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Sebastiano Calandra

Showing results (51-60 of 88) with videos related to

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Gene|October 10, 2012
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemiaLucia Magnolo, Mohamed Najah, Tatiana Fancello, et al.
Atherosclerosis|December 14, 2005
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparisonLivia Pisciotta, Claudio Priore Oliva, Giovanni Mario Pes, et al.
Atherosclerosis|August 24, 2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genesLivia Pisciotta, Laura Calabresi, Graziana Lupattelli, et al.
Atherosclerosis|May 25, 2005
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemiaEnza Di Leo, Sandra Lancellotti, Junia Y Penacchioni, et al.
Atherosclerosis|May 19, 2017
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemiaPaola Sabrina Buonuomo, Lorenzo Iughetti, Livia Pisciotta, et al.
Atherosclerosis|May 6, 2014
Lysosomal acid lipase deficiency--an under-recognized cause of dyslipidaemia and liver dysfunctionŽeljko Reiner, Ornella Guardamagna, Devaki Nair, et al.
Atherosclerosis|February 10, 2009
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindredLaura Calabresi, Peter Nilsson, Elisa Pinotti, et al.
Atherosclerosis|May 12, 2004
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemiaStefano Bertolini, Livia Pisciotta, Lilla Di Scala, et al.
Journal of Clinical Lipidology|June 30, 2019
Novel mutations of SAR1B gene in four children with chylomicron retention diseaseMaria Luisa Simone, Claudio Rabacchi, Zarife Kuloglu, et al.
Clinical Science (London, England : 1979)|June 22, 2017
Reduced platelet count, but no major platelet function abnormalities, are associated with loss-of-function ATP-binding cassette-1 gene mutationsPietro Minuz, Alessandra Meneguzzi, Eti Alessandra Femia, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Gene|October 10, 2012
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemiaLucia Magnolo, Mohamed Najah, Tatiana Fancello, et al.
Atherosclerosis|December 14, 2005
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparisonLivia Pisciotta, Claudio Priore Oliva, Giovanni Mario Pes, et al.
Atherosclerosis|August 24, 2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genesLivia Pisciotta, Laura Calabresi, Graziana Lupattelli, et al.
Atherosclerosis|May 25, 2005
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemiaEnza Di Leo, Sandra Lancellotti, Junia Y Penacchioni, et al.
Atherosclerosis|May 19, 2017
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemiaPaola Sabrina Buonuomo, Lorenzo Iughetti, Livia Pisciotta, et al.
Atherosclerosis|May 6, 2014
Lysosomal acid lipase deficiency--an under-recognized cause of dyslipidaemia and liver dysfunctionŽeljko Reiner, Ornella Guardamagna, Devaki Nair, et al.
Atherosclerosis|February 10, 2009
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindredLaura Calabresi, Peter Nilsson, Elisa Pinotti, et al.
Atherosclerosis|May 12, 2004
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemiaStefano Bertolini, Livia Pisciotta, Lilla Di Scala, et al.
Journal of Clinical Lipidology|June 30, 2019
Novel mutations of SAR1B gene in four children with chylomicron retention diseaseMaria Luisa Simone, Claudio Rabacchi, Zarife Kuloglu, et al.
Clinical Science (London, England : 1979)|June 22, 2017
Reduced platelet count, but no major platelet function abnormalities, are associated with loss-of-function ATP-binding cassette-1 gene mutationsPietro Minuz, Alessandra Meneguzzi, Eti Alessandra Femia, et al.
Pageof 9