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Shahram Attarian
Shahram Attarian
在 ap-hm.fr 的电子邮件经过验证 - 首页
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引用次数
引用次数
年份
Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis
D Adams, A Gonzalez-Duarte, WD O’Riordan, CC Yang, M Ueda, ...
New England Journal of Medicine 379 (1), 11-21, 2018
20142018
Guillain–Barré and Miller Fisher syndromes—new diagnostic classification
BR Wakerley, A Uncini, N Yuki
Nature Reviews Neurology 10 (9), 537-544, 2014
5552014
Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes
K Nguyen, G Bassez, M Krahn, R Bernard, P Laforêt, V Labelle, ...
Archives of neurology 64 (8), 1176-1182, 2007
2812007
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task …
PYK Van den Bergh, PA van Doorn, RDM Hadden, B Avau, ...
Journal of the Peripheral Nervous System 26 (3), 242-268, 2021
2722021
Regional variation of Guillain-Barré syndrome
AY Doets, C Verboon, B Van Den Berg, T Harbo, DR Cornblath, ...
Brain 141 (10), 2866-2877, 2018
2462018
Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (PATH): a randomised, double-blind, placebo-controlled, phase 3 trial
IN van Schaik, V Bril, N van Geloven, HP Hartung, RA Lewis, G Sobue, ...
The Lancet Neurology 17 (1), 35-46, 2018
2402018
Treatment of myasthenia gravis exacerbation with intravenous immunoglobulin: a randomized double-blind clinical trial
P Gajdos, C Tranchant, B Clair, F Bolgert, B Eymard, T Stojkovic, ...
Archives of neurology 62 (11), 1689-1693, 2005
2212005
MUSK, a new target for mutations causing congenital myasthenic syndrome
F Chevessier, B Faraut, A Ravel-Chapuis, P Richard, K Gaudon, ...
Human molecular genetics 13 (24), 3229-3240, 2004
1962004
Contactin 1 IgG4 associates to chronic inflammatory demyelinating polyneuropathy with sensory ataxia
Y Miura, JJ Devaux, Y Fukami, C Manso, M Belghazi, AHY Wong, N Yuki, ...
Brain 138 (6), 1484-1491, 2015
1892015
Autoantibodies to nodal isoforms of neurofascin in chronic inflammatory demyelinating polyneuropathy
E Delmont, C Manso, L Querol, A Cortese, A Berardinelli, A Lozza, ...
Brain 140 (7), 1851-1858, 2017
1822017
Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathy
J Böhm, F Chevessier, AM De Paula, C Koch, S Attarian, C Feger, ...
The American Journal of Human Genetics 92 (2), 271-278, 2013
1672013
Effect of ascorbic acid in patients with Charcot–Marie–Tooth disease type 1A: a multicentre, randomised, double-blind, placebo-controlled trial
J Micallef, S Attarian, O Dubourg, PM Gonnaud, JY Hogrel, T Stojkovic, ...
The Lancet Neurology 8 (12), 1103-1110, 2009
1512009
Disrupting the right prefrontal cortex alters moral judgement
S Tassy, O Oullier, Y Duclos, O Coulon, J Mancini, C Deruelle, S Attarian, ...
Social cognitive and affective neuroscience 7 (3), 282-288, 2012
1472012
Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial
JF Howard, V Bril, T Vu, C Karam, S Peric, T Margania, H Murai, ...
The Lancet Neurology 20 (7), 526-536, 2021
1442021
An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth …
S Attarian, JM Vallat, L Magy, B Funalot, PM Gonnaud, A Lacour, ...
Orphanet journal of rare diseases 9, 1-15, 2014
1412014
Development of a French isometric strength normative database for adults using quantitative muscle testing
JY Hogrel, CA Payan, G Ollivier, V Tanant, S Attarian, A Couillandre, ...
Archives of physical medicine and rehabilitation 88 (10), 1289-1297, 2007
1322007
Multifocal motor neuropathy with and without conduction block: a single entity?
E Delmont, JP Azulay, R Giorgi, S Attarian, A Verschueren, D Uzenot, ...
Neurology 67 (4), 592-596, 2006
1312006
A phase II− III trial of olesoxime in subjects with amyotrophic lateral sclerosis
T Lenglet, L Lacomblez, JL Abitbol, A Ludolph, JS Mora, W Robberecht, ...
European journal of neurology 21 (3), 529-536, 2014
1252014
Analysis of the DYSF mutational spectrum in a large cohort of patients
M Krahn, C Béroud, V Labelle, K Nguyen, R Bernard, G Bassez, ...
Human mutation 30 (2), E345-E375, 2009
1192009
International Guillain‐Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in …
BC Jacobs, B van den Berg, C Verboon, G Chavada, DR Cornblath, ...
Journal of the Peripheral Nervous System 22 (2), 68-76, 2017
1112017
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