Julie Turnbull
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 13 publications
Compassion through tele-empathy: technology-mediated symptom transference.
Journal: Future healthcare journal
Published: October 01, 2017
Lafora disease.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: October 06, 2016
Deep intronic GBE1 mutation in manifesting heterozygous patients with adult polyglucosan body disease.
Journal: JAMA neurology
Published: February 10, 2015
Mild Lafora disease: clinical, neurophysiologic, and genetic findings.
Journal: Epilepsia
Published: August 19, 2014
Deficiency of a glycogen synthase-associated protein, Epm2aip1, causes decreased glycogen synthesis and hepatic insulin resistance.
Journal: The Journal of biological chemistry
Published: October 22, 2013
PTG protein depletion rescues malin-deficient Lafora disease in mouse.
Journal: Annals of neurology
Published: August 07, 2013
Inhibiting glycogen synthesis prevents Lafora disease in a mouse model.
Journal: Annals of neurology
Published: January 25, 2013
Hyperphosphorylation of glucosyl C6 carbons and altered structure of glycogen in the neurodegenerative epilepsy Lafora disease.
Journal: Cell metabolism
Published: November 05, 2012
Early-onset Lafora body disease.
Journal: Brain : a journal of neurology
Published: September 11, 2012
Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease.
Journal: The Journal of biological chemistry
Published: June 07, 2012
Phosphorylation prevents polyglucosan transport in Lafora disease.
Journal: Neurology
Published: May 25, 2012
Last Updated: 09/26/2026