Publications by authors named "Isabelle Strubi-Vuillaume"

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Amyotrophic lateral sclerosis associated with a pathological expansion in the gene.
Florent Cluse, Emilien Bernard, Isabelle Strubi-Vuillaume, David Devos, Kevin Mouzat

Amyotroph Lateral Scler Frontotemporal Degener· August 2022

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Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report).
Fatima Zahra Bouzid, Maria Mansouri, Chaikhy Abdelaziz, Nisrine Louhab, Sablonniere Bernard, Isabelle Strubi-Vuillaume

Pan Afr Med J· May 2021

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Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy.
Vincent Huin, Isabelle Strubi-Vuillaume, Kathy Dujardin, Marine Brion, Marie Delliaux

Parkinsonism Relat Disord· December 2017

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Writing tremor: Should we look for a TOR1A mutation?
Cécile Aerts, François Cassim, Isabelle Strubi-Vuillaume, Alain Destée, Bernard Sablonnière

J Neurol Sci· November 2017

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Gentle blood aspiration and tube cushioning reduce pneumatic tube system interference in lactate dehydrogenase assays.
Isabelle Strubi-Vuillaume, Valentine Carlier, Catherine Obeuf, Francis Vasseur, J-Claude Maury

Ann Clin Biochem· March 2016

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TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment.
Jérôme Delplanque, David Devos, Vincent Huin, Alexandre Genet, Olivier Sand, Isabelle Strubi-Vuillaume

Brain· October 2014

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Targeting chelatable iron as a therapeutic modality in Parkinson's disease.
David Devos, Caroline Moreau, Jean Christophe Devedjian, Jérome Kluza, Maud Petrault, Isabelle Strubi-Vuillaume

Antioxid Redox Signal· July 2014

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