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Shoshi Shpitzen

Showing results (1-10 of 8) with videos related to

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Journal of Alzheimer'S Disease : JAD|October 27, 2004
Apolipoprotein E genotyping: accurate, simple, high throughput method using ABI Prism SNaPshot Multiplex SystemLiat Ben-Avi, Ronen Durst, Shoshi Shpitzen, et al.
Journal of Lipid Research|June 1, 2010
On the mechanism of accumulation of cholestanol in the brain of mice with a disruption of sterol 27-hydroxylaseAnn Båvner, Marjan Shafaati, Magnus Hansson, et al.
European Journal of Human Genetics : EJHG|December 4, 2025
Reconsidering a silent variant: SGCA's role in atypical cardiomyopathySmadar Horowitz-Cederboim, Ronit Hoffman-Lipschuetz, Ronen Durst, et al.
Journal of Lipid Research|August 8, 2019
In search of a genetic explanation for LDLc variability in an FH family: common SNPs and a rare mutation in <i>MTTP</i> explain only part of LDL variability in an FH familyMichael Winther, Shoshi Shpitzen, Or Yaacov, et al.
Journal of Lipid Research|December 31, 2014
CETP genotype and changes in lipid levels in response to weight-loss diet intervention in the POUNDS LOST and DIRECT randomized trialsQibin Qi, Ronen Durst, Dan Schwarzfuchs, et al.
JAMA Neurology|February 10, 2015
Deep intronic GBE1 mutation in manifesting heterozygous patients with adult polyglucosan body diseaseH Orhan Akman, Or Kakhlon, Jorida Coku, et al.
Atherosclerosis|January 21, 2017
Molecular genetics of familial hypercholesterolemia in Israel-revisitedRonen Durst, Uche Ken Ibe, Shoshi Shpitzen, et al.
European Heart Journal Open|January 30, 2025
Characterization of LTBP2 mutation causing mitral valve prolapseShoshi Shpitzen, Haim Rosen, Ayal Ben-Zvi, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Alzheimer'S Disease : JAD|October 27, 2004
Apolipoprotein E genotyping: accurate, simple, high throughput method using ABI Prism SNaPshot Multiplex SystemLiat Ben-Avi, Ronen Durst, Shoshi Shpitzen, et al.
Journal of Lipid Research|June 1, 2010
On the mechanism of accumulation of cholestanol in the brain of mice with a disruption of sterol 27-hydroxylaseAnn Båvner, Marjan Shafaati, Magnus Hansson, et al.
European Journal of Human Genetics : EJHG|December 4, 2025
Reconsidering a silent variant: SGCA's role in atypical cardiomyopathySmadar Horowitz-Cederboim, Ronit Hoffman-Lipschuetz, Ronen Durst, et al.
Journal of Lipid Research|August 8, 2019
In search of a genetic explanation for LDLc variability in an FH family: common SNPs and a rare mutation in <i>MTTP</i> explain only part of LDL variability in an FH familyMichael Winther, Shoshi Shpitzen, Or Yaacov, et al.
Journal of Lipid Research|December 31, 2014
CETP genotype and changes in lipid levels in response to weight-loss diet intervention in the POUNDS LOST and DIRECT randomized trialsQibin Qi, Ronen Durst, Dan Schwarzfuchs, et al.
JAMA Neurology|February 10, 2015
Deep intronic GBE1 mutation in manifesting heterozygous patients with adult polyglucosan body diseaseH Orhan Akman, Or Kakhlon, Jorida Coku, et al.
Atherosclerosis|January 21, 2017
Molecular genetics of familial hypercholesterolemia in Israel-revisitedRonen Durst, Uche Ken Ibe, Shoshi Shpitzen, et al.
European Heart Journal Open|January 30, 2025
Characterization of LTBP2 mutation causing mitral valve prolapseShoshi Shpitzen, Haim Rosen, Ayal Ben-Zvi, et al.
Pageof 1