TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ... Nature genetics 40 (5), 572-574, 2008 | 1786 | 2008 |
Energy metabolism in amyotrophic lateral sclerosis L Dupuis, PF Pradat, AC Ludolph, JP Loeffler The Lancet Neurology 10 (1), 75-82, 2011 | 555 | 2011 |
Amyotrophic lateral sclerosis: an update for 2013 clinical features, pathophysiology, management and therapeutic trials PH Gordon Aging and disease 4 (5), 295, 2013 | 386 | 2013 |
EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relatives: An evidence‐based review with good … PM Andersen, GD Borasio, R Dengler, O Hardiman, K Kollewe, PN Leigh, ... European journal of neurology 12 (12), 921-938, 2005 | 358 | 2005 |
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations S Millecamps, F Salachas, C Cazeneuve, P Gordon, B Bricka, A Camuzat, ... Journal of medical genetics 47 (8), 554-560, 2010 | 346 | 2010 |
Radiation-induced neuropathy in cancer survivors S Delanian, JL Lefaix, PF Pradat Radiotherapy and Oncology 105 (3), 273-282, 2012 | 342 | 2012 |
Glutamate levels in cerebrospinal fluid in amyotrophic lateral sclerosis: a reappraisal using a new HPLC method with coulometric detection in a large cohort of patients O Spreux-Varoquaux, G Bensimon, L Lacomblez, F Salachas, PF Pradat, ... Journal of the neurological sciences 193 (2), 73-78, 2002 | 332 | 2002 |
Guidelines for preclinical animal research in ALS/MND: A consensus meeting AC Ludolph, C Bendotti, E Blaugrund, A Chio, L Greensmith, JP Loeffler, ... Amyotrophic Lateral Sclerosis 11 (1-2), 38-45, 2010 | 330 | 2010 |
Good practice in the management of amyotrophic lateral sclerosis: Clinical guidelines. An evidence‐based review with good practice points. EALSC Working Group PM Andersen, GD Borasio, R Dengler, O Hardiman, K Kollewe, PN Leigh, ... Amyotrophic lateral sclerosis 8 (4), 195-213, 2007 | 294 | 2007 |
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology E Teyssou, T Takeda, V Lebon, S Boillée, B Doukouré, G Bataillon, ... Acta neuropathologica 125, 511-522, 2013 | 266 | 2013 |
Demyelination and degeneration in the injured human spinal cord detected with diffusion and magnetization transfer MRI J Cohen-Adad, MM El Mendili, S Lehéricy, PF Pradat, S Blancho, ... Neuroimage 55 (3), 1024-1033, 2011 | 263 | 2011 |
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes S Millecamps, S Boillée, I Le Ber, D Seilhean, E Teyssou, M Giraudeau, ... Journal of medical genetics 49 (4), 258-263, 2012 | 217 | 2012 |
Causes of death in a post‐mortem series of ALS patients P Corcia, PF Pradat, F Salachas, G Bruneteau, N Le Forestier, D Seilhean, ... Amyotrophic Lateral Sclerosis 9 (1), 59-62, 2008 | 211 | 2008 |
Nogo provides a molecular marker for diagnosis of amyotrophic lateral sclerosis L Dupuis, JLG de Aguilar, F di Scala, F Rene, M de Tapia, PF Pradat, ... Neurobiology of disease 10 (3), 358-365, 2002 | 202 | 2002 |
Impaired glucose tolerance in patients with amyotrophic lateral sclerosis PF Pradat, G Bruneteau, PH Gordon, L Dupuis, D Bonnefont-Rousselot, ... Amyotrophic Lateral Sclerosis 11 (1-2), 166-171, 2010 | 193 | 2010 |
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature N Le Forestier, T Maisonobe, A Piquard, S Rivaud, L Crevier-Buchman, ... Brain 124 (10), 1989-1999, 2001 | 193 | 2001 |
Diffusion tensor imaging and voxel based morphometry study in amyotrophic lateral sclerosis: relationships with motor disability L Thivard, PF Pradat, S Lehéricy, L Lacomblez, D Dormont, J Chiras, ... Journal of Neurology, Neurosurgery & Psychiatry 78 (8), 889-892, 2007 | 179 | 2007 |
Mutations in FUS cause FALS and SALS in French and French Canadian populations VV Belzil, PN Valdmanis, PA Dion, H Daoud, E Kabashi, A Noreau, ... Neurology 73 (15), 1176-1179, 2009 | 178 | 2009 |
A large-scale multicentre cerebral diffusion tensor imaging study in amyotrophic lateral sclerosis HP Müller, MR Turner, J Grosskreutz, S Abrahams, P Bede, V Govind, ... Journal of Neurology, Neurosurgery & Psychiatry 87 (6), 570-579, 2016 | 163 | 2016 |
Up‐regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis L Dupuis, F di Scala, F Rene, M de Tapia, H Oudart, PF Pradat, ... The FASEB journal 17 (14), 1-19, 2003 | 155 | 2003 |