Detalhe da pesquisa
1.
Acceptance and Commitment Therapy plus usual care for improving quality of life in people with motor neuron disease (COMMEND): a multicentre, parallel, randomised controlled trial in the UK.
Lancet
; 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38735299
2.
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Nature
; 477(7363): 211-5, 2011 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21857683
3.
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2.
Proc Natl Acad Sci U S A
; 111(40): 14524-9, 2014 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25246588
4.
Wound botulism, its neurological manifestations, treatment and outcomes: A case series from the Glasgow outbreak, 2015.
Scott Med J
; 62(4): 136-141, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28480790
5.
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.
Brain
; 137(Pt 5): 1323-36, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24727571
6.
Genotype-phenotype characterisation of long survivors with motor neuron disease in Scotland.
J Neurol
; 270(3): 1702-1712, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36515702
7.
Improved survival and 30-day mortality after gastrostomy in Scottish motor neurone disease patients: evidence from a national retrospective cohort study using STROBE criteria.
Amyotroph Lateral Scler Frontotemporal Degener
; 20(3-4): 165-171, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30835562
8.
Genetic epidemiology of motor neuron disease-associated variants in the Scottish population.
Neurobiol Aging
; 51: 178.e11-178.e20, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28089114
9.
Corrigendum to "Genetic epidemiology of motor neuron disease-associated variants in the Scottish population." [Neurobiol. Aging 51 (2017) 178.e11-178.e20].
Neurobiol Aging
; 56: 214, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28606583
10.
Distal axonopathy in an alsin-deficient mouse model.
Hum Mol Genet
; 16(23): 2911-20, 2007 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17855450
11.
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria.
Proc Natl Acad Sci U S A
; 103(18): 7142-7, 2006 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-16636275