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LRRK2 mutations are not common in Alzheimer's disease.
Toft M, Sando SB, Melquist S, Ross OA, White LR, Aasly JO, Farrer MJ. Toft M, et al. Among authors: aasly jo. Mech Ageing Dev. 2005 Nov;126(11):1201-5. doi: 10.1016/j.mad.2005.06.010. Mech Ageing Dev. 2005. PMID: 16087219
PINK1 mutation heterozygosity and the risk of Parkinson's disease.
Toft M, Myhre R, Pielsticker L, White LR, Aasly JO, Farrer MJ. Toft M, et al. Among authors: aasly jo. J Neurol Neurosurg Psychiatry. 2007 Jan;78(1):82-4. doi: 10.1136/jnnp.2006.097840. J Neurol Neurosurg Psychiatry. 2007. PMID: 17172567 Free PMC article.
LRRK2 and Parkinson's disease in Norway.
Toft M, Haugarvoll K, Ross OA, Farrer MJ, Aasly JO. Toft M, et al. Among authors: aasly jo. Acta Neurol Scand Suppl. 2007;187:72-5. doi: 10.1111/j.1600-0404.2007.00852.x. Acta Neurol Scand Suppl. 2007. PMID: 17419834
Metabolomic profiling in LRRK2-related Parkinson's disease.
Johansen KK, Wang L, Aasly JO, White LR, Matson WR, Henchcliffe C, Beal MF, Bogdanov M. Johansen KK, et al. PLoS One. 2009 Oct 22;4(10):e7551. doi: 10.1371/journal.pone.0007551. PLoS One. 2009. PMID: 19847307 Free PMC article.
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease.
Aasly JO, Vilariño-Güell C, Dachsel JC, Webber PJ, West AB, Haugarvoll K, Johansen KK, Toft M, Nutt JG, Payami H, Kachergus JM, Lincoln SJ, Felic A, Wider C, Soto-Ortolaza AI, Cobb SA, White LR, Ross OA, Farrer MJ. Aasly JO, et al. Mov Disord. 2010 Oct 15;25(13):2156-63. doi: 10.1002/mds.23265. Mov Disord. 2010. PMID: 20669305 Free PMC article.
268 results