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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 8, 2024
Treatment continuity of amyotrophic lateral sclerosis with available riluzole formulations: state of the art and current challenges in a 'real-world' settingPhilippe Corcia, Nathalie Guy, Pierre-François Pradat, et al.
Expert Review of Neurotherapeutics|September 21, 2016
Management and therapeutic perspectives in amyotrophic lateral sclerosisStéphane Mathis, Philippe Couratier, Adrien Julian, et al.
Journal of the Peripheral Nervous System : JPNS|October 14, 2005
Fatigue as the main presenting symptom of chronic inflammatory demyelinating polyradiculoneuropathy: a study of 11 casesSami Boukhris, Laurent Magy, Gaël Gallouedec, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|December 2, 2005
Spirometer-dependence of vital capacity in ALS: validation of a portable device in 52 patientsPhilippe Couratier, François Vincent, Frederic Torny, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 1, 2016
Validity of medico-administrative data related to amyotrophic lateral sclerosis in France: A population-based studyRosario Vasta, Farid Boumédiene, Philippe Couratier, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 27, 2012
Juvenile and adult-onset ALS/MND among Africans: incidence, phenotype, survival: a reviewBenoit Marin, Imen Kacem, Mouhamadou Diagana, et al.
Frontiers in Neurology|September 6, 2021
Frontotemporal Pathology in Motor Neuron Disease Phenotypes: Insights From NeuroimagingMary Clare McKenna, Philippe Corcia, Philippe Couratier, et al.
Muscle & Nerve|March 28, 2003
Diagnostic value of nerve biopsy for atypical chronic inflammatory demyelinating polyneuropathy: evaluation of eight casesJean-Michel Vallat, François Tabaraud, Laurent Magy, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 6, 2017
A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALSPhilippe Corcia, Veronique Danel, Arnaud Lacour, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Prognosis of ALS: comparing data from the Limousin referral centre, France, and a Uruguayan populationJuan Gil, Maria C Vazquez, Carlos Ketzoian, et al.
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