V. Barash

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Mycoplasma fermentans glycolipid triggers inflammatory response in rat astrocytes

S. Rottem, M. Tarshis, T. Brenner, 1998, Brain Research.

Regulation of glycogen synthetase and phosphorylase phosphatase activities in rat adipose tissue.

A. Gutman, V. Barash, H. Schramm, 1977, Biochimica et biophysica acta.

Mechanism of placental glycogen deposition in diabetes in the rat

E. Shafrir, A. Gutman, V. Barash, 2004, Diabetologia.

Regulation of Adipose Tissue Glycogen Synthetase Activation

A. Gutman, V. Barash, M. Avni, 1976 .

Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings

R. Schiffmann, R. Levy, A. Durr, 2012, Annals of neurology.

Propionic acidemia--biochemical studies.

O. Elpeleg, S. Gottfried, A. Gutman, 1989, Israel journal of medical sciences.

Solubilization of mycoplasma membranes by the nonionic detergent Triton X‐100

S. Razin, V. Barash, 1969, FEBS letters.

Placental function in maternal-fetal fat transport in diabetes.

E. Shafrir, V. Barash, E. Shafrir,, 1987, Biology of the neonate.

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

O. Elpeleg, C. Jakobs, R. Shalev, 1992, The Journal of pediatrics.

Autosomal recessive lethal infantile cytochrome C oxidase deficiency.

S. Dimauro, E. Lahat, J. Barr, 1991, American journal of diseases of children.

Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329 Ser mutation in the glycogen‐branching enzyme gene

Z. Meiner, V. Meiner, O. Abramsky, 1998, Annals of neurology.

Localization of glycogen in the placenta of diabetic rats: a light and electron microscopic study.

E. Shafrir, Z. Ne'eman, V. Barash, 1987, Placenta.

Placental glycogen metabolism in diabetic pregnancy.

E. Shafrir, V. Barash, E. Shafrir,, 1991, Israel journal of medical sciences.

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

R. Reifen, E. Kerem, O. Elpeleg, 1989, European Journal of Pediatrics.

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

H. Mandel, S. Korman, N. Bashan, 1997, American journal of medical genetics.

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

S. Korman, M. Patel, Y. Hong, 2003, Journal of Inherited Metabolic Disease.

Reduced body fat and increased hepatic lipid synthesis in mice bearing interleukin-6-secreting tumor.

O. Pappo, S. Metzger, V. Barash, 2001, American journal of physiology. Endocrinology and metabolism.

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

E. Kerem, O. Elpeleg, D. Branski, 1989, Progress in clinical and biological research.

Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients

M. Gomori, O. Abramsky, D. Soffer, 1991, Annals of neurology.

Cytosolic fatty acid binding proteins in rat placenta.

V. Barash, R. Brandes, R. Arad, 1987, Placenta.

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

S. Polak‐Charcon, E. Leshinsky‐Silver, D. Lev, 2003, Molecular genetics and metabolism.

Kinetic and immunologic evidence for the absence of glucose-6-phosphatase in early human chorionic villi and term placenta.

E. Shafrir, I. Waddell, A. Riskin, 1991, Biochimica et biophysica acta.

Incorporation of [14C]Glucose into α-1,4 Bonds of Glycogen by Leukocytes and Fibroblasts of Patients with Type III Glycogen Storage Disease

R. Deckelbaum, G. Kohn, A. Gutman, 1985, Pediatric Research.

Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency

Z. Argov, V. Barash, S. Lilling, 1991, Journal of Inherited Metabolic Disease.

Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levels.

E. Shiloni, O. Drize, S. Metzger, 1997, The American journal of physiology.

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

Y. Anikster, A. Shaag, O. Elpeleg, 1994, American journal of human genetics.

MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder

E. Leshinsky‐Silver, D. Lev, M. Sadeh, 2002, European Journal of Human Genetics.

Fructose-1,6-diphosphatase deficiency: a 20-year follow-up.

O. Elpeleg, D. Branski, H. Hurvitz, 1989, American journal of diseases of children.

Ring 18 chromosome with mental retardation, hemidysmorphism, and mitochondrial encephalomyopathy.

G. Kohn, A. Gutman, V. Barash, 1988, Pediatric neurology.

Congenital lactic acidosis associated with pyruvate carboxylase deficiency.

B. Cohen, M. Sagy, Z. Barzilay, 1981, Israel journal of medical sciences.

Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression.

E. Shahar, V. Barash, Aliza Gutman, 1988, Journal of Neurology Neurosurgery & Psychiatry.

Familial Mitochondrial Intestinal Pseudo-Obstruction and Neurogenic Bladder

D. Lev, T. Lerman-Sagie, Y. Bujanover, 2000, Journal of child neurology.

Glycogen storage disease type II in Israel.

N. Bashan, R. Potashnik, A. Gutman, 1988, Israel journal of medical sciences.

CORRECTION BY BROMOCRIPTINE OF HYPOTHALAMIC DYSFUNCTION AND POST‐PRANDIAL HYPOGLYCAEMIC SYMPTOMS IN A 31‐YEAR‐OLD WOMAN

A. Gutman, R. Siegel, J. Levy, 1983, Clinical endocrinology.

Late‐onset muscular weakness in phosphofructokinase deficiency due to exon 5/intron 5 junction point mutation

N. Raben, D. Soffer, Z. Argov, 1994, Neurology.