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Journal of Alzheimer'S Disease : JAD|August 17, 2013
Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389RMarie-Pierre Chaunu, Vincent Deramecourt, Valérie Buée-Scherrer, et al.NPJ Parkinson'S Disease|October 17, 2025
Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel familiesGuillaume Cogan, Christelle Tesson, Lisa Welment, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometryNadya Pyatigorskaya, Michael Sharman, Jean-Christophe Corvol, et al.Archives of Neurology|May 21, 2003
Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography studyStéphane Thobois, Maria-Joao Ribeiro, Ebba Lohmann, et al.Glia|April 18, 2018
Parkin deficiency modulates NLRP3 inflammasome activation by attenuating an A20-dependent negative feedback loopFrançois Mouton-Liger, Thibault Rosazza, Julia Sepulveda-Diaz, et al.Archives of Neurology|March 14, 2012
Exonic deletions of FXN and early-onset Friedreich ataxiaMathieu Anheim, Louise-Laure Mariani, Patrick Calvas, et al.Annals of Neurology|March 5, 2005
Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohortBart P C van de Warrenburg, Harrie Hendriks, Alexandra Dürr, et al.Parkinsonism & Related Disorders|October 12, 2010
LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohortSoreya Belarbi, Nassima Hecham, Suzanne Lesage, et al.Journal of Medical Genetics|December 10, 2013
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunctionTalya Dor, Yuval Cinnamon, Laure Raymond, et al.Frontiers in Neurology|November 23, 2017
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene PanelAhmed Bouhouche, Christelle Tesson, Wafaa Regragui, et al.Pageof 50