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V Barash

Showing results (41-50 of 56) with videos related to

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Progress in Clinical and Biological Research|January 1, 1989
Mitochondrial myopathy, Fanconi syndrome with impaired glycogen and galactose metabolismH Hurvitz, E Kerem, O N Elpeleg, et al.
The Clinical Investigator|January 1, 1994
Metabolic effects of nicotine on human adipose tissue in organ cultureT Chajek-Shaul, G Scherer, V Barash, et al.
American Journal of Diseases of Children (1960)|June 1, 1991
Autosomal recessive lethal infantile cytochrome C oxidase deficiencyG Eshel, E Lahat, K Fried, et al.
Clinical Endocrinology|October 1, 1983
Correction by bromocriptine of hypothalamic dysfunction and post-prandial hypoglycaemic symptoms in a 31-year-old womanA P Corcos, J Weidenfeld, J Levy, et al.
The American Journal of Physiology|August 1, 1997
Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levelsS Metzger, N Goldschmidt, V Barash, et al.
Annals of Neurology|November 1, 1991
Hereditary branching enzyme dysfunction in adult polyglucosan body disease: a possible metabolic cause in two patientsA Lossos, V Barash, D Soffer, et al.
Neuropediatrics|November 1, 1989
Canavan disease and N-acetylaspartic aciduriaO N Elpeleg, N Amir, V Barash, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2007
A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletionE Leshinsky-Silver, M Michelson, S Cohen, et al.
European Journal of Pediatrics|October 1, 1989
Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathyH Hurvitz, O N Elpeleg, V Barash, et al.
Archives of Disease in Childhood|August 18, 1999
Multiple presentation of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Progress in Clinical and Biological Research|January 1, 1989
Mitochondrial myopathy, Fanconi syndrome with impaired glycogen and galactose metabolismH Hurvitz, E Kerem, O N Elpeleg, et al.
The Clinical Investigator|January 1, 1994
Metabolic effects of nicotine on human adipose tissue in organ cultureT Chajek-Shaul, G Scherer, V Barash, et al.
American Journal of Diseases of Children (1960)|June 1, 1991
Autosomal recessive lethal infantile cytochrome C oxidase deficiencyG Eshel, E Lahat, K Fried, et al.
Clinical Endocrinology|October 1, 1983
Correction by bromocriptine of hypothalamic dysfunction and post-prandial hypoglycaemic symptoms in a 31-year-old womanA P Corcos, J Weidenfeld, J Levy, et al.
The American Journal of Physiology|August 1, 1997
Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levelsS Metzger, N Goldschmidt, V Barash, et al.
Annals of Neurology|November 1, 1991
Hereditary branching enzyme dysfunction in adult polyglucosan body disease: a possible metabolic cause in two patientsA Lossos, V Barash, D Soffer, et al.
Neuropediatrics|November 1, 1989
Canavan disease and N-acetylaspartic aciduriaO N Elpeleg, N Amir, V Barash, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2007
A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletionE Leshinsky-Silver, M Michelson, S Cohen, et al.
European Journal of Pediatrics|October 1, 1989
Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathyH Hurvitz, O N Elpeleg, V Barash, et al.
Archives of Disease in Childhood|August 18, 1999
Multiple presentation of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.
Pageof 6