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Journal of Parkinson'S Disease|April 13, 2025
Conservative iron chelation for VAC14: Two-year clinical-radiological follow-upThomas Ollivier, David Devos, Gregory Kuchcinski, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Conservative Iron Chelation for NeuroferritinopathyFelix Marchand, Caroline Moreau, Gregory Kuchcinski, et al.Scientific Reports|October 5, 2017
Alternative promoter usage generates novel shorter MAPT mRNA transcripts in Alzheimer's disease and progressive supranuclear palsy brainsVincent Huin, Luc Buée, Hélène Behal, et al.BMC Neurology|September 17, 2024
Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case reportGuillaume Baille, Nicolas Geoffre, Anna Wissocq, et al.Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)|April 3, 2014
Use of dried blood spots and inductively coupled plasma mass spectrometry for multi-element determination in bloodVéronique Vacchina, Vincent Huin, Sébastien Hulo, et al.European Journal of Ophthalmology|April 13, 2024
Late-onset Kjellin syndrome: Diagnosis of SPG11 on fundus examinationVincent Brock, Anna Wissocq, Nicolas Geoffre, et al.Genetic Testing and Molecular Biomarkers|March 19, 2011
Development of a nonfluorescent multiplex semiquantitative polymerase chain reaction to confirm rearrangements detected by array-comparative genomic hybridizationVincent Huin, Nathalie Drouot, Pascal Chambon, et al.Cerebellum (London, England)|February 1, 2020
The TMEM240 Protein, Mutated in SCA21, Is Expressed in Purkinje Cells and Synaptic TerminalsMégane Homa, Anne Loyens, Sabiha Eddarkaoui, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2024
Cognitive Impairment Is Part of the Phenotype of Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (CANVAS)Kathy Dujardin, Céline Tard, Emily Diglé, et al.Revue Neurologique|March 8, 2025
Comparing high and low amyloid producers in Alzheimer's disease: An in-depth analysisMélanie Leroy, Anne Laure Aziz, Susanna Schraen, et al.Pageof 3