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Sebastiano Calandra

Showing results (81-90 of 88) with videos related to

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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.
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.
Atherosclerosis|March 1, 2026
Real-world management of familial hypercholesterolemia in paediatric patients: a 3-year follow-up from the LIPIGEN registryFederica Galimberti, Maria Elena Capra, Elena Olmastroni, et al.
Nutrients|August 12, 2023
Clinical Approach in the Management of Paediatric Patients with Familial Hypercholesterolemia: A National Survey Conducted by the LIPIGEN Paediatric GroupCristina Pederiva, Marta Gazzotti, Marcello Arca, et al.
Children (Basel, Switzerland)|March 28, 2025
Diagnosis and Screening Strategies for Detection of Familial Hypercholesterolaemia in Children and Adolescents in Italy: A Survey from the LIPIGEN Paediatric GroupCristina Pederiva, Federica Galimberti, Manuela Casula, et al.
European Journal of Human Genetics : EJHG|June 12, 2014
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approachJorie Versmissen, Daniëlla M Oosterveer, Mojgan Yazdanpanah, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
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.
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.
Atherosclerosis|March 1, 2026
Real-world management of familial hypercholesterolemia in paediatric patients: a 3-year follow-up from the LIPIGEN registryFederica Galimberti, Maria Elena Capra, Elena Olmastroni, et al.
Nutrients|August 12, 2023
Clinical Approach in the Management of Paediatric Patients with Familial Hypercholesterolemia: A National Survey Conducted by the LIPIGEN Paediatric GroupCristina Pederiva, Marta Gazzotti, Marcello Arca, et al.
Children (Basel, Switzerland)|March 28, 2025
Diagnosis and Screening Strategies for Detection of Familial Hypercholesterolaemia in Children and Adolescents in Italy: A Survey from the LIPIGEN Paediatric GroupCristina Pederiva, Federica Galimberti, Manuela Casula, et al.
European Journal of Human Genetics : EJHG|June 12, 2014
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approachJorie Versmissen, Daniëlla M Oosterveer, Mojgan Yazdanpanah, et al.
Pageof 9