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V Barash

Showing results (51-60 of 56) with videos related to

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Annals of Neurology|December 16, 1998
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme geneA Lossos, Z Meiner, V Barash, et al.
Journal of Child Neurology|January 21, 2000
Neurologic presentations of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.
Pediatric Cardiology|June 9, 2004
Clinical presentations of mitochondrial cardiomyopathiesD Lev, A Nissenkorn, E Leshinsky-Silver, et al.
Molecular Genetics and Metabolism|September 2, 2003
Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiencyE Leshinsky-Silver, A Levine, A Nissenkorn, et al.
American Journal of Medical Genetics|October 23, 1997
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studiesR Parvari, K J Lei, N Bashan, et al.
Journal of Inherited Metabolic Disease|February 10, 2004
Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: possible beneficial effect of vitamin therapyY S Hong, S H Korman, J Lee, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Annals of Neurology|December 16, 1998
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme geneA Lossos, Z Meiner, V Barash, et al.
Journal of Child Neurology|January 21, 2000
Neurologic presentations of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.
Pediatric Cardiology|June 9, 2004
Clinical presentations of mitochondrial cardiomyopathiesD Lev, A Nissenkorn, E Leshinsky-Silver, et al.
Molecular Genetics and Metabolism|September 2, 2003
Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiencyE Leshinsky-Silver, A Levine, A Nissenkorn, et al.
American Journal of Medical Genetics|October 23, 1997
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studiesR Parvari, K J Lei, N Bashan, et al.
Journal of Inherited Metabolic Disease|February 10, 2004
Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: possible beneficial effect of vitamin therapyY S Hong, S H Korman, J Lee, et al.
Pageof 6