Remes AM - Search Results

1

NDUFA1 p.Gly32Arg variant in early-onset dementia.

Huttula S, Väyrynen H, Helisalmi S, Kytövuori L, Luukkainen L, Hiltunen M, Remes AM, Krüger J. Huttula S, et al. Among authors: remes am. Neurobiol Aging. 2022 Jun;114:113-116. doi: 10.1016/j.neurobiolaging.2021.09.026. Epub 2022 Jan 21. Neurobiol Aging. 2022. PMID: 35131137 Free article.

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

Cerebrospinal fluid antibodies to oxidized LDL are increased in Alzheimer's disease.

Kankaanpää J, Turunen SP, Moilanen V, Hörkkö S, Remes AM. Kankaanpää J, et al. Among authors: remes am. Neurobiol Dis. 2009 Mar;33(3):467-72. doi: 10.1016/j.nbd.2008.12.001. Epub 2008 Dec 16. Neurobiol Dis. 2009. PMID: 19130885

5

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.

6

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

7

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

8

Genetic loci associated with Alzheimer's disease and cerebrospinal fluid biomarkers in a Finnish case-control cohort.

Elias-Sonnenschein LS, Helisalmi S, Natunen T, Hall A, Paajanen T, Herukka SK, Laitinen M, Remes AM, Koivisto AM, Mattila KM, Lehtimäki T, Verhey FR, Visser PJ, Soininen H, Hiltunen M. Elias-Sonnenschein LS, et al. Among authors: remes am. PLoS One. 2013;8(4):e59676. doi: 10.1371/journal.pone.0059676. Epub 2013 Apr 3. PLoS One. 2013. PMID: 23573206 Free PMC article.

9

WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims.

Kytövuori L, Seppänen A, Martikainen MH, Moilanen JS, Kamppari S, Särkioja T, Remes AM, Räsänen P, Rönnemaa T, Majamaa K. Kytövuori L, et al. Among authors: remes am. J Hum Genet. 2013 Aug;58(8):495-500. doi: 10.1038/jhg.2013.29. Epub 2013 Apr 18. J Hum Genet. 2013. PMID: 23595122

10

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

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