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Sebastiano Calandra

Showing results (1-10 of 88) with videos related to

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Current Opinion in Lipidology|March 22, 2017
Impact of rare variants in autosomal dominant hypercholesterolemia causing genesSebastiano Calandra, Patrizia Tarugi, Stefano Bertolini
Journal of Biomedical Research|May 13, 2018
Angiopoietin-like protein 3 (ANGPTL3) deficiency and familial combined hypolipidemiaPatrizia Tarugi, Stefano Bertolini, Sebastiano Calandra
Current Opinion in Lipidology|December 16, 2010
Altered mRNA splicing in lipoprotein disordersSebastiano Calandra, Patrizia Tarugi, Stefano Bertolini
Current Opinion in Lipidology|March 15, 2006
APOA5 and triglyceride metabolism, lesson from human APOA5 deficiencySebastiano Calandra, Claudio Priore Oliva, Patrizia Tarugi, et al.
Journal of Lipid Research|February 22, 2005
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiencyTommaso Fasano, Letizia Bocchi, Livia Pisciotta, et al.
Gene|September 17, 2014
The history of Autosomal Recessive Hypercholesterolemia (ARH). From clinical observations to gene identificationRenato Fellin, Marcello Arca, Giovanni Zuliani, et al.
Atherosclerosis. Supplements|October 3, 2017
The study of familial hypercholesterolemia in Italy: A narrative reviewStefano Bertolini, Livia Pisciotta, Tommaso Fasano, et al.
Journal of Clinical Lipidology|April 26, 2015
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 genePaola Sabrina Buonuomo, Andrea Bartuli, Claudio Rabacchi, et al.
Orphanet Journal of Rare Diseases|October 8, 2010
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosisHauke Schneider, Alexandra Lingesleben, Hans-Peter Vogel, et al.
Electrophoresis|November 27, 2004
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemiaAlfredo Cantafora, Ida Blotta, Elisabetta Pino, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
Current Opinion in Lipidology|March 22, 2017
Impact of rare variants in autosomal dominant hypercholesterolemia causing genesSebastiano Calandra, Patrizia Tarugi, Stefano Bertolini
Journal of Biomedical Research|May 13, 2018
Angiopoietin-like protein 3 (ANGPTL3) deficiency and familial combined hypolipidemiaPatrizia Tarugi, Stefano Bertolini, Sebastiano Calandra
Current Opinion in Lipidology|December 16, 2010
Altered mRNA splicing in lipoprotein disordersSebastiano Calandra, Patrizia Tarugi, Stefano Bertolini
Current Opinion in Lipidology|March 15, 2006
APOA5 and triglyceride metabolism, lesson from human APOA5 deficiencySebastiano Calandra, Claudio Priore Oliva, Patrizia Tarugi, et al.
Journal of Lipid Research|February 22, 2005
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiencyTommaso Fasano, Letizia Bocchi, Livia Pisciotta, et al.
Gene|September 17, 2014
The history of Autosomal Recessive Hypercholesterolemia (ARH). From clinical observations to gene identificationRenato Fellin, Marcello Arca, Giovanni Zuliani, et al.
Atherosclerosis. Supplements|October 3, 2017
The study of familial hypercholesterolemia in Italy: A narrative reviewStefano Bertolini, Livia Pisciotta, Tommaso Fasano, et al.
Journal of Clinical Lipidology|April 26, 2015
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 genePaola Sabrina Buonuomo, Andrea Bartuli, Claudio Rabacchi, et al.
Orphanet Journal of Rare Diseases|October 8, 2010
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosisHauke Schneider, Alexandra Lingesleben, Hans-Peter Vogel, et al.
Electrophoresis|November 27, 2004
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemiaAlfredo Cantafora, Ida Blotta, Elisabetta Pino, et al.
Pageof 9