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210 results

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Page 1
Acute infantile liver failure due to mutations in the TRMU gene.
Zeharia A, Shaag A, Pappo O, Mager-Heckel AM, Saada A, Beinat M, Karicheva O, Mandel H, Ofek N, Segel R, Marom D, Rötig A, Tarassov I, Elpeleg O. Zeharia A, et al. Among authors: saada a. Am J Hum Genet. 2009 Sep;85(3):401-7. doi: 10.1016/j.ajhg.2009.08.004. Am J Hum Genet. 2009. PMID: 19732863 Free PMC article.
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
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 Free article. No abstract available.
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.
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
210 results