Remes AM - Search Results

1

Corrigendum to "Risk factors for reactivation of clinical disease activity in multiple sclerosis after natalizumab cessation" [Multiple Sclerosis and Related Disorders 38 (2020) 101498].

Mustonen T, Rauma I, Hartikainen P, Krüger J, Niiranen M, Selander T, Simula S, Remes AM, Kuusisto H. Mustonen T, et al. Among authors: remes am. Mult Scler Relat Disord. 2020 Jun;41:102107. doi: 10.1016/j.msard.2020.102107. Epub 2020 Apr 18. Mult Scler Relat Disord. 2020. PMID: 32571611 No abstract available.

2

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: remes am. 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

3

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. Among authors: remes am. BMC Neurol. 2008 Dec 17;8:48. doi: 10.1186/1471-2377-8-48. BMC Neurol. 2008. PMID: 19091059 Free PMC article.

4

Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degeneration.

Krüger J, Hinttala R, Majamaa K, Remes AM. Krüger J, et al. Among authors: remes am. Mol Neurodegener. 2010 Feb 2;5:8. doi: 10.1186/1750-1326-5-8. Mol Neurodegener. 2010. PMID: 20181062 Free PMC article.

5

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. Among authors: remes am. Eur J Neurol. 2010 Nov;17(11):1393-5. doi: 10.1111/j.1468-1331.2010.03028.x. Eur J Neurol. 2010. PMID: 20412296

6

Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.

Krüger J, Moilanen V, Majamaa K, Remes AM. Krüger J, et al. Among authors: remes am. Alzheimer Dis Assoc Disord. 2012 Jul-Sep;26(3):272-6. doi: 10.1097/WAD.0b013e318231e6c7. Alzheimer Dis Assoc Disord. 2012. PMID: 21959359

7

Cortical thickness in frontotemporal dementia, mild cognitive impairment, and Alzheimer's disease.

Hartikainen P, Räsänen J, Julkunen V, Niskanen E, Hallikainen M, Kivipelto M, Vanninen R, Remes AM, Soininen H. Hartikainen P, et al. Among authors: remes am. J Alzheimers Dis. 2012;30(4):857-74. doi: 10.3233/JAD-2012-112060. J Alzheimers Dis. 2012. PMID: 22466003

8

C9ORF72 expansion does not affect the phenotype in Nasu-Hakola disease with the DAP12 mutation.

Solje E, Hartikainen P, Valori M, Vanninen R, Tiihonen J, Hakola P, Tienari PJ, Remes AM. Solje E, et al. Among authors: remes am. Neurobiol Aging. 2014 Jul;35(7):1780.e13-7. doi: 10.1016/j.neurobiolaging.2014.01.149. Epub 2014 Feb 5. Neurobiol Aging. 2014. PMID: 24612676

9

Cerebrospinal fluid biomarkers for Alzheimer's disease in patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis with the C9ORF72 repeat expansion.

Kämäläinen A, Herukka SK, Hartikainen P, Helisalmi S, Moilanen V, Knuuttila A, Jansson L, Tienari PJ, Remes AM. Kämäläinen A, et al. Among authors: remes am. Dement Geriatr Cogn Disord. 2015;39(5-6):287-93. doi: 10.1159/000371704. Epub 2015 Mar 13. Dement Geriatr Cogn Disord. 2015. PMID: 25791939

10

Neurological comorbidity and survival in multiple sclerosis.

Krökki O, Bloigu R, Ansakorpi H, Reunanen M, Remes AM. Krökki O, et al. Among authors: remes am. Mult Scler Relat Disord. 2014 Jan;3(1):72-7. doi: 10.1016/j.msard.2013.06.006. Epub 2013 Jul 18. Mult Scler Relat Disord. 2014. PMID: 25877976

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