Barash V - Search Results

1

Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies.

Parvari R, Lei KJ, Bashan N, Hershkovitz E, Korman SH, Barash V, Lerman-Sagie T, Mandel H, Chou JY, Moses SW. Parvari R, et al. Among authors: barash v. Am J Med Genet. 1997 Oct 31;72(3):286-90. doi: 10.1002/(sici)1096-8628(19971031)72:3<286::aid-ajmg6>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9332655

2

Glycogen storage disease type II in Israel.

Bashan N, Potashnik R, Barash V, Gutman A, Moses SW. Bashan N, et al. Among authors: barash v. Isr J Med Sci. 1988 Apr-May;24(4-5):224-7. Isr J Med Sci. 1988. PMID: 3132435

3

Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: possible beneficial effect of vitamin therapy.

Hong YS, Korman SH, Lee J, Ghoshal P, Wu Q, Barash V, Kang S, Oh S, Kwon M, Gutman A, Rachmel A, Patel MS. Hong YS, et al. Among authors: barash v. J Inherit Metab Dis. 2003;26(8):816-8. doi: 10.1023/b:boli.0000010004.12053.5b. J Inherit Metab Dis. 2003. PMID: 14765544

4

Microsomal hexose-6-phosphate and 6-phosphogluconate dehydrogenases in extrahepatic tissues: human placenta and pig kidney cortex.

Barash V, Erlich T, Bashan N. Barash V, et al. Biochem Int. 1990;20(2):267-74. Biochem Int. 1990. PMID: 2156506

5

Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladder.

Haftel LT, Lev D, Barash V, Gutman A, Bujanover Y, Lerman-Sagie T. Haftel LT, et al. Among authors: barash v. J Child Neurol. 2000 Jun;15(6):386-9. doi: 10.1177/088307380001500606. J Child Neurol. 2000. PMID: 10868781

6

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: biochemical studies and family investigation of four generations.

Barash V, Mandel H, Sella S, Geiger R. Barash V, et al. J Inherit Metab Dis. 1990;13(2):156-64. doi: 10.1007/BF01799678. J Inherit Metab Dis. 1990. PMID: 2116546

7

Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency.

Leshinsky-Silver E, Levine A, Nissenkorn A, Barash V, Perach M, Buzhaker E, Shahmurov M, Polak-Charcon S, Lev D, Lerman-Sagie T. Leshinsky-Silver E, et al. Among authors: barash v. Mol Genet Metab. 2003 Aug;79(4):288-93. doi: 10.1016/s1096-7192(03)00097-0. Mol Genet Metab. 2003. PMID: 12948744

8

A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion.

Leshinsky-Silver E, Michelson M, Cohen S, Ginsberg M, Sadeh M, Barash V, Lerman-Sagie T, Lev D. Leshinsky-Silver E, et al. Among authors: barash v. Eur J Paediatr Neurol. 2008 Jul;12(4):309-13. doi: 10.1016/j.ejpn.2007.09.005. Epub 2007 Oct 22. Eur J Paediatr Neurol. 2008. PMID: 17951082

9

Multiple presentation of mitochondrial disorders.

Nissenkorn A, Zeharia A, Lev D, Fatal-Valevski A, Barash V, Gutman A, Harel S, Lerman-Sagie T. Nissenkorn A, et al. Among authors: barash v. Arch Dis Child. 1999 Sep;81(3):209-14. doi: 10.1136/adc.81.3.209. Arch Dis Child. 1999. PMID: 10451392 Free PMC article.

10

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. Among authors: barash v. Am J Hum Genet. 1994 Aug;55(2):287-8. Am J Hum Genet. 1994. PMID: 8037206 Free PMC article.

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