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Page 1
Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.
Durst R, Colombo R, Shpitzen S, Avi LB, Friedlander Y, Wexler R, Raal FJ, Marais DA, Defesche JC, Mandelshtam MY, Kotze MJ, Leitersdorf E, Meiner V. Durst R, et al. Among authors: shpitzen s. Am J Hum Genet. 2001 May;68(5):1172-88. doi: 10.1086/320123. Epub 2001 Apr 17. Am J Hum Genet. 2001. PMID: 11309683 Free PMC article.
The discrete and combined effect of SREBP-2 and SCAP isoforms in the control of plasma lipids among familial hypercholesterolaemia patients.
Durst R, Jansen A, Erez G, Bravdo R, Butbul E, Ben Avi L, Shpitzen S, Lotan C, Leitersdorf E, Defesche J, Friedlander Y, Meiner V, Miserez AR. Durst R, et al. Among authors: shpitzen s. Atherosclerosis. 2006 Dec;189(2):443-50. doi: 10.1016/j.atherosclerosis.2006.01.001. Epub 2006 Feb 8. Atherosclerosis. 2006. PMID: 16466730
Phenotypic and genetic variation in leptin as determinants of weight regain.
Erez G, Tirosh A, Rudich A, Meiner V, Schwarzfuchs D, Sharon N, Shpitzen S, Blüher M, Stumvoll M, Thiery J, Fiedler GM, Friedlander Y, Leiterstdorf E, Shai I. Erez G, et al. Among authors: shpitzen s. Int J Obes (Lond). 2011 Jun;35(6):785-792. doi: 10.1038/ijo.2010.217. Epub 2010 Nov 2. Int J Obes (Lond). 2011. PMID: 21042325 Free PMC article. Clinical Trial.
29 results