Elpeleg ON - Search Results

1

Lipoamide dehydrogenase activity in lymphocytes.

Berger I, Elpeleg ON, Saada A. Berger I, et al. Among authors: elpeleg on. Clin Chim Acta. 1996 Dec 30;256(2):197-201. doi: 10.1016/s0009-8981(96)06420-0. Clin Chim Acta. 1996. PMID: 9027430

2

Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria.

Elpeleg ON, Saada AB, Shaag A, Glustein JZ, Ruitenbeek W, Tein I, Halevy J. Elpeleg ON, et al. Muscle Nerve. 1997 Feb;20(2):238-40. doi: 10.1002/(sici)1097-4598(199702)20:2<238::aid-mus18>3.0.co;2-z. Muscle Nerve. 1997. PMID: 9040667 Free article. No abstract available.

3

Liver disease in the Ashkenazi-Jewish lipoamide dehydrogenase deficiency.

Aptowitzer I, Saada A, Faber J, Kleid D, Elpeleg ON. Aptowitzer I, et al. Among authors: elpeleg on. J Pediatr Gastroenterol Nutr. 1997 May;24(5):599-601. doi: 10.1097/00005176-199705000-00019. J Pediatr Gastroenterol Nutr. 1997. PMID: 9161958 No abstract available.

4

Lipoamide dehydrogenase deficiency in Ashkenazi Jews: an insertion mutation in the mitochondrial leader sequence.

Elpeleg ON, Shaag A, Glustein JZ, Anikster Y, Joseph A, Saada A. Elpeleg ON, et al. Hum Mutat. 1997;10(3):256-7. doi: 10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z. Hum Mutat. 1997. PMID: 9298831 No abstract available.

5

Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews.

Shaag A, Saada A, Berger I, Mandel H, Joseph A, Feigenbaum A, Elpeleg ON. Shaag A, et al. Among authors: elpeleg on. Am J Med Genet. 1999 Jan 15;82(2):177-82. Am J Med Genet. 1999. PMID: 9934985

6

ATP synthesis in lipoamide dehydrogenase deficiency.

Saada A, Aptowitzer I, Link G, Elpeleg ON. Saada A, et al. Among authors: elpeleg on. Biochem Biophys Res Commun. 2000 Mar 16;269(2):382-6. doi: 10.1006/bbrc.2000.2310. Biochem Biophys Res Commun. 2000. PMID: 10708561

7

TAT-mediated delivery of LAD restores pyruvate dehydrogenase complex activity in the mitochondria of patients with LAD deficiency.

Rapoport M, Saada A, Elpeleg O, Lorberboum-Galski H. Rapoport M, et al. Mol Ther. 2008 Apr;16(4):691-7. doi: 10.1038/mt.2008.4. Epub 2008 Feb 5. Mol Ther. 2008. PMID: 18362926 Free article.

8

Lipoamide dehydrogenase deficiency due to a novel mutation in the interface domain.

Shany E, Saada A, Landau D, Shaag A, Hershkovitz E, Elpeleg ON. Shany E, et al. Among authors: elpeleg on. Biochem Biophys Res Commun. 1999 Aug 19;262(1):163-6. doi: 10.1006/bbrc.1999.1133. Biochem Biophys Res Commun. 1999. PMID: 10448086

9

Antenatal presentation of carnitine palmitoyltransferase II deficiency.

Elpeleg ON, Hammerman C, Saada A, Shaag A, Golzand E, Hochner-Celnikier D, Berger I, Nadjari M. Elpeleg ON, et al. Am J Med Genet. 2001 Aug 1;102(2):183-7. doi: 10.1002/ajmg.1457. Am J Med Genet. 2001. PMID: 11477613

10

mtDNA depletion myopathy: elucidation of the tissue specificity in the mitochondrial thymidine kinase (TK2) deficiency.

Saada A, Shaag A, Elpeleg O. Saada A, et al. Mol Genet Metab. 2003 May;79(1):1-5. doi: 10.1016/s1096-7192(03)00063-5. Mol Genet Metab. 2003. PMID: 12765840

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