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Gurusidheshwar M Wali

Showing results (1-10 of 9) with videos related to

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Annals of Indian Academy of Neurology|December 17, 2013
Spinocerebellar ataxia type 7: Report of an Indian familyGurusidheshwar M Wali
Movement Disorders : Official Journal of the Movement Disorder Society|April 6, 2005
Novel movement disorder of the lower lip: is it epilepsia partialis continua? Clues from a secondary caseGurusidheshwar M Wali
Movement Disorders : Official Journal of the Movement Disorder Society|March 7, 2003
Parkinsonism associated with Addison's diseaseGurusidheshwar M Wali
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2004
Asymmetrical awake bruxism associated with multiple system atrophyGurusidheshwar M Wali
Annals of Indian Academy of Neurology|October 27, 2011
Acute movement disorder with bilateral basal ganglia lesions in diabetic uremiaGurusidheshwar M Wali, Mallikarjun S Khanpet, Rajendra V Mali
Journal of Molecular Neuroscience : MN|March 27, 2019
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive DystoniaSubhajit Giri, Tufan Naiya, Shubhrajit Roy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD geneSian D Spacey, Enza-Maria Valente, Gurusidheshwar M Wali, et al.
Annals of Neurology|April 24, 2012
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsyJennifer Friedman, Emmanuel Roze, Jose E Abdenur, et al.
Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Annals of Indian Academy of Neurology|December 17, 2013
Spinocerebellar ataxia type 7: Report of an Indian familyGurusidheshwar M Wali
Movement Disorders : Official Journal of the Movement Disorder Society|April 6, 2005
Novel movement disorder of the lower lip: is it epilepsia partialis continua? Clues from a secondary caseGurusidheshwar M Wali
Movement Disorders : Official Journal of the Movement Disorder Society|March 7, 2003
Parkinsonism associated with Addison's diseaseGurusidheshwar M Wali
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2004
Asymmetrical awake bruxism associated with multiple system atrophyGurusidheshwar M Wali
Annals of Indian Academy of Neurology|October 27, 2011
Acute movement disorder with bilateral basal ganglia lesions in diabetic uremiaGurusidheshwar M Wali, Mallikarjun S Khanpet, Rajendra V Mali
Journal of Molecular Neuroscience : MN|March 27, 2019
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive DystoniaSubhajit Giri, Tufan Naiya, Shubhrajit Roy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD geneSian D Spacey, Enza-Maria Valente, Gurusidheshwar M Wali, et al.
Annals of Neurology|April 24, 2012
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsyJennifer Friedman, Emmanuel Roze, Jose E Abdenur, et al.
Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.
Pageof 1