עקוב אחר
Vincent Meininger
Vincent Meininger
Professeur neurologie Universite Paris 6
אין אימייל מאומת
כותרת
צוטט על ידי
צוטט על ידי
שנה
A controlled trial of riluzole in amyotrophic lateral sclerosis
G Bensimon, L Lacomblez, V Meininger, ALS/Riluzole Study Group
New England Journal of Medicine 330 (9), 585-591, 1994
27601994
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
18472008
Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II.
L Lacomblez, G Bensimon, PN Leigh, P Guillet, V Meininger
Lancet (London, England) 347 (9013), 1425-1431, 1996
15911996
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
CH Wu, C Fallini, N Ticozzi, PJ Keagle, PC Sapp, K Piotrowska, P Lowe, ...
Nature 488 (7412), 499-503, 2012
7592012
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1267-1288, 2018
6482018
Clinical consequences of corticectomies involving the supplementary motor area in man
D Laplane, J Talairach, V Meininger, J Bancaud, JM Orgogozo
Journal of the neurological sciences 34 (3), 301-314, 1977
6381977
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
6292016
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
DA Figlewicz, A Krizus, MG Martinoli, V Meininger, M Dib, GA Rouleau, ...
Human molecular genetics 3 (10), 1757-1761, 1994
6281994
Dyslipidemia is a protective factor in amyotrophic lateral sclerosis
L Dupuis, P Corcia, A Fergani, JL Gonzalez De Aguilar, ...
Neurology 70 (13), 1004-1009, 2008
5872008
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
MA Van Es, JH Veldink, CGJ Saris, HM Blauw, PWJ van Vught, A Birve, ...
Nature genetics 41 (10), 1083-1087, 2009
4562009
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
3642010
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
3612021
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
L Benajiba, I Le Ber, A Camuzat, M Lacoste, C Thomas‐Anterion, ...
Annals of neurology 65 (4), 470-473, 2009
3612009
Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled study
JM Léger, B Chassande, L Musset, V Meininger, P Bouche, N Baumann
Brain 124 (1), 145-153, 2001
3452001
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
3442002
Sleep disorders and diaphragmatic function in patients with amyotrophic lateral sclerosis
I Arnulf, T Similowski, F Salachas, L Garma, S Mehiri, V Attali, ...
American journal of respiratory and critical care medicine 161 (3), 849-856, 2000
3212000
An analysis of extended survival in patients with amyotrophic lateral sclerosis treated with riluzole
M Riviere, V Meininger, P Zeisser, T Munsat
Archives of neurology 55 (4), 526-528, 1998
2871998
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
A Shatunov, K Mok, S Newhouse, ME Weale, B Smith, C Vance, ...
The Lancet Neurology 9 (10), 986-994, 2010
2812010
A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis
F Gros-Louis, R Larivière, G Gowing, S Laurent, W Camu, JP Bouchard, ...
Journal of Biological Chemistry 279 (44), 45951-45956, 2004
2742004
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
2732013
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מאמרים 1–20