Mathias Toft
Mathias Toft
Department of Neurology, Oslo University Hospital
Verifisert e-postadresse på medisin.uio.no
TittelSitert avÅr
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
J Kachergus, IF Mata, M Hulihan, JP Taylor, S Lincoln, J Aasly, JM Gibson, ...
The American Journal of Human Genetics 76 (4), 672-680, 2005
5222005
Lrrk2 and Lewy body disease
OA Ross, M Toft, AJ Whittle, JL Johnson, S Papapetropoulos, DC Mash, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
2532006
Clinical features of LRRK2‐associated Parkinson's disease in central Norway
JO Aasly, M Toft, I Fernandez‐Mata, J Kachergus, M Hulihan, LR White, ...
Annals of Neurology: Official Journal of the American Neurological …, 2005
1792005
Linkage disequilibrium and association of MAPT H1 in Parkinson disease
L Skipper, K Wilkes, M Toft, M Baker, S Lincoln, M Hulihan, OA Ross, ...
The American Journal of Human Genetics 75 (4), 669-677, 2004
1442004
Novel pathogenic LRRK2 p. Asn1437His substitution in familial Parkinson's disease
JO Aasly, C Vilariño‐Güell, JC Dachsel, PJ Webber, AB West, ...
Movement disorders 25 (13), 2156-2163, 2010
1032010
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
CM Lill, A Rengmark, L Pihlstrøm, I Fogh, A Shatunov, PM Sleiman, ...
Alzheimer's & Dementia 11 (12), 1407-1416, 2015
1002015
Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population
M Toft, L Pielsticker, OA Ross, JO Aasly, MJ Farrer
Neurology 66 (3), 415-417, 2006
982006
Multiple alpha‐synuclein gene polymorphisms are associated with Parkinson’s disease in a Norwegian population
R Myhre, M Toft, J Kachergus, MM Hulihan, JO Aasly, H Klungland, ...
Acta Neurologica Scandinavica 118 (5), 320-327, 2008
862008
Surgical site infections after deep brain stimulation surgery: frequency, characteristics and management in a 10-year period
S Bjerknes, IM Skogseid, T Sæhle, E Dietrichs, M Toft
PloS one 9 (8), e105288, 2014
792014
Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease
L Pihlstrøm, G Axelsson, KA Bjørnarå, N Dizdar, C Fardell, L Forsgren, ...
Neurobiology of aging 34 (6), 1708. e7-1708. e13, 2013
782013
MAPK‐pathway activity, Lrrk2 G2019S, and Parkinson's disease
LR White, M Toft, SN Kvam, MJ Farrer, JO Aasly
Journal of neuroscience research 85 (6), 1288-1294, 2007
742007
Parkinson's disease: the genetics of a heterogeneous disorder
D Gosal, OA Ross, M Toft
European journal of neurology 13 (6), 616-627, 2006
642006
Genomewide association, Parkinson disease, and PARK10
MJ Farrer, K Haugarvoll, OA Ross, JT Stone, NM Milkovic, SA Cobb, ...
The American Journal of Human Genetics 78 (6), 1084-1088, 2006
622006
Parkinsonism, FXTAS, and FMR1 premutations
M Toft, J Aasly, G Bisceglio, CH Adler, RJ Uitti, A Krygowska‐Wajs, ...
Movement disorders: official journal of the Movement Disorder Society 20 (2 …, 2005
592005
FMR1 Premutations Associated With Fragile X–Associated Tremor/Ataxia Syndrome in Multiple System Atrophy
V Biancalana, M Toft, I Le Ber, F Tison, E Scherrer, S Thibodeau, ...
Archives of neurology 62 (6), 962-966, 2005
562005
Parkinson's disease correlates with promoter methylation in the α‐synuclein gene
L Pihlstrøm, V Berge, A Rengmark, M Toft
Movement Disorders 30 (4), 577-580, 2015
542015
REM sleep behavior disorder in Parkinson's disease–Is there a gender difference?
KA Bjørnarå, E Dietrichs, M Toft
Parkinsonism & related disorders 19 (1), 120-122, 2013
492013
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions
JC Dächsel, OA Ross, IF Mata, J Kachergus, M Toft, A Cannon, M Baker, ...
Acta neuropathologica 113 (5), 601-606, 2007
492007
PINK1 mutation heterozygosity and the risk of Parkinson’s disease
M Toft, R Myhre, L Pielsticker, LR White, JO Aasly, MJ Farrer
Journal of Neurology, Neurosurgery & Psychiatry 78 (1), 82-84, 2007
482007
LRRK2 mutations and Parkinsonism
M Toft, IF Mata, JM Kachergus, OA Ross, MJ Farrer
The Lancet 365 (9466), 1229-1230, 2005
452005
Systemet kan ikke utføre handlingen. Prøv igjen senere.
Artikler 1–20