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The Pan African Medical Journal|May 17, 2021
Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report)Fatima Zahra Bouzid, Maria Mansouri, Chaikhy Abdelaziz, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 6, 2021
Amyotrophic lateral sclerosis associated with a pathological expansion in the <i>ATXN7</i> geneFlorent Cluse, Emilien Bernard, Isabelle Strubi-Vuillaume, et al.
Annals of Clinical Biochemistry|April 26, 2015
Gentle blood aspiration and tube cushioning reduce pneumatic tube system interference in lactate dehydrogenase assaysIsabelle Strubi-Vuillaume, Valentine Carlier, Catherine Obeuf, et al.
Parkinsonism & Related Disorders|September 27, 2017
Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsyVincent Huin, Isabelle Strubi-Vuillaume, Kathy Dujardin, et al.
Brain : a Journal of Neurology|July 30, 2014
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairmentJérôme Delplanque, David Devos, Vincent Huin, et al.
Antioxidants & Redox Signaling|November 21, 2013
Targeting chelatable iron as a therapeutic modality in Parkinson's diseaseDavid Devos, Caroline Moreau, Jean Christophe Devedjian, et al.
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