Hietala M - Search Results

1

Epidemiology of Huntington's disease in Finland.

Sipilä JO, Hietala M, Siitonen A, Päivärinta M, Majamaa K. Sipilä JO, et al. Among authors: hietala m. Parkinsonism Relat Disord. 2015 Jan;21(1):46-9. doi: 10.1016/j.parkreldis.2014.10.025. Epub 2014 Nov 3. Parkinsonism Relat Disord. 2015. PMID: 25466405 Free article.

2

Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion.

Juvonen V, Hietala M, Päivärinta M, Rantamäki M, Hakamies L, Kaakkola S, Vierimaa O, Penttinen M, Savontaus ML. Juvonen V, et al. Among authors: hietala m. Ann Neurol. 2000 Sep;48(3):354-61. Ann Neurol. 2000. PMID: 10976642

3

Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutation.

Martikainen MH, Päivärinta M, Hietala M, Kaasinen V. Martikainen MH, et al. Among authors: hietala m. Neurol Genet. 2015 Oct 15;1(4):e27. doi: 10.1212/NXG.0000000000000027. eCollection 2015 Dec. Neurol Genet. 2015. PMID: 27066564 Free PMC article.

4

SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population.

Pasanen P, Palin E, Pohjolan-Pirhonen R, Pöyhönen M, Rinne JO, Päivärinta M, Martikainen MH, Kaasinen V, Hietala M, Gardberg M, Saukkonen AM, Eerola-Rautio J, Kaakkola S, Lyytinen J, Tienari PJ, Paetau A, Suomalainen A, Myllykangas L. Pasanen P, et al. Among authors: hietala m. Neurobiol Aging. 2017 Feb;50:168.e5-168.e8. doi: 10.1016/j.neurobiolaging.2016.10.014. Epub 2016 Oct 19. Neurobiol Aging. 2017. PMID: 27838048

5

HTT haplogroups in Finnish patients with Huntington disease.

Ylönen S, Sipilä JOT, Hietala M, Majamaa K. Ylönen S, et al. Among authors: hietala m. Neurol Genet. 2019 Apr 22;5(3):e334. doi: 10.1212/NXG.0000000000000334. eCollection 2019 Jun. Neurol Genet. 2019. PMID: 31086827 Free PMC article.

6

Wilson's Disease in Finland: A Nationwide Population-Based Study.

Sipilä JOT, Hietala M, Kytö V, Kaasinen V. Sipilä JOT, et al. Among authors: hietala m. Mov Disord. 2020 Dec;35(12):2323-2327. doi: 10.1002/mds.28207. Epub 2020 Jul 2. Mov Disord. 2020. PMID: 32618023 Free article.

7

Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland.

Hietala M, Hakonen A, Aro AR, Niemelä P, Peltonen L, Aula P. Hietala M, et al. Am J Hum Genet. 1995 Jun;56(6):1493-500. Am J Hum Genet. 1995. PMID: 7762573 Free PMC article.

8

Prospects of carrier screening of aspartylglucosaminuria in Finland.

Hietala M, Grön K, Syvänen AC, Peltonen L, Aula P. Hietala M, et al. Eur J Hum Genet. 1993;1(4):296-300. doi: 10.1159/000472427. Eur J Hum Genet. 1993. PMID: 8081942

9

The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.

Juvonen V, Hietala M, Kairisto V, Savontaus ML. Juvonen V, et al. Among authors: hietala m. Acta Neurol Scand. 2005 Mar;111(3):154-62. doi: 10.1111/j.1600-0404.2005.00349.x. Acta Neurol Scand. 2005. PMID: 15691283

10

No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome.

Vahteristo P, Koski TA, Näätsaari L, Kiuru M, Karhu A, Herva R, Sallinen SL, Vierimaa O, Björck E, Richard S, Gardie B, Bessis D, Van Glabeke E, Blanco I, Houlston R, Senter L, Hietala M, Aittomäki K, Aaltonen LA, Launonen V, Lehtonen R. Vahteristo P, et al. Among authors: hietala m. Fam Cancer. 2010 Jun;9(2):245-51. doi: 10.1007/s10689-009-9312-2. Fam Cancer. 2010. PMID: 20091131

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