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Stefano Bertolini

Showing results (81-90 of 93) with videos related to

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Atherosclerosis|March 17, 2004
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disordersLivia Pisciotta, Ian Hamilton-Craig, Patrizia Tarugi, et al.
Atherosclerosis|September 8, 2017
Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variantsLivia Pisciotta, Giulia Tozzi, Lorena Travaglini, et al.
European Journal of Clinical Investigation|May 16, 2019
Baseline hs-CRP predicts hypertension remission in metabolic syndromeFederico Carbone, Edorado Elia, Matteo Casula, et al.
European Journal of Clinical Investigation|September 12, 2020
Serum osteopontin predicts glycaemic profile improvement in metabolic syndrome: A pilot studyLara Caserza, Matteo Casula, Edorado Elia, et al.
Frontiers in Molecular Biosciences|June 27, 2022
Lipoprotein(a) Modulates Carotid Atherosclerosis in Metabolic SyndromeAnna Laura Cremonini, Andrea Pasta, Federico Carbone, et al.
Journal of Lipid Research|September 24, 2013
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysisIlenia Minicocci, Sara Santini, Vito Cantisani, et al.
Molecular Genetics and Metabolism|September 11, 2012
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiencyTommaso Fasano, Paolo Zanoni, Claudio Rabacchi, et al.
Journal of Medical Genetics|July 3, 2014
Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutationsMarta Futema, Vincent Plagnol, KaWah Li, et al.
Breast Cancer Research : BCR|October 29, 2022
Tolerability of Eribulin and correlation between polymorphisms and neuropathy in an unselected population of female patients with metastatic breast cancer: results of the multicenter, single arm, phase IV PAINTER studyNicla La Verde, Giovanna Damia, Ornella Garrone, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 5, 2005
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian familiesLaura Calabresi, Livia Pisciotta, Anna Costantin, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Atherosclerosis|March 17, 2004
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disordersLivia Pisciotta, Ian Hamilton-Craig, Patrizia Tarugi, et al.
Atherosclerosis|September 8, 2017
Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variantsLivia Pisciotta, Giulia Tozzi, Lorena Travaglini, et al.
European Journal of Clinical Investigation|May 16, 2019
Baseline hs-CRP predicts hypertension remission in metabolic syndromeFederico Carbone, Edorado Elia, Matteo Casula, et al.
European Journal of Clinical Investigation|September 12, 2020
Serum osteopontin predicts glycaemic profile improvement in metabolic syndrome: A pilot studyLara Caserza, Matteo Casula, Edorado Elia, et al.
Frontiers in Molecular Biosciences|June 27, 2022
Lipoprotein(a) Modulates Carotid Atherosclerosis in Metabolic SyndromeAnna Laura Cremonini, Andrea Pasta, Federico Carbone, et al.
Journal of Lipid Research|September 24, 2013
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysisIlenia Minicocci, Sara Santini, Vito Cantisani, et al.
Molecular Genetics and Metabolism|September 11, 2012
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiencyTommaso Fasano, Paolo Zanoni, Claudio Rabacchi, et al.
Journal of Medical Genetics|July 3, 2014
Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutationsMarta Futema, Vincent Plagnol, KaWah Li, et al.
Breast Cancer Research : BCR|October 29, 2022
Tolerability of Eribulin and correlation between polymorphisms and neuropathy in an unselected population of female patients with metastatic breast cancer: results of the multicenter, single arm, phase IV PAINTER studyNicla La Verde, Giovanna Damia, Ornella Garrone, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 5, 2005
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian familiesLaura Calabresi, Livia Pisciotta, Anna Costantin, et al.
Pageof 10