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Neuroscience Letters|May 3, 2003
A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphismEmmanuelle Cousin, Didier Hannequin, Sylvain Ricard, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 21, 2009
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutationsMaria-João Ribeiro, Stéphane Thobois, Ebba Lohmann, et al.
Human Molecular Genetics|October 16, 2010
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's diseaseSuzanne Lesage, Mathieu Anheim, Christel Condroyer, et al.
Human Molecular Genetics|June 5, 2003
The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegenerationOlga Corti, Cornelia Hampe, Hana Koutnikova, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2008
Are parkin patients particularly suited for deep-brain stimulation?Ebba Lohmann, Marie-Laure Welter, Valérie Fraix, et al.
Human Molecular Genetics|January 11, 2019
LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's diseaseFiona Bonello, Sidi-Mohamed Hassoun, François Mouton-Liger, et al.
Plos One|May 8, 2012
A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonismSimon Edvardson, Yuval Cinnamon, Asaf Ta-Shma, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
European Journal of Human Genetics : EJHG|July 11, 2002
Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysisPatrice Verpillat, Agnès Camuzat, Didier Hannequin, et al.
Neurobiology of Aging|October 15, 2013
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypesIsabelle Le Ber, Inge Van Bortel, Gael Nicolas, et al.
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