Detalhe da pesquisa
1.
Generation of a human induced pluripotent stem cell line (UQi001-A-1) edited with the CRISPR-Cas9 system to carry the heterozygous TARDBP c.1144G > A (p.A382T) missense mutation.
Stem Cell Res
; 70: 103137, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37315423
2.
ALSUntangled #65: glucocorticoid corticosteroids.
Amyotroph Lateral Scler Frontotemporal Degener
; 24(3-4): 351-357, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35997522
3.
Altered TDP-43 Structure and Function: Key Insights into Aberrant RNA, Mitochondrial, and Cellular and Systemic Metabolism in Amyotrophic Lateral Sclerosis.
Metabolites
; 12(8)2022 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36005581
4.
Evaluation of an Australian neurological nurse-led model of postdischarge care.
Health Soc Care Community
; 30(4): e962-e973, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34245179
5.
Winners and Losers in Palliative Care Service Delivery: Time for a Public Health Approach to Palliative and End of Life Care.
Healthcare (Basel)
; 9(12)2021 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34946341
6.
Why and how the work of Motor Neurone Disease Associations matters before and during bereavement: a consumer perspective.
Palliat Care Soc Pract
; 15: 26323524211009537, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34104885
7.
Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease.
Amyotroph Lateral Scler Frontotemporal Degener
; 22(1-2): 12-22, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32909457
8.
Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study.
Amyotroph Lateral Scler Frontotemporal Degener
; 21(7-8): 593-605, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32668960
9.
Structural Variants May Be a Source of Missing Heritability in sALS.
Front Neurosci
; 14: 47, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32082115
10.
Association of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis.
Neurol Genet
; 6(2): e406, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32185242