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Browsing by Author Elpeleg, O.N.

Full Text	Issue Date	Title	Author(s)
	2006	Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs.	Smeitink, J.A.M.; Elpeleg, O.N.; Antonicka, H.; Diepstra, H.D.; Saada, A., et al
	1997	Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria	Elpeleg, O.N.; Saada, A.B.; Shaag, A.; Glustein, J.Z.; Ruitenbeek, W., et al
	1995	Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome	Elpeleg, O.N.; Ruitenbeek, W.; Jakobs, C.; Barash, V.; Vivo, D.C. De, et al