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Reema Paudel

Showing results (1-10 of 15) with videos related to

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Neuro-Degenerative Diseases|November 27, 2015
DYT6 Dystonia: A Neuropathological StudyReema Paudel, Abi Li, John Hardy, et al.
Journal of the Neurological Sciences|April 24, 2012
Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxiaGeorgios Koutsis, Sally Pemble, Mary G Sweeney, et al.
Cerebellum (London, England)|March 21, 2016
Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 GeneSarah Wiethoff, Conceição Bettencourt, Reema Paudel, et al.
Acta Neuropathologica Communications|November 19, 2014
Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusionsReema Paudel, Aoife Kiely, Abi Li, et al.
Neuroscience Letters|June 30, 2012
Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohortsMichael C Kruer, Reema Paudel, Wendy Wagoner, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 21, 2012
THAP1 mutations and dystonia phenotypes: genotype phenotype correlationsGeorgia Xiromerisiou, Henry Houlden, Nikolaos Scarmeas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic formsAnnu Aggarwal, Susanne A Schneider, Henry Houlden, et al.
Gene|December 24, 2013
C19orf12 mutation leads to a pallido-pyramidal syndromeMichael C Kruer, Mustafa A Salih, Catherine Mooney, et al.
Neurobiology of Aging|December 26, 2009
Mutational analysis of parkin and PINK1 in multiple system atrophyJanet A Brooks, Henry Houlden, Anna Melchers, et al.
Elife|June 9, 2015
Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neuronsSamuel S Pappas, Katherine Darr, Sandra M Holley, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Neuro-Degenerative Diseases|November 27, 2015
DYT6 Dystonia: A Neuropathological StudyReema Paudel, Abi Li, John Hardy, et al.
Journal of the Neurological Sciences|April 24, 2012
Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxiaGeorgios Koutsis, Sally Pemble, Mary G Sweeney, et al.
Cerebellum (London, England)|March 21, 2016
Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 GeneSarah Wiethoff, Conceição Bettencourt, Reema Paudel, et al.
Acta Neuropathologica Communications|November 19, 2014
Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusionsReema Paudel, Aoife Kiely, Abi Li, et al.
Neuroscience Letters|June 30, 2012
Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohortsMichael C Kruer, Reema Paudel, Wendy Wagoner, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 21, 2012
THAP1 mutations and dystonia phenotypes: genotype phenotype correlationsGeorgia Xiromerisiou, Henry Houlden, Nikolaos Scarmeas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic formsAnnu Aggarwal, Susanne A Schneider, Henry Houlden, et al.
Gene|December 24, 2013
C19orf12 mutation leads to a pallido-pyramidal syndromeMichael C Kruer, Mustafa A Salih, Catherine Mooney, et al.
Neurobiology of Aging|December 26, 2009
Mutational analysis of parkin and PINK1 in multiple system atrophyJanet A Brooks, Henry Houlden, Anna Melchers, et al.
Elife|June 9, 2015
Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neuronsSamuel S Pappas, Katherine Darr, Sandra M Holley, et al.
Pageof 2