Detalhe da pesquisa
1.
Cultured lymphocytes' mitochondrial genome integrity is not altered by cladribine.
Clin Exp Immunol
; 214(3): 304-313, 2023 12 13.
Artigo
Inglês
| MEDLINE | ID: mdl-37860849
2.
A novel class of somatic mutations in blood detected preferentially in CD8+ cells.
Clin Immunol
; 175: 75-81, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27932211
3.
Cerebrospinal fluid biomarkers for Alzheimer's disease in patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis with the C9ORF72 repeat expansion.
Dement Geriatr Cogn Disord
; 39(5-6): 287-93, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25791939
4.
Brain ¹8F-FDG and ¹¹C-PiB PET findings in two siblings with FTD/ALS associated with the C9ORF72 repeat expansion.
Neurocase
; 20(2): 150-7, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-23216213
5.
Epstein-Barr Virus in the Cerebrospinal Fluid and Blood Compartments of Patients With Multiple Sclerosis and Controls.
Neurol Neuroimmunol Neuroinflamm
; 11(3): e200226, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38608226
6.
C9orf72 hexanucleotide repeat allele tagging SNPs: Associations with ALS risk and longevity.
Front Genet
; 14: 1087098, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36936421
7.
High prevalence of low-allele-fraction somatic mutations in STAT3 in peripheral blood CD8+ cells in multiple sclerosis patients and controls.
PLoS One
; 17(11): e0278245, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36441748
8.
ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the C9orf72 Hexanucleotide Repeat Expansion.
Neurol Genet
; 8(2): e665, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-35295181
9.
CD8+ cell somatic mutations in multiple sclerosis patients and controls-Enrichment of mutations in STAT3 and other genes implicated in hematological malignancies.
PLoS One
; 16(12): e0261002, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34874980
10.
Carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is a risk factor for ALS in the Finnish population.
Acta Neuropathol Commun
; 8(1): 187, 2020 11 09.
Artigo
Inglês
| MEDLINE | ID: mdl-33168078
11.
C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition.
Neurobiol Aging
; 84: 242.e7-242.e12, 2019 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30979436
12.
Heterozygous TYROBP deletion (PLOSLFIN) is not a strong risk factor for cognitive impairment.
Neurobiol Aging
; 64: 159.e1-159.e4, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29336840
13.
Cerebrospinal Fluid TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis Patients with and without the C9ORF72 Hexanucleotide Expansion.
Dement Geriatr Cogn Dis Extra
; 6(1): 142-9, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27195002
14.
Amyloid precursor protein (APP) A673T mutation in the elderly Finnish population.
Neurobiol Aging
; 34(5): 1518.e1-3, 2013 May.
Artigo
Inglês
| MEDLINE | ID: mdl-23102935
15.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Neuron
; 72(2): 257-68, 2011 Oct 20.
Artigo
Inglês
| MEDLINE | ID: mdl-21944779
16.
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
Lancet Neurol
; 9(10): 978-85, 2010 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20801718