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Nature Genetics|April 1, 2008
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosisEdor Kabashi, Paul N Valdmanis, Patrick Dion, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 31, 2016
Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriersPaola Caroppo, Agnès Camuzat, Anne De Septenville, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Frontiers in Neurology|August 15, 2020
Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's DiseaseSabine Prud'hon, Samir Bekadar, Agnès Rastetter, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Impaired glucose tolerance in patients with amyotrophic lateral sclerosisPierre-Francois Pradat, Gaelle Bruneteau, Paul H Gordon, et al.
Neuro-Degenerative Diseases|September 22, 2011
Muscle gene expression is a marker of amyotrophic lateral sclerosis severityPierre-François Pradat, Odile Dubourg, Marc de Tapia, et al.
Neurobiology of Aging|January 12, 2011
Screening of OPTN in French familial amyotrophic lateral sclerosisStéphanie Millecamps, Séverine Boillée, Elodie Chabrol, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 25, 2018
The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophyGiorgia Querin, Timothée Lenglet, Rabab Debs, et al.
Annals of Neurology|February 1, 2011
The COMT Val158Met polymorphism affects the response to entacapone in Parkinson's disease: a randomized crossover clinical trialJean-Christophe Corvol, Cécilia Bonnet, Fanny Charbonnier-Beaupel, et al.
Neuromuscular Disorders : NMD|April 15, 2009
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementiaTanya Stojkovic, El Hadi Hammouda, Pascale Richard, et al.
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