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Neurobiology of Aging|June 5, 2012
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Suzanne Lesage, Christel Condroyer, Stephan Klebe, et al.
Acta Neuropathologica|April 29, 2004
Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusionsDanielle Seilhean, Junko Takahashi, Khalid Hamid El Hachimi, et al.
Neurobiology of Aging|August 28, 2018
Mutation analysis of Parkinson's disease genes in a Russian data setAnton K Emelyanov, Tatiana S Usenko, Christelle Tesson, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
JAMA Neurology|December 18, 2013
DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypesPaola Caroppo, Isabelle Le Ber, Fabienne Clot, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Neurobiology of Aging|July 3, 2019
The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiencyDario Saracino, Leila Sellami, Fabienne Clot, et al.
JAMA Neurology|July 12, 2016
Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic ApproachLouise-Laure Mariani, Christelle Tesson, Perrine Charles, et al.
Autophagy|October 24, 2013
The TOMM machinery is a molecular switch in PINK1 and PARK2/PARKIN-dependent mitochondrial clearanceGiulia Bertolin, Rosa Ferrando-Miguel, Maxime Jacoupy, et al.
Annals of Neurology|February 22, 2026
Alternative Translation Initiation in PRKN Delays the Onset of Parkinson's Disease and Offers a Therapeutic TargetArian Hach, Katja Lohmann, Manabu Funayama, et al.
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