Not linked FHBL kindred are not homogeneous in terms of plasma NCS levels. NCS cannot replace genetic H
Autor:
Marcello Arca, Francesca Fayer, Mariangela Mina, Angelo B. Cefalù, Maurizio Averna, Francesco Martino, Davide Noto, Anna Montali, Eliana Martino, Giacoma Barraco
Publikováno v:
Pediatric research. 67(2)
Current guidelines strongly recommend the identification of genetic forms of hypercholesterolemia (HC) during childhood. The usefulness of non–cholesterol sterols (NCS) in the diagnosis of genetic HC has not been fully explored. Plasma NCS were mea
Autor:
Fabrizio Gianguzza, Vincenza Valenti, Massimo Libra, Gerardo D. Elisir, Salvatore Costa, Giacoma Barraco, Angelo B. Cefalù, Salvatore Travali, Luis Cuniberti, Alberto Notarbartolo, Maurizio Averna, Davide Noto, Carlo M. Barbagallo, José Pablo Werba
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Familial hypercholesterolemia (FH) is an autosomal dominant inherited disease caused by mutations in the gene coding for the low density lipoprotein receptor (LDL-R). It is characterized by a high concentration of low density lipoprotein (LDL), which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcae134a37e94b8ce5865b240dcc30e1
http://hdl.handle.net/10447/5860
http://hdl.handle.net/10447/5860