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Bart P van de Warrenburg

Showing results (1-10 of 126) with videos related to

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Parkinsonism & Related Disorders|February 7, 2021
Family history as a clue to the diagnosis of orofacial movements in a 30-year-old man: Expert commentaryBart P van de Warrenburg
Movement Disorders : Official Journal of the Movement Disorder Society|April 24, 2014
Cognitive impairment in "Other" movement disorders: hidden defects and valuable cluesMark Walterfang, Bart P van de Warrenburg
Ebiomedicine|February 1, 2024
The FGF14 gene is a milestone in ataxia geneticsBart P van de Warrenburg, Erik-Jan Kamsteeg
Journal of Medical Genetics|December 29, 2018
Integrative network and brain expression analysis reveals mechanistic modules in ataxiaIlse Eidhof, Bart P van de Warrenburg, Annette Schenck
Cell|October 20, 2018
SnapShot: Biology of Genetic AtaxiasIlse Eidhof, Bart P van de Warrenburg, Annette Schenck
Movement Disorders : Official Journal of the Movement Disorder Society|January 7, 2012
Re-emergent tremor in a dystonic SWEDD caseKarlijn F de Laat, Bart P van de Warrenburg
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2011
Movement disorders in spinocerebellar ataxiasJudith van Gaalen, Paola Giunti, Bart P van de Warrenburg
The Lancet. Neurology|June 17, 2026
A potential turn of the tide in ataxia-telangiectasiaBart P van de Warrenburg, Michèl A A P Willemsen
Journal of Neurology|December 17, 2016
The clinical heterogeneity of drug-induced myoclonus: an illustrated reviewSabine Janssen, Bastiaan R Bloem, Bart P van de Warrenburg
Journal of Neurology|December 6, 2012
POLG mutation presenting with late-onset jerky torticollisAnil M Tuladhar, F J Anton Meijer, Bart P van de Warrenburg
Pageof 13

Showing results (1-10 of 126) with videos related to

Sort By:
Pageof 13
Parkinsonism & Related Disorders|February 7, 2021
Family history as a clue to the diagnosis of orofacial movements in a 30-year-old man: Expert commentaryBart P van de Warrenburg
Movement Disorders : Official Journal of the Movement Disorder Society|April 24, 2014
Cognitive impairment in "Other" movement disorders: hidden defects and valuable cluesMark Walterfang, Bart P van de Warrenburg
Ebiomedicine|February 1, 2024
The FGF14 gene is a milestone in ataxia geneticsBart P van de Warrenburg, Erik-Jan Kamsteeg
Journal of Medical Genetics|December 29, 2018
Integrative network and brain expression analysis reveals mechanistic modules in ataxiaIlse Eidhof, Bart P van de Warrenburg, Annette Schenck
Cell|October 20, 2018
SnapShot: Biology of Genetic AtaxiasIlse Eidhof, Bart P van de Warrenburg, Annette Schenck
Movement Disorders : Official Journal of the Movement Disorder Society|January 7, 2012
Re-emergent tremor in a dystonic SWEDD caseKarlijn F de Laat, Bart P van de Warrenburg
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2011
Movement disorders in spinocerebellar ataxiasJudith van Gaalen, Paola Giunti, Bart P van de Warrenburg
The Lancet. Neurology|June 17, 2026
A potential turn of the tide in ataxia-telangiectasiaBart P van de Warrenburg, Michèl A A P Willemsen
Journal of Neurology|December 17, 2016
The clinical heterogeneity of drug-induced myoclonus: an illustrated reviewSabine Janssen, Bastiaan R Bloem, Bart P van de Warrenburg
Journal of Neurology|December 6, 2012
POLG mutation presenting with late-onset jerky torticollisAnil M Tuladhar, F J Anton Meijer, Bart P van de Warrenburg
Pageof 13