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Eine Ebene nach oben |
Gruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2020
Hegele, Robert A.; Boren, Jan; Ginsberg, Henry N.; Arca, Marcello; Averna, Maurizio; Binder, Christoph J.; Calabresi, Laura; Chapman, M. John; Cuchel, Marina; Eckardstein, Arnold von; Frikke-Schmidt, Ruth; Gaudet, Daniel; Hovingh, G. Kees; Kronenberg, Florian; Luetjohann, Dieter; Parhofer, Klaus G.; Raal, Frederick J.; Ray, Kausik K.; Remaley, Alan T.; Stock, Jane K.; Stroes, Erik S.; Tokgozoglu, Lale und Catapano, Alberico L.
(2020):
Rare dyslipidaemias, from phenotype to genotype to management: a European Atherosclerosis Society task force consensus statement.
In: Lancet Diabetes & Endocrinology, Bd. 8, Nr. 1: S. 50-67
2018
D'Erasmo, Laura; Minicocci, Ilenia; Nicolucci, Antonio; Pintus, Paolo; Van Lennep, Janine E. Roeters; Masana, Luis; Mata, Pedro; Maria Sanchez-Hernandez, Rosa; Prieto-Matos, Pablo; Real, Jose T.; Ascaso, Juan F.; Esteve Lafuente, Eduardo; Pocovi, Miguel; Fuentes, Francisco J.; Muntoni, Sandro; Bertolini, Stefano; Sirtori, Cesare; Calabresi, Laura; Pavanello, Chiara; Averna, Maurizio; Cefalu, Angelo Baldassare; Noto, Davide; Pacifico, Adolfo Arturo; Pes, Giovanni Mario; Harada-Shiba, Mariko; Manzato, Enzo; Zambon, Sabina; Zambon, Alberto; Vogt, Anja; Scardapane, Marco; Sjouke, Barbara; Fellin, Renato und Arca, Marcello
(2018):
Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes.
In: Journal of the American College of Cardiology, Bd. 71, Nr. 3: S. 279-288
2017
Stroes, Erik; Moulin, Philippe; Parhofer, Klaus G.; Rebours, Vinciane; Löhr, J.-Matthias und Averna, Maurizio
(2017):
Diagnostic algorithm for familial chylomicronemia syndrome.
In: Atherosclerosis Supplements, Bd. 23: S. 1-7