Works matching AU Majamaa K
Results: 16
Complex segregation analysis of Parkinson's disease in the Finnish population.
- Published in:
- Human Genetics, 2001, v. 108, n. 3, p. 184, doi. 10.1007/s004390100470
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- Publication type:
- Article
Mutations in EIF4G1 are not a common cause of Parkinson's disease.
- Published in:
- European Journal of Neurology, 2013, v. 20, n. 4, p. e59, doi. 10.1111/ene.12051
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- Publication type:
- Article
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients.
- Published in:
- European Journal of Neurology, 2010, v. 17, n. 11, p. 1393, doi. 10.1111/j.1468-1331.2010.03028.x
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- Publication type:
- Article
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration.
- Published in:
- European Journal of Neurology, 2009, v. 16, n. 1, p. 27, doi. 10.1111/j.1468-1331.2008.02272.x
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- Publication type:
- Article
Molecular genetic analysis of the α-synuclein and the parkin gene in Parkinson's disease in Finland.
- Published in:
- European Journal of Neurology, 2002, v. 9, n. 5, p. 479, doi. 10.1046/j.1468-1331.2002.00458.x
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- Publication type:
- Article
Rapid Induction of Meningeal Collagen Synthesis in the Cerebral Cisternal and Ventricular Compartments after Subarachnoid Hemorrhage.
- Published in:
- Acta Neurochirurgica, 2001, v. 143, n. 8, p. 821, doi. 10.1007/s007010170036
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- Publication type:
- Article
Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 2, p. 64
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- Publication type:
- Article
m.3243A>G mutation in mitochondrial DNA leads to decreased insulin sensitivity in skeletal muscle and to progressive beta-cell dysfunction.
- Published in:
- 2009
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- Publication type:
- journal article
Epidemiology of stroke in Finnish patients with Huntington's disease.
- Published in:
- Acta Neurologica Scandinavica, 2016, v. 134, n. 1, p. 61, doi. 10.1111/ane.12512
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- Publication type:
- Article
Secondary metabolic effects in complex I deficiency.
- Published in:
- 2005
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- Publication type:
- Journal Article
Adult-onset ataxia and polyneuropathy caused by mitochondrial 8993T-->C mutation.
- Published in:
- 2005
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- Publication type:
- Journal Article
An Analysis of Finnish Debtors Who Defaulted in 2014–2016 Because of Unsecured Credit Products.
- Published in:
- Journal of Consumer Policy, 2022, v. 45, n. 4, p. 595, doi. 10.1007/s10603-022-09525-4
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- Publication type:
- Article
Debt Judgments as a Reflection of Consumption-Related Debt Problems.
- Published in:
- Journal of Consumer Policy, 2019, v. 42, n. 2, p. 223, doi. 10.1007/s10603-018-9402-3
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- Publication type:
- Article
Variations of mitochondrial DNA polymerase γ in patients with Parkinson’s disease.
- Published in:
- Journal of Neurology, 2013, v. 260, n. 12, p. 3144, doi. 10.1007/s00415-013-7132-7
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- Publication type:
- Article
Improved adherence to practice guidelines yields better outcome in high-risk patients with acute coronary syndrome without ST elevation: findings from nationwide FINACS studies.
- Published in:
- Journal of Internal Medicine, 2004, v. 256, n. 4, p. 316, doi. 10.1111/j.1365-2796.2004.01374.x
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- Publication type:
- Article
Spectrum of myopathic findings in 50 patients with the 3243A<G mutation in mitochondrial DNA.
- Published in:
- 2005
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- Publication type:
- Journal Article