Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency

by Tommaso Fasano, Letizia Bocchi, Livia Pisciotta, Stefano Bertolini, Sebastiano Calandra
Published 2005-04-01

Simple detection of a point mutation in LDL receptor gene causing familial hypercholesterolemia in southern Italy by allele-specific polymerase chain reaction

by Alfredo Cantafora, Ida Blotta, Elisabetta Mercuri, Sebastiano Calandra, Stefano Bertolini
Published 1998-05-01

Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney

by Patrizia Tarugi, Giorgia Ballarini, Barbara Pinotti, Antonella Franchini, Enzo Ottaviani, Sebastiano Calandra
Published 1998-04-01

Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk

by Sebastiano Calandra, Patrizia Tarugi, Helen E. Speedy, Andrew F. Dean, Stefano Bertolini, Carol C. Shoulders
Published 2011-11-01

Analysis of two duplications of the LDL receptor gene affectingintracellular transport, catabolism, and surface binding of the LDLreceptor

by Dilip.D. Patel, Nicoletta Lelli, Rita Garuti, Salvatore Li Volti, Stefano Bertolini, Brian L. Knight, Sebastiano Calandra
Published 1998-07-01

Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene

by Patrizia Tarugi, Amedeo Lonardo, Carlo Gabelli, Franca Sala, Giorgia Ballarini, Irene Cortella, Lorenzo Previato, Stefano Bertolini, Renzo Cordera, Sebastiano Calandra
Published 2001-10-01

Lipoprotein Glomerulopathy Associated with a Mutation in Apolipoprotein E

by Riccardo Magistroni, Marco Bertolotti, Luciana Furci, Rita Adriana Fano, Marco Leonelli, Livia Pisciotta, Elisa Pellegrini, Laura Calabresi, Stefano Bertolini, Sebastiano Calandra
Published 2013-01-01

Lipoprotein Glomerulopathy Associated with a Mutation in Apolipoprotein E

by Riccardo Magistroni, Marco Bertolotti, Luciana Furci, Rita Adriana Fano, Marco Leonelli, Livia Pisciotta, Elisa Pellegrini, Laura Calabresi, Stefano Bertolini, Sebastiano Calandra
Published 2013-12-01

Niemann-Pick type C disease

by Patrizia Tarugi, Giorgia Ballarini, Bruno Bembi, Carla Battisti, Silvia Palmeri, Francesca Panzani, Enza Di Leo, Cristina Martini, Antonio Federico, Sebastiano Calandra
Published 2002-11-01

Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 +5G>C mutation in ABCA1 gene

by Serena Altilia, Livia Pisciotta, Rita Garuti, Patrizia Tarugi, Alfredo Cantafora, Laura Calabresi, Jacopo Tagliabue, Sergio Maccari, Franco Bernini, Ilaria Zanotti, Carlo Vergani, Stefano Bertolini, Sebastiano Calandra
Published 2003-02-01

Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis[S]

by Ilenia Minicocci, Sara Santini, Vito Cantisani, Nathan Stitziel, Sekar Kathiresan, Juan Antonio Arroyo, Gertrudis Martí, Livia Pisciotta, Davide Noto, Angelo B. Cefalù, Marianna Maranghi, Giancarlo Labbadia, Giovanni Pigna, Fabio Pannozzo, Fabrizio Ceci, Ester Ciociola, Stefano Bertolini, Sebastiano Calandra, Patrizia Tarugi, Maurizio Averna, Marcello Arca
Published 2013-12-01