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Results: 1-5 |
Results: 5

Authors: 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 Ben Avi, L 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
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