Pradat Pierre-francois
Pradat Pierre-francois
Sorbonne University. UPMC. INSERM. CNRS
Bestätigte E-Mail-Adresse bei psl.aphp.fr
TitelZitiert vonJahr
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, 2008
13452008
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, 2008
13452008
Energy metabolism in amyotrophic lateral sclerosis
L Dupuis, PF Pradat, AC Ludolph, JP Loeffler
The Lancet Neurology 10 (1), 75-82, 2011
3302011
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
2842005
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
2602002
Amyotrophic lateral sclerosis: an update for 2013 clinical features, pathophysiology, management and therapeutic trials
PH Gordon
Aging and disease 4 (5), 295, 2013
2552013
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
2502010
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
2422010
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
2282007
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
1852011
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
1742002
Radiation-induced neuropathy in cancer survivors
S Delanian, JL Lefaix, PF Pradat
Radiotherapy and Oncology 105 (3), 273-282, 2012
1652012
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
1452001
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
1432007
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 (4), 511-522, 2013
1412013
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
1392009
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), 2091-2093, 2003
1332003
Nogo expression in muscle correlates with amyotrophic lateral sclerosis severity
N Jokic, JL Gonzalez de Aguilar, PF Pradat, L Dupuis, A Echaniz‐Laguna, ...
Annals of neurology 57 (4), 553-556, 2005
1292005
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
1242012
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
1192008
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