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M Barbagallo

Showing results (181-190 of 232) with videos related to

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Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|October 12, 2005
Family history, diabetes and extension of coronary atherosclerosis are strong predictors of adverse events after PTCA: A one-year follow-up studyManfredi Rizzo, Carlo M Barbagallo, Davide Noto, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 22, 2003
Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second alleleM Rolleri, N Vivona, G Emmanuele, et al.
Clinical and Experimental Medicine|December 4, 2003
The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarctionM T Longobardo, A B Cefalù, F Pezzino, et al.
Journal of Clinical Lipidology|May 19, 2022
Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjectsAngelo B Cefalù, Rossella Spina, Davide Noto, et al.
Atherosclerosis|October 1, 2019
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro studyVincenza Valenti, Davide Noto, Antonina Giammanco, et al.
Atherosclerosis|January 22, 2003
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH geneC M Barbagallo, G Emmanuele, A B Cefalù, et al.
Aging Cell|October 2, 2012
Tyr682 in the Aβ-precursor protein intracellular domain regulates synaptic connectivity, cholinergic function, and cognitive performanceCarmela Matrone, Siro Luvisetto, Luca R La Rosa, et al.
Clinical and Experimental Medicine|February 9, 2002
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patientsA B Cefalù, C M Barbagallo, E Sesti, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|July 21, 2011
[Malnutrition in the elderly: clinical features, psychological and social determinants. Preliminary results]A Morrone, L M Donini, P Scardella, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 12, 2002
Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemiaA B Cefalù, G Emmanuele, G Marino, et al.
Pageof 24

Showing results (181-190 of 232) with videos related to

Sort By:
Pageof 24
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|October 12, 2005
Family history, diabetes and extension of coronary atherosclerosis are strong predictors of adverse events after PTCA: A one-year follow-up studyManfredi Rizzo, Carlo M Barbagallo, Davide Noto, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 22, 2003
Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second alleleM Rolleri, N Vivona, G Emmanuele, et al.
Clinical and Experimental Medicine|December 4, 2003
The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarctionM T Longobardo, A B Cefalù, F Pezzino, et al.
Journal of Clinical Lipidology|May 19, 2022
Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjectsAngelo B Cefalù, Rossella Spina, Davide Noto, et al.
Atherosclerosis|October 1, 2019
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro studyVincenza Valenti, Davide Noto, Antonina Giammanco, et al.
Atherosclerosis|January 22, 2003
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH geneC M Barbagallo, G Emmanuele, A B Cefalù, et al.
Aging Cell|October 2, 2012
Tyr682 in the Aβ-precursor protein intracellular domain regulates synaptic connectivity, cholinergic function, and cognitive performanceCarmela Matrone, Siro Luvisetto, Luca R La Rosa, et al.
Clinical and Experimental Medicine|February 9, 2002
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patientsA B Cefalù, C M Barbagallo, E Sesti, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|July 21, 2011
[Malnutrition in the elderly: clinical features, psychological and social determinants. Preliminary results]A Morrone, L M Donini, P Scardella, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 12, 2002
Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemiaA B Cefalù, G Emmanuele, G Marino, et al.
Pageof 24