Detalhe da pesquisa
1.
Defining SOD1 ALS natural history to guide therapeutic clinical trial design.
J Neurol Neurosurg Psychiatry
; 88(2): 99-105, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27261500
2.
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
Ann Neurol
; 77(1): 100-13, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25382069
3.
Pre-morbid type 2 diabetes mellitus is not a prognostic factor in amyotrophic lateral sclerosis.
Muscle Nerve
; 52(3): 339-43, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25900666
4.
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.
Ann Neurol
; 71(3): 407-16, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22334415
5.
Protein kinetics of superoxide dismutase-1 in familial and sporadic amyotrophic lateral sclerosis.
Ann Clin Transl Neurol
; 10(6): 1012-1024, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37119480
6.
Transplantation of human neural progenitor cells secreting GDNF into the spinal cord of patients with ALS: a phase 1/2a trial.
Nat Med
; 28(9): 1813-1822, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36064599
7.
Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation.
Amyotroph Lateral Scler
; 11(1-2): 232-6, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20184521
8.
The NEALS primary lateral sclerosis registry.
Amyotroph Lateral Scler Frontotemporal Degener
; 21(sup1): 74-81, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32915077
9.
A randomized controlled trial of resistance and endurance exercise in amyotrophic lateral sclerosis.
Amyotroph Lateral Scler Frontotemporal Degener
; 19(3-4): 250-258, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29191052
10.
Patients with ALS show highly correlated progression rates in left and right limb muscles.
Neurology
; 89(2): 196-206, 2017 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28600459
11.
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis.
Neuromuscul Disord
; 25(4): 289-96, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25617006
12.
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis.
JAMA Neurol
; 71(4): 449-53, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24535663
13.
Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis.
Neurobiol Aging
; 34(9): 2234.e13-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23597494
14.
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study.
Lancet Neurol
; 12(5): 435-42, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23541756