Cerebrotendinous xanthomatosis in the Israeli Druze: molecular genetics and phenotypic characteristics.

Por Leitersdorf, E., Safadi, R., Meiner, V., Reshef, A., Björkhem, I., Friedlander, Y., Morkos, S., Berginer, V. M.
Publicado em 1994

A nonsense mutation in the LDL receptor gene leads to familial hypercholesterolemia in the Druze sect.

Por Landsberger, D, Meiner, V, Reshef, A, Levy, Y, van der Westhuyzen, D R, Coetzee, G A, Leitersdorf, E
Publicado em 1992

Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan origin.

Por Leitersdorf, E, Reshef, A, Meiner, V, Levitzki, R, Schwartz, S P, Dann, E J, Berkman, N, Cali, J J, Klapholz, L, Berginer, V M
Publicado em 1993

A common Lithuanian mutation causing familial hypercholesterolemia in Ashkenazi Jews.

Por Meiner, V, Landsberger, D, Berkman, N, Reshef, A, Segal, P, Seftel, H C, van der Westhuyzen, D R, Jeenah, M S, Coetzee, G A, Leitersdorf, E
Publicado em 1991

Phenotypic and genetic variation in leptin as determinants of weight regain

Por 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
Publicado no Int J Obes (Lond) (2010)