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Indoor Air|August 30, 2022
Role of ventilation on the transmission of viruses in buildings, from a single zone to a multizone approachGaëlle Guyot, Sabrina Sayah, Sihem Guernouti, et al.
Experimental Psychology|November 13, 2013
Do you want to see the tree? Ignore the forest: inhibitory control during local processing: a negative priming study of local-global processingNicolas Poirel, Claire Sara Krakowski, Sabrina Sayah, et al.
European Journal of Neurology|January 6, 2025
Substantia nigra degeneration in spinocerebellar ataxia 2 and 7 using neuromelanin-sensitive imagingLydia Chougar, Giulia Coarelli, François-Xavier Lejeune, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2023
Huntington's Disease with Small CAG Repeat ExpansionsAnna Heinzmann, Sabrina Sayah, François-Xavier Lejeune, et al.
Cerebellum (London, England)|November 1, 2017
Personality and Neuropsychological Profiles in Friedreich AtaxiaSabrina Sayah, Jean-Yves Rotgé, Hélène Francisque, et al.
Neurology|August 20, 2025
Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar AtaxiasEmilien Petit, Daniel López Domínguez, Cecilia Marelli, et al.
Neurology|December 19, 2025
Sequence Variants in Small CAG Repeat Expansions of the <i>HTT</i> Gene and Disease Onset and Progression in Huntington DiseaseAnna Heinzmann, Emilien Petit, Jessica Dawson, et al.
BMJ Open|August 1, 2023
Patient-reported, health economic and psychosocial outcomes in patients with Friedreich ataxia (PROFA): protocol of an observational study using momentary data assessments via mobile health appMaresa Buchholz, Niklas Weber, Stephanie Borel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2020
Cognitive inhibition impairments in presymptomatic <i>C9orf72</i> carriersMaxime Montembeault, Sabrina Sayah, Daisy Rinaldi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
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