Detalhe da pesquisa
1.
Effect of familial clustering in the genetic screening of 235 French ALS families.
J Neurol Neurosurg Psychiatry
; 92(5): 479-484, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33408239
2.
Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: Supplementary evidence for a continuum.
Eur J Neurol
; 28(8): 2780-2783, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34110677
3.
Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases.
Hum Mutat
; 41(8): 1394-1406, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32419253
4.
Reply to the letter from Gazulla et al.
Eur J Neurol
; 29(1): e3-e4, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34624147
5.
CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy.
Ann Neurol
; 78(5): 831, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26095063
6.
Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: a French national survey.
Amyotroph Lateral Scler
; 12(3): 178-84, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21073397
7.
Brain computer interface with the P300 speller: Usability for disabled people with amyotrophic lateral sclerosis.
Ann Phys Rehabil Med
; 61(1): 5-11, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29024794
8.
[Management of amyotrophic lateral sclerosis]. / Prise en charge du patient atteint de sclérose latérale amyotrophique. Une dimension rééducative indispensable pour la prévention des troubles et pour l'adaptation.
Rev Prat
; 66(5): 563-570, 2016 May.
Artigo
em Francês
| MEDLINE | ID: mdl-30512584
9.
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
Nat Neurosci
; 18(5): 631-6, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25803835
10.
[Chronic sarcoid myositis]. / Myosite chronique sarcoïdosique.
Presse Med
; 32(10): 461, 2003 Mar 15.
Artigo
em Francês
| MEDLINE | ID: mdl-12733309
11.
Do patients having a decrease in SNAP amplitude during the course of MMN present with a different condition?
J Neurol
; 256(11): 1876-80, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19641982