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Neurourology and Urodynamics
|
August 21, 2009
Predictors of variability in urinary incontinence and overactive bladder symptoms
W F Stewart, V A Minassian, A G Hirsch, et al.
Annals of Neurology
|
April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypes
B 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 disease
Erica Tiberia, Julie Turnbull, Tony Wang, et al.
Annals of Neurology
|
August 6, 2013
Inhibiting glycogen synthesis prevents Lafora disease in a mouse model
Bartholomew 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 formation
Esther 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 disease
Julie 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 patients
Karla 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 6p22
E M Chan, D E Bulman, A D Paterson, et al.
Annals of Neurology
|
November 16, 2010
Glycogen hyperphosphorylation underlies lafora body formation
Julie Turnbull, Peixiang Wang, Jean-Marie Girard, et al.
Page
of 33
Search research articles
Search
Showing results (241-250 of 324) with videos related to
Sort By:
Page
of 33
Neurourology and Urodynamics
|
August 21, 2009
Predictors of variability in urinary incontinence and overactive bladder symptoms
W F Stewart, V A Minassian, A G Hirsch, et al.
Annals of Neurology
|
April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypes
B 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 disease
Erica Tiberia, Julie Turnbull, Tony Wang, et al.
Annals of Neurology
|
August 6, 2013
Inhibiting glycogen synthesis prevents Lafora disease in a mouse model
Bartholomew 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 formation
Esther 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 disease
Julie 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 patients
Karla 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 6p22
E M Chan, D E Bulman, A D Paterson, et al.
Annals of Neurology
|
November 16, 2010
Glycogen hyperphosphorylation underlies lafora body formation
Julie Turnbull, Peixiang Wang, Jean-Marie Girard, et al.
Page
of 33