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Meiner, V
Shpitzen, S
Mandel, H
Klar, A
Ben-Neriah, Z
Zlotogora, J
Sagi, M
Lossos, A
Bargal, R
Sury, V
Carmi, R
Leitersdorf, E
Zeigler, M
Citation: V. Meiner et al., Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C, GENET MED, 3(5), 2001, pp. 343-348
Authors:
Durst, R
Colombo, R
Shpitzen, S
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Friedlander, Y
Wexler, R
Raal, FJ
Marais, DA
Defesche, JC
Mandelshtam, MY
Kotze, MJ
Leitersdorf, E
Meiner, V
Citation: R. Durst et al., 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, AM J HU GEN, 68(5), 2001, pp. 1172-1188
Authors:
Kark, JD
Sinnreich, R
Leitersdorf, E
Friedlander, Y
Shpitzen, S
Luc, G
Citation: Jd. Kark et al., Taq1B CETP polymorphism, plasma CETP, lipoproteins, apolipoproteins and sex differences in a Jewish population sample characterized by low HDL-cholesterol, ATHEROSCLER, 151(2), 2000, pp. 509-518
Authors:
Knoblauch, H
Muller-Myhsok, B
Busjahn, A
Ben Avi, L
Bahring, S
Baron, H
Heath, SC
Uhlmann, R
Faulhaber, HD
Shpitzen, S
Aydin, A
Reshef, A
Rosenthal, M
Eliav, O
Muhl, A
Lowe, A
Schurr, D
Harats, D
Jeschke, E
Friedlander, Y
Schuster, H
Luft, FC
Leitersdorf, E
Citation: H. Knoblauch et al., A cholesterol-lowering gene maps to chromosome 13q, AM J HU GEN, 66(1), 2000, pp. 157-166
Authors:
Lossos, A
Meiner, Z
Barash, V
Soffer, D
Schlesinger, I
Abramsky, O
Argov, Z
Shpitzen, S
Meiner, V
Citation: A. Lossos et al., Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr(329)Ser mutation in the glycogen-branching enzyme gene, ANN NEUROL, 44(6), 1998, pp. 867-872