Saada A - Search Results

1

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. Among authors: saada a. 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.

2

Lipoamide dehydrogenase activity in lymphocytes.

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

3

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. Among authors: saada ab. 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 No abstract available.

4

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: saada a. 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.

5

Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNA(leu)(UUR) gene (A3243T).

Shaag A, Saada A, Steinberg A, Navon P, Elpeleg ON. Shaag A, et al. Among authors: saada a. Biochem Biophys Res Commun. 1997 Apr 28;233(3):637-9. doi: 10.1006/bbrc.1997.6496. Biochem Biophys Res Commun. 1997. PMID: 9168904

6

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: saada a. Am J Med Genet. 1999 Jan 15;82(2):177-82. Am J Med Genet. 1999. PMID: 9934985

7

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: saada a. Biochem Biophys Res Commun. 1999 Aug 19;262(1):163-6. doi: 10.1006/bbrc.1999.1133. Biochem Biophys Res Commun. 1999. PMID: 10448086

8

ATP synthesis in lipoamide dehydrogenase deficiency.

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

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. Among authors: saada a. Am J Med Genet. 2001 Aug 1;102(2):183-7. doi: 10.1002/ajmg.1457. Am J Med Genet. 2001. PMID: 11477613

10

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA.

Mandel H, Szargel R, Labay V, Elpeleg O, Saada A, Shalata A, Anbinder Y, Berkowitz D, Hartman C, Barak M, Eriksson S, Cohen N. Mandel H, et al. Among authors: saada a. Nat Genet. 2001 Nov;29(3):337-41. doi: 10.1038/ng746. Nat Genet. 2001. PMID: 11687800

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