Publications by authors named "Elisa Pinotti"

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Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.
Lucia Magnolo, Mohamed Najah, Tatiana Fancello, Enza Di Leo, Elisa Pinotti

Gene· January 2013

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Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.
Davide Noto, Angelo B Cefalù, Vincenza Valenti, Francesca Fayer, Elisa Pinotti

Arterioscler Thromb Vasc Biol· March 2012

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A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred.
Laura Calabresi, Peter Nilsson, Elisa Pinotti, Monica Gomaraschi, Elda Favari

Atherosclerosis· August 2009

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Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutations.
Tatiana Fancello, Andrea Dardis, Camillo Rosano, Patrizia Tarugi, Barbara Tappino, Elisa Pinotti

Neurogenetics· July 2009

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Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia.
Angelo B Cefalù, Davide Noto, Lucia Magnolo, Elisa Pinotti, Monica Gomaraschi

Atherosclerosis· May 2009

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Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia.
Mohamed Najah, Enza Di Leo, Jelassi Awatef, Lucia Magnolo, Jgurim Imene, Elisa Pinotti

Clin Chim Acta· March 2009

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Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia.
Enza Di Leo, Lucia Magnolo, Elisa Pinotti, Scipione Martini, Irene Cortella

Mol Genet Metab· February 2009

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