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Stefano Bertolini

Showing results (11-20 of 97) with videos related to

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Electrophoresis|November 13, 2003
Evaluation of RNA messengers involved in lipid trafficking of human intestinal cells by reverse-transcription polymerase chain reaction with competimer technology and microchip electrophoresisAlfredo Cantàfora, Ida Blotta, Roberto Rivabene, 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 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.
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|January 29, 2018
Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiencyMaja Di Rocco, Livia Pisciotta, Annalisa Madeo, 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.
Atherosclerosis|August 11, 2020
Long term follow-up of genetically confirmed patients with familial hypercholesterolemia treated with first and second-generation statins and then with PCSK9 monoclonal antibodiesAndrea Pasta, Anna Laura Cremonini, Elena Formisano, et al.
Biochimica Et Biophysica Acta|May 16, 2002
A "de novo" mutation of the LDL-receptor gene as the cause of familial hypercholesterolemiaLivia Pisciotta, Alfredo Cantafora, Francesco De Stefano, et al.
Atherosclerosis|September 25, 2020
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular featuresStefano Bertolini, Sebastiano Calandra, Marcello Arca, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
Electrophoresis|November 13, 2003
Evaluation of RNA messengers involved in lipid trafficking of human intestinal cells by reverse-transcription polymerase chain reaction with competimer technology and microchip electrophoresisAlfredo Cantàfora, Ida Blotta, Roberto Rivabene, 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 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.
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|January 29, 2018
Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiencyMaja Di Rocco, Livia Pisciotta, Annalisa Madeo, 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.
Atherosclerosis|August 11, 2020
Long term follow-up of genetically confirmed patients with familial hypercholesterolemia treated with first and second-generation statins and then with PCSK9 monoclonal antibodiesAndrea Pasta, Anna Laura Cremonini, Elena Formisano, et al.
Biochimica Et Biophysica Acta|May 16, 2002
A "de novo" mutation of the LDL-receptor gene as the cause of familial hypercholesterolemiaLivia Pisciotta, Alfredo Cantafora, Francesco De Stefano, et al.
Atherosclerosis|September 25, 2020
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular featuresStefano Bertolini, Sebastiano Calandra, Marcello Arca, et al.
Pageof 10