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S Bertolini

Showing results (131-140 of 166) with videos related to

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Neuroscience Letters|August 26, 1999
Apolipoprotein E and alpha-1-antichymotrypsin allele polymorphism in sporadic and familial Alzheimer's diseaseF Licastro, S Pedrini, M Govoni, et al.
Human Genetics|May 1, 1994
A new missense mutation (Cys297-->Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste)N Lelli, R Garuti, P Pedrazzi, et al.
Journal of Lipid Research|July 1, 1996
Cerebrotendinous xanthomatosis caused by two new mutations of the sterol-27-hydroxylase gene that disrupt mRNA splicingR Garuti, N Lelli, M Barozzini, et al.
Minerva Pediatrica|September 30, 1985
[Blood lipid indexes and puberal development. Evaluation of 428 subjects]T de Toni, S Scarsi, E Tomagra, et al.
Journal of Lipid Research|August 1, 1994
Partial duplication of the EGF precursor homology domain of the LDL-receptor protein causing familial hypercholesterolemia (FH-Salerno)S Bertolini, D D Patel, D A Coviello, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 15, 2000
Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from SardiniaL Deiana, R Garuti, G M Pes, et al.
Archives of Virology|October 7, 2014
Serological and virological survey of hepatitis E virus in wild boar populations in northwestern Italy: detection of HEV subtypes 3e and 3fClaudio Caruso, P Modesto, S Bertolini, et al.
Clinical Nephrology|April 10, 2008
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs)P Aranda, P Valdivielso, L Pisciotta, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1995
Four novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemiaS Bertolini, R Garuti, W Lelli, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsSa Muntoni, H Wiebusch, M Jansen-Rust, et al.
Pageof 17

Showing results (131-140 of 166) with videos related to

Sort By:
Pageof 17
Neuroscience Letters|August 26, 1999
Apolipoprotein E and alpha-1-antichymotrypsin allele polymorphism in sporadic and familial Alzheimer's diseaseF Licastro, S Pedrini, M Govoni, et al.
Human Genetics|May 1, 1994
A new missense mutation (Cys297-->Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste)N Lelli, R Garuti, P Pedrazzi, et al.
Journal of Lipid Research|July 1, 1996
Cerebrotendinous xanthomatosis caused by two new mutations of the sterol-27-hydroxylase gene that disrupt mRNA splicingR Garuti, N Lelli, M Barozzini, et al.
Minerva Pediatrica|September 30, 1985
[Blood lipid indexes and puberal development. Evaluation of 428 subjects]T de Toni, S Scarsi, E Tomagra, et al.
Journal of Lipid Research|August 1, 1994
Partial duplication of the EGF precursor homology domain of the LDL-receptor protein causing familial hypercholesterolemia (FH-Salerno)S Bertolini, D D Patel, D A Coviello, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 15, 2000
Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from SardiniaL Deiana, R Garuti, G M Pes, et al.
Archives of Virology|October 7, 2014
Serological and virological survey of hepatitis E virus in wild boar populations in northwestern Italy: detection of HEV subtypes 3e and 3fClaudio Caruso, P Modesto, S Bertolini, et al.
Clinical Nephrology|April 10, 2008
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs)P Aranda, P Valdivielso, L Pisciotta, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1995
Four novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemiaS Bertolini, R Garuti, W Lelli, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsSa Muntoni, H Wiebusch, M Jansen-Rust, et al.
Pageof 17