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Results:
1-13
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Results: 13
Authors:
Berger, I
Shaag, A
Anikster, Y
Baumgartner, ER
Bar-Meir, M
Joseph, A
Elpeleg, ON
Citation: I. Berger et al., Mutation analysis of the MCM gene in Israeli patients with mut(0) disease, MOL GEN MET, 73(1), 2001, pp. 107-110
Authors:
Mandel, H
Hartman, C
Berkowitz, D
Elpeleg, ON
Manov, I
Iancu, TC
Citation: H. Mandel et al., The hepatic mitochondrial DNA depletion syndrome: Ultrastructural changes in liver biopsies, HEPATOLOGY, 34(4), 2001, pp. 776-784
Authors:
Elpeleg, ON
Hammerman, C
Saada, A
Shaag, A
Golzand, E
Hochner-Celnikier, D
Berger, I
Nadjari, M
Citation: On. Elpeleg et al., Antenatal presentation of carnitine palmitoyltransferase II deficiency, AM J MED G, 102(2), 2001, pp. 183-187
Authors:
Elpeleg, ON
Korman, SH
Citation: On. Elpeleg et Sh. Korman, Sustained oral lysine supplementation in ornithine delta-aminotransferase deficiency, J INH MET D, 24(3), 2001, pp. 423-424
Authors:
Hurvitz, H
Klar, A
Korn-Lubetzki, I
Wanders, RJA
Elpeleg, ON
Citation: H. Hurvitz et al., Muscular carnitine palmitoyltransferase II deficiency in infancy, PED NEUROL, 22(2), 2000, pp. 148-150
Authors:
Saada, A
Aptowitzer, I
Link, G
Elpeleg, ON
Citation: A. Saada et al., ATP synthesis in lipoamide dehydrogenase deficiency, BIOC BIOP R, 269(2), 2000, pp. 382-386
Authors:
Lerman-Sagie, T
Houri, S
Haftel, L
Elpeleg, ON
Citation: T. Lerman-sagie et al., Mitochondrial DNA mutations are where to look, J CHILD NEU, 14(7), 1999, pp. 479-479
Authors:
Elpeleg, ON
Citation: On. Elpeleg, The molecular background of glycogen metabolism disorders, J PED END M, 12(3), 1999, pp. 363-379
Authors:
Shaag, A
Saada, A
Berger, I
Mandel, H
Joseph, A
Feigenbaum, A
Elpeleg, ON
Citation: A. Shaag et al., Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews, AM J MED G, 82(2), 1999, pp. 177-182
Authors:
Elpeleg, ON
Shaag, A
Citation: On. Elpeleg et A. Shaag, The spectrum of mutations of the aspartoacylase gene in Canavan disease innon-Jewish patients, J INH MET D, 22(4), 1999, pp. 531-534
Authors:
Besley, GTN
Elpeleg, ON
Shaag, A
Manning, NJ
Jakobs, C
Walter, JH
Citation: Gtn. Besley et al., Prenatal diagnosis of Canavan disease - Problems and dilemmas, J INH MET D, 22(3), 1999, pp. 263-266
Authors:
Chowers, I
Lerman-Sagie, T
Elpeleg, ON
Shaag, A
Merin, S
Citation: I. Chowers et al., Cone and rod dysfunction in the NARP syndrome, BR J OPHTH, 83(2), 1999, pp. 190-193
Authors:
Shany, E
Saada, A
Landau, D
Shaag, A
Hershkovitz, E
Elpeleg, ON
Citation: E. Shany et al., Lipoamide dehydrogenase deficiency due to a novel mutation in the interface domain, BIOC BIOP R, 262(1), 1999, pp. 163-166
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1-13
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