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Laurent SERVAIS
Laurent SERVAIS
Verified email at paediatrics.ox.ac.uk
Title
Cited by
Cited by
Year
Nusinersen versus sham control in infantile-onset spinal muscular atrophy
RS Finkel, E Mercuri, BT Darras, AM Connolly, NL Kuntz, J Kirschner, ...
New England Journal of Medicine 377 (18), 1723-1732, 2017
19802017
Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy.
FRS Mercuri E, Darras BT, Chiriboga CA, Day JW, Campbell C, Connolly AM ...
New England Journal of Medicine 378 (7), 625-635, 2018
12352018
Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study
T Voit, H Topaloglu, V Straub, F Muntoni, N Deconinck, G Campion, ...
The Lancet Neurology 13 (10), 987-996, 2014
3732014
Anti-HMGCR autoantibodies in European patients with autoimmune necrotizing myopathies: inconstant exposure to statin
Y Allenbach, L Drouot, A Rigolet, JL Charuel, F Jouen, NB Romero, ...
Medicine 93 (3), 150-157, 2014
3132014
Risdiplam in type 1 spinal muscular atrophy
G Baranello, BT Darras, JW Day, N Deconinck, A Klein, R Masson, ...
New England Journal of Medicine 384 (10), 915-923, 2021
2982021
Sexual health care in persons with intellectual disabilities
L Servais
Mental retardation and developmental disabilities research reviews 12 (1), 48-56, 2006
2732006
Increased dystrophin production with golodirsen in patients with Duchenne muscular dystrophy
DE Frank, FJ Schnell, C Akana, SH El-Husayni, CA Desjardins, J Morgan, ...
Neurology 94 (21), e2270-e2282, 2020
2592020
Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy
C Le Guiner, L Servais, M Montus, T Larcher, B Fraysse, S Moullec, ...
Nature communications 8 (1), 16105, 2017
2282017
Development of the P erformance of the U pper L imb module for D uchenne muscular dystrophy
A Mayhew, ES Mazzone, M Eagle, T Duong, M Ash, V Decostre, ...
Developmental Medicine & Child Neurology 55 (11), 1038-1045, 2013
2252013
Clinical evidence supporting early treatment of patients with spinal muscular atrophy: current perspectives
T Dangouloff, L Servais
Therapeutics and clinical risk management, 1153-1161, 2019
1922019
Risdiplam-treated infants with type 1 spinal muscular atrophy versus historical controls
BT Darras, R Masson, M Mazurkiewicz-Bełdzińska, K Rose, H Xiong, ...
New England Journal of Medicine 385 (5), 427-435, 2021
1812021
Nusinersen treatment of spinal muscular atrophy: current knowledge and existing gaps
T Gidaro, L Servais
Developmental Medicine & Child Neurology 61 (1), 19-24, 2019
1792019
Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1
R Hourez, L Servais, D Orduz, D Gall, I Millard, A de Kerchove d'Exaerde, ...
Journal of Neuroscience 31 (33), 11795-11807, 2011
1552011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.
CN Investigators.
J Allergy Clin Immunol. 128 (2), 382-9, 2011
1532011
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial
E Mercuri, F Muntoni, G Baranello, R Masson, O Boespflug-Tanguy, ...
The Lancet Neurology 20 (10), 832-841, 2021
1462021
Prospective and longitudinal natural history study of patients with type 2 and 3 spinal muscular atrophy: baseline data NatHis-SMA study
A Chabanon, AM Seferian, A Daron, Y Péréon, C Cances, C Vuillerot, ...
PLoS One 13 (7), e0201004, 2018
1442018
Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial
KA Strauss, MA Farrar, F Muntoni, K Saito, JR Mendell, L Servais, ...
Nature medicine 28 (7), 1381-1389, 2022
1412022
Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled …
E Mercuri, N Deconinck, ES Mazzone, A Nascimento, M Oskoui, K Saito, ...
The Lancet Neurology 21 (1), 42-52, 2022
1362022
Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go
T Dangouloff, E Vrščaj, L Servais, D Osredkar, T Adoukonou, O Aryani, ...
Neuromuscular Disorders 31 (6), 574-582, 2021
1362021
Forelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients
C Le Guiner, M Montus, L Servais, Y Cherel, V Francois, JL Thibaud, ...
Molecular Therapy 22 (11), 1923-1935, 2014
1332014
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