Tuominen H - Search Results

1

Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy.

Remes AM, Finnilä S, Mononen H, Tuominen H, Takalo R, Herva R, Majamaa K. Remes AM, et al. Among authors: tuominen h. Neurology. 2004 Jul 27;63(2):234-40. doi: 10.1212/01.wnl.0000129988.68657.fa. Neurology. 2004. PMID: 15277614

2

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: tuominen h. BMC Neurol. 2008 Dec 17;8:48. doi: 10.1186/1471-2377-8-48. BMC Neurol. 2008. PMID: 19091059 Free PMC article.

3

Carbon 11-labeled pittsburgh compound B positron emission tomographic amyloid imaging in patients with APP locus duplication.

Remes AM, Laru L, Tuominen H, Aalto S, Kemppainen N, Mononen H, Någren K, Parkkola R, Rinne JO. Remes AM, et al. Among authors: tuominen h. Arch Neurol. 2008 Apr;65(4):540-4. doi: 10.1001/archneur.65.4.540. Arch Neurol. 2008. PMID: 18413480

4

POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.

Komulainen T, Hinttala R, Kärppä M, Pajunen L, Finnilä S, Tuominen H, Rantala H, Hassinen I, Majamaa K, Uusimaa J. Komulainen T, et al. Among authors: tuominen h. BMC Neurol. 2010 May 3;10:29. doi: 10.1186/1471-2377-10-29. BMC Neurol. 2010. PMID: 20438629 Free PMC article.

5

Amyloid myopathy: a diagnostic challenge.

Tuomaala H, Kärppä M, Tuominen H, Remes AM. Tuomaala H, et al. Among authors: tuominen h. Neurol Int. 2009 Nov 16;1(1):e7. doi: 10.4081/ni.2009.e7. Neurol Int. 2009. PMID: 21577365 Free PMC article.

6

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage.

Rovelet-Lecrux A, Frebourg T, Tuominen H, Majamaa K, Campion D, Remes AM. Rovelet-Lecrux A, et al. Among authors: tuominen h. J Neurol Neurosurg Psychiatry. 2007 Oct;78(10):1158-9. doi: 10.1136/jnnp.2006.113514. Epub 2007 Apr 18. J Neurol Neurosurg Psychiatry. 2007. PMID: 17442758 Free PMC article. No abstract available.

7

Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder.

Kytövuori L, Kärppä M, Tuominen H, Uusimaa J, Saari M, Hinttala R, Majamaa K. Kytövuori L, et al. Among authors: tuominen h. BMC Neurol. 2017 May 18;17(1):96. doi: 10.1186/s12883-017-0883-5. BMC Neurol. 2017. PMID: 28521807 Free PMC article.

8

Cytoskeletal structure in cells harboring two mutations: R133C in NOTCH3 and 5650G>A in mitochondrial DNA.

Annunen-Rasila J, Kärppä M, Finnilä S, Ylä-Outinen H, Veijola J, Tuominen H, Peltonen J, Majamaa K. Annunen-Rasila J, et al. Among authors: tuominen h. Mitochondrion. 2007 Feb-Apr;7(1-2):96-100. doi: 10.1016/j.mito.2006.11.004. Epub 2006 Dec 5. Mitochondrion. 2007. PMID: 17276737

9

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. Among authors: tuominen h. 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.

10

Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes.

Komulainen T, Hautakangas MR, Hinttala R, Pakanen S, Vähäsarja V, Lehenkari P, Olsen P, Vieira P, Saarenpää-Heikkilä O, Palmio J, Tuominen H, Kinnunen P, Majamaa K, Rantala H, Uusimaa J. Komulainen T, et al. Among authors: tuominen h. JIMD Rep. 2015;23:91-100. doi: 10.1007/8904_2015_438. Epub 2015 May 5. JIMD Rep. 2015. PMID: 25940035 Free PMC article.

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