Novel mutations in two families with Darier's disease von Amichai, B., Karpati, M., Goldman, B., Peleg, L.

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A novel allele in the promoter region of the human serotonin transporter gene von Michaelovsky, E, Frisch, A, Rockah, R, Peleg, L, Magal, N, Shohat, M, Weizman, R

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Gender-dependent differences in biological rhythms of mice von Weigl, Y, Peleg, L, Dotan, A, Ashkenazi, I.E

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Keratin-9 gene mutation in a family with epidermolytic palmoplantar keratoderma von Amichai, B, Karpati, M, Goldman, B, Peleg, L

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A HEXA polymorphism (V436I) common to African-Americans and Ethiopian Jews von Peleg, L., Karpati, M., Baram, L., Zolotkovski, O., Goldman, B.

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Characteristics of enzymatically produced agar-starch sponges von Nussinovitch, A., Gershon, Z., Peleg, L.

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340 Enjoying learning – CF school can be fun von Rozenfeld, S, Kadosh, D, Landau, E, Blau, H, Peleg-Weiss, L, Mantin, H, Taizi, T, Mussaffi, H

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A novel mutation in the HEXA gene specific to Tay-Sachs disease carriers of Jewish Iraqi origin von Karpati, M., Peleg, L., Gazit, E., Akstein, E., Goldman, B.

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Protein electrophoretic markers in Israel: compilation of data and genetic affinities von Zoossmann-Diskin, A., Joel, A., Liron, M., Kerem, B., Shohat, M., Peleg, L.

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PP135-MON NUTRITION AUDIT AT A PEDIATRIC TERTIARY CENTER FROM ISRAEL von Hartman, C, Poraz, I, Kiri, M, Davidson, K, Peleg-Weis, L, Shamir, R

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Heat stable and urea resistant alkaline phosphatase in maternal neutrophils from normal and Down syndrome pregnancies von Peleg, L., Ries, L., Getslev, V., Lusky, A., Chaki, R., Lipitz, S., Barkai, G.

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Clinical manifestations of psychiatric patients who are carriers of Tay-Sachs: Disease possible role of psychotropic drugs von ZELNIK, N, KHAZANOV, V, SHEINKMAN, A, KARPATI, A. M, PELEG, L

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Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers von Peleg, L, Frisch, A, Goldman, B, Karpaty, M, Narinsky, R, Bronstein, S, Frydman, M

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Clinical Manifestations of Psychiatric Patients Who Are Carriers of Tay-Sachs Disease von Zelnik, N., Khazanov, V., Sheinkman, A., Karpati, A.M., Peleg, L.

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Screening for fragile X syndrome in women of reproductive age von Pesso, Rachel, Berkenstadt, Michal, Cuckle, Howard, Gak, Eva, Peleg, Lea, Frydman, Moshe, Barkai, Gad

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Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis von FRISCH, Amos, COLOMBO, Roberto, MICHAELOVSKY, Elena, KARPATI, Mazal, GOLDMAN, Boleslaw, PELEG, Leah

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A new mutation in the gene ATP2A2 causing darier's disease in a jewish family von Amichai, B, Karpati, M, Goldman, B, Peleg, L

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Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis von Drory, Vivian E., Birnbaum, Miriam, Peleg, Leah, Goldman, Boleslaw, Korczyn, Amos D.

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Circadian variation of nitric oxide synthase activity in mouse tissue von Tunçtan, Bahar, Weigl, Yuval, Dotan, Aviva, Peleg, Leah, Zengil, Hakan, Ashkenazi, Israel, Abacıoğlu, Nurettin

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Epidemiology of Terrorism-Related (TR) Injuries von Peleg, L., Aharonson-Daniel, L., Israel, T.

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