Elpeleg O - Search Results

1

Propionic acidemia--biochemical studies.

Barash V, Elpeleg O, Amit R, Gottfried S, Yatziv S, Gutman A. Barash V, et al. Among authors: elpeleg o. Isr J Med Sci. 1989 Feb;25(2):103-6. Isr J Med Sci. 1989. PMID: 2495260

2

A radiometric assay for aspartoacylase activity in human fibroblasts: application for the diagnosis of Canavan's disease.

Barash V, Flhor D, Morag B, Boneh A, Elpeleg ON, Gilon C. Barash V, et al. Among authors: elpeleg on. Clin Chim Acta. 1991 Sep 30;201(3):175-81. doi: 10.1016/0009-8981(91)90368-m. Clin Chim Acta. 1991. PMID: 1756590

3

Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency.

Elpeleg ON, Havkin S, Barash V, Jakobs C, Glick B, Shalev RS. Elpeleg ON, et al. J Pediatr. 1992 Sep;121(3):407-10. doi: 10.1016/s0022-3476(05)81796-2. J Pediatr. 1992. PMID: 1517917

4

Hypocarnitinemia in lysinuric protein intolerance.

Korman SH, Raas-Rothschild A, Elpeleg O, Gutman A. Korman SH, et al. Among authors: elpeleg o. Mol Genet Metab. 2002 May;76(1):81-3. doi: 10.1016/s1096-7192(02)00019-7. Mol Genet Metab. 2002. PMID: 12175786

5

Mitochondrial myopathy, Fanconi syndrome with impaired glycogen and galactose metabolism.

Hurvitz H, Kerem E, Elpeleg ON, Barash V, Klar A, Mor C, Branski D. Hurvitz H, et al. Among authors: elpeleg on. Prog Clin Biol Res. 1989;306:143-8. Prog Clin Biol Res. 1989. PMID: 2740408 No abstract available.

6

Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome.

Elpeleg ON, Ruitenbeek W, Jakobs C, Barash V, De Vivo DC, Amir N. Elpeleg ON, et al. J Pediatr. 1995 Jan;126(1):72-4. doi: 10.1016/s0022-3476(95)70506-6. J Pediatr. 1995. PMID: 7815230 Free article.

7

The frequency of the C854 mutation in the aspartoacylase gene in Ashkenazi Jews in Israel.

Elpeleg ON, Anikster Y, Barash V, Branski D, Shaag A. Elpeleg ON, et al. Am J Hum Genet. 1994 Aug;55(2):287-8. Am J Hum Genet. 1994. PMID: 8037206 Free PMC article.

8

Recurrent metabolic decompensation in profound carnitine palmitoyltransferase II deficiency.

Elpeleg ON, Joseph A, Branski D, Christensen E, Holme E, Demaugre F, Saudubray JM, Gutman A. Elpeleg ON, et al. J Pediatr. 1993 Jun;122(6):917-9. doi: 10.1016/s0022-3476(09)90019-1. J Pediatr. 1993. PMID: 8501570

9

Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathy.

Hurvitz H, Elpeleg ON, Barash V, Kerem E, Reifen RM, Ruitenbeek W, Mor C, Branski D. Hurvitz H, et al. Among authors: elpeleg on. Eur J Pediatr. 1989 Oct;149(1):48-51. doi: 10.1007/BF02024334. Eur J Pediatr. 1989. PMID: 2606128

10

3-Methylglutaconic aciduria with persistent metabolic acidosis and 'uncoupling episodes'.

Elpeleg ON, Meiron D, Barash V, Hurwitz Y, Tal I, Amir N. Elpeleg ON, et al. J Inherit Metab Dis. 1990;13(2):235-6. doi: 10.1007/BF01799695. J Inherit Metab Dis. 1990. PMID: 2116558 No abstract available.

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