Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
8 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Neuron. 2011 Oct 20;72(2):257-68. doi: 10.1016/j.neuron.2011.09.010. Epub 2011 Sep 21.
Neuron. 2011.
PMID: 21944779
Free PMC article.
Novel TARDBP sequence variant and C9ORF72 repeat expansion in a family with frontotemporal dementia.
Kaivorinne AL, Moilanen V, Kervinen M, Renton AE, Traynor BJ, Majamaa K, Remes AM.
Kaivorinne AL, et al.
Alzheimer Dis Assoc Disord. 2014 Apr-Jun;28(2):190-3. doi: 10.1097/WAD.0b013e318266fae5.
Alzheimer Dis Assoc Disord. 2014.
PMID: 22892647
Free PMC article.
Item in Clipboard
Clinical Characteristics of C9ORF72-Linked Frontotemporal Lobar Degeneration.
Kaivorinne AL, Bode MK, Paavola L, Tuominen H, Kallio M, Renton AE, Traynor BJ, Moilanen V, Remes AM.
Kaivorinne AL, et al.
Dement Geriatr Cogn Dis Extra. 2013 Aug 20;3(1):251-62. doi: 10.1159/000351859. eCollection 2013.
Dement Geriatr Cogn Dis Extra. 2013.
PMID: 24052799
Free PMC article.
Item in Clipboard
Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland.
Kaivorinne AL, Krüger J, Kuivaniemi K, Tuominen H, Moilanen V, Majamaa K, Remes AM.
Kaivorinne AL, et al.
BMC Neurol. 2008 Dec 17;8:48. doi: 10.1186/1471-2377-8-48.
BMC Neurol. 2008.
PMID: 19091059
Free PMC article.
Item in Clipboard
Fulminant neuromyelitis optica in a Finnish woman - a case report.
Kaivorinne AL, Lintunen J, Baumann P.
Kaivorinne AL, et al.
Clin Case Rep. 2016 Jul 11;4(8):782-5. doi: 10.1002/ccr3.624. eCollection 2016 Aug.
Clin Case Rep. 2016.
PMID: 27525084
Free PMC article.
Item in Clipboard
Slowly progressive frontotemporal lobar degeneration caused by the C9ORF72 repeat expansion: a 20-year follow-up study.
Suhonen NM, Kaivorinne AL, Moilanen V, Bode M, Takalo R, Hänninen T, Remes AM.
Suhonen NM, et al. Among authors: kaivorinne al.
Neurocase. 2015 Feb;21(1):85-9. doi: 10.1080/13554794.2013.873057. Epub 2014 Jan 14.
Neurocase. 2015.
PMID: 24417314
Item in Clipboard
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients.
Kaivorinne AL, Krüger J, Udd B, Majamaa K, Remes AM.
Kaivorinne AL, et al.
Eur J Neurol. 2010 Nov;17(11):1393-5. doi: 10.1111/j.1468-1331.2010.03028.x.
Eur J Neurol. 2010.
PMID: 20412296
Item in Clipboard
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration.
Krüger J, Kaivorinne AL, Udd B, Majamaa K, Remes AM.
Krüger J, et al. Among authors: kaivorinne al.
Eur J Neurol. 2009 Jan;16(1):27-30. doi: 10.1111/j.1468-1331.2008.02272.x. Epub 2008 Nov 25.
Eur J Neurol. 2009.
PMID: 19049508
Item in Clipboard
Cite
Cite