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A Minassian

Showing results (241-250 of 324) with videos related to

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Neurourology and Urodynamics|August 21, 2009
Predictors of variability in urinary incontinence and overactive bladder symptomsW F Stewart, V A Minassian, A G Hirsch, et al.
Annals of Neurology|April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypesB A Minassian, T M DeLorey, R W Olsen, et al.
Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
The Journal of Biological Chemistry|June 7, 2012
Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora diseaseErica Tiberia, Julie Turnbull, Tony Wang, et al.
Annals of Neurology|August 6, 2013
Inhibiting glycogen synthesis prevents Lafora disease in a mouse modelBartholomew A Pederson, Julie Turnbull, Jonathan R Epp, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 13, 2026
Lafora disease gene therapy: EPM2A but not EPM2B overexpression results in Lafora body formationEsther O Alao, Mehrnaz Sheibani, Jun Wu, et al.
Plos Genetics|May 10, 2011
PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora diseaseJulie Turnbull, Anna A DePaoli-Roach, Xiaochu Zhao, et al.
Human Mutation|December 3, 2009
KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patientsKarla P Figueroa, Natali A Minassian, Giovanni Stevanin, et al.
Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.
Annals of Neurology|November 16, 2010
Glycogen hyperphosphorylation underlies lafora body formationJulie Turnbull, Peixiang Wang, Jean-Marie Girard, et al.
Pageof 33

Showing results (241-250 of 324) with videos related to

Sort By:
Pageof 33
Neurourology and Urodynamics|August 21, 2009
Predictors of variability in urinary incontinence and overactive bladder symptomsW F Stewart, V A Minassian, A G Hirsch, et al.
Annals of Neurology|April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypesB A Minassian, T M DeLorey, R W Olsen, et al.
Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
The Journal of Biological Chemistry|June 7, 2012
Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora diseaseErica Tiberia, Julie Turnbull, Tony Wang, et al.
Annals of Neurology|August 6, 2013
Inhibiting glycogen synthesis prevents Lafora disease in a mouse modelBartholomew A Pederson, Julie Turnbull, Jonathan R Epp, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 13, 2026
Lafora disease gene therapy: EPM2A but not EPM2B overexpression results in Lafora body formationEsther O Alao, Mehrnaz Sheibani, Jun Wu, et al.
Plos Genetics|May 10, 2011
PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora diseaseJulie Turnbull, Anna A DePaoli-Roach, Xiaochu Zhao, et al.
Human Mutation|December 3, 2009
KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patientsKarla P Figueroa, Natali A Minassian, Giovanni Stevanin, et al.
Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.
Annals of Neurology|November 16, 2010
Glycogen hyperphosphorylation underlies lafora body formationJulie Turnbull, Peixiang Wang, Jean-Marie Girard, et al.
Pageof 33