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Presse Medicale (Paris, France : 1983)|April 8, 2014
[Environmental factors in ALS]Raul Juntas-Morales, Nicolas Pageot, Philippe Corcia, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 26, 2011
Occurrence of eye movement disorders in motor neuron diseaseEmilie Beaufils, Philippe Corcia, Bertrand de Toffol, et al.
Neurobiology of Aging|December 16, 2011
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosisStéphanie Millecamps, Philippe Corcia, Cécile Cazeneuve, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 15, 2011
The high frequency of restless legs syndrome in patients with amyotrophic lateral sclerosisNadège Limousin, Hélène Blasco, Philippe Corcia, et al.
Muscle & Nerve|August 19, 2014
Nutritional assessment of amyotrophic lateral sclerosis in routine practice: value of weighing and bioelectrical impedance analysisVincent Roubeau, Hélène Blasco, François Maillot, et al.
The Journal of Hand Surgery Asian-Pacific Volume|February 8, 2018
Are Carpal Tunnel Syndrome and Regional Degenerative Osteoarthritis Linked? Results of a Case-Control StudyGuillaume Bacle, Emilie Marteau, Philippe Corcia, 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.
BMC Health Services Research|April 19, 2015
Coordinated care affects hospitalization and prognosis in amyotrophic lateral sclerosis: a cohort studyValérie Cordesse, Florence Sidorok, Priscilla Schimmel, et al.
European Journal of Neurology|February 11, 2023
Time for optimism in amyotrophic lateral sclerosisPhilippe Corcia, Christian Lunetta, Patrick Vourc'h, et al.
Journal of Medical Genetics|June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlationsStéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.
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