Tutkijat / Oulu  | Ala-Kokko, L. |
 | Ala-Kokko, T(ero) |
 | Ala-Korpela, M(ika) |
 | Alahuhta, S. |
 | Alén, M(arkku) |
 | Antikainen, R. |
 | Anttonen, V(uokko) |
 | Biancari, F(austo) |
 | Bloigu, R(isto) |
 | Eskelinen, S. |
 | Flinkkilä, T(apio) |
 | Hakkola, J. |
 | Hallman, M. |
 | Hartikainen, A(nna)-L(iisa) |
 | Hausen, H. |
 | Hautala, N(ina) |
 | Hautala, T(imo) |
 | Heape, A. |
 | Herzig, K(arl)-H(einz) |
 | Hillbom, M. |
 | Hiltunen, J.K. |
 | Hörkko, S. |
 | Huikuri, H(eikki) |
 | Hukkanen J(anne) |
 | Ignatius, J. |
 | Isohanni, M. |
 | Jaakkola, J. |
 | Jaakkola, M(aritta) S. |
 | Jaakola, V-P. |
 | Jämsä, T(imo) |
 | Janhonen, S. |
 | Jartti, T(uomas) |
 | Järvelin, M(arjo)-R(iitta) |
 | Jokelainen, J(ari) |
 | Juffer, A(ndré) H. |
 | Junttila, J(uhani) |
 | Juvonen, T. |
 | Kaarteenaho, R(iitta) |
 | Kajantie, E(ero)*(THL/OY) |
 | Karppinen (Koivunen), P(eppi) |
 | Karppinen, J(aro) |
 | Karttunen, T.J. |
 | Keinänen-Kiukaanniemi, S(irkka) |
 | Kerkelä, R(isto) |
 | Kesäniemi, Y(rjö) A(ntero) |
 | Kettunen, J(ohannes) |
 | Kietzmann, T(homas). |
 | Kivirikko, K.I. |
 | Knuuttila, M. |
 | Koivukangas, J. |
 | Kursula, P(etri) |
 | Kyngäs, H. |
 | Larivaara, P. |
 | Larmas, M. |
 | Lehenkari, P(etri) |
 | Lehtiö, L(ari) |
 | Leppilahti, J. |
 | Luukinen, H. |
 | Mainio A |
 | Majamaa, K. |
 | Mäki, P(irjo) |
 | Mäkikallio, T(imo) H. |
 | Männikkö, M(inna) |
 | Manninen, A(ki). |
 | Martikainen, H(annu) |
 | Miettunen, J(ouko) |
 | Myllyharju, J(ohanna) |
 | Myllylä, R. |
 | Myllylä, V. |
 | Näyhä, S(imo) |
 | Neubauer, P. |
 | Nieminen, M(iika) T. |
 | Nieminen, P(entti) |
 | Niinimäki, J(aakko) |
 | Ohukainen, P(auli) |
 | Oikarinen, A. |
 | Oikarinen, K. |
 | Pelkonen, O(lavi) |
 | Petäjä-Repo, U.E. |
 | Pihlajaniemi, T(aina) |
 | Pirttiniemi, P(ertti) |
 | Puistola, U(lla) |
 | Rajaniemi, H.J. |
 | Räsänen, P. |
 | Raustia, A. |
 | Remes, A(nne) |
 | Risteli, J. |
 | Ristiniemi, J. |
 | Ruddock, L.W. |
 | Ruokonen, A. |
 | Ryynänen, M. |
 | Saarakkala, S. |
 | Saari, A. |
 | Salo, T(uula) |
 | Sándor, G(eorge) K. |
 | Savolainen, E-R. |
 | Savolainen, M.J. |
 | Savolainen, O. |
 | Sillanpää, M(ikko). |
 | Soininen, R. |
 | Sorri, M. |
 | Taanila, A. |
 | Tapiainen, T(erhi) |
 | Tervonen, O(smo) |
 | Timonen, M(arkku) |
 | Turpeenniemi-Hujanen, T. |
 | Tuukkanen, J(uha) |
 | Tuulonen, A. |
 | Uhari, M. |
 | Ukkola, O(lavi) |
 | Uusimaa, J. |
 | Vainio, O. |
 | Vainio, S. |
 | Väyrynen, J(uha) P. |
 | Veijola, J(uha) |
 | Veijola, R(iitta) |
 | Virokannas, H. |
 | Voipio, H(anna)-M(arja) |
 | Vuolteenaho, O. |
 | Weckström, M. |
 | Wei, GH. |
 | Wierenga, R.K. |
 | Winqvist, R(obert) |
 | Ylänne, J. |
 | Ylitalo, K(ari) | Scholar Chart >>
|
»My Articles
»Latest Feeds
»Popular Feeds |
| | Association of mitochondrial DNA haplogroups J and K with low response in exercise training among Finnish military conscripts | Majamaa, K. | 22 hours | save |  |  |  |  |
| Carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is a risk factor for ALS in the Finnish population | Majamaa, K. | 22 hours | save |  |  |  |  |
| Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis | Majamaa, K. | 22 hours | save |  |  |  |  |
| Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia | Majamaa, K. | 22 hours | save |  |  |  |  |
| Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies | Majamaa, K. | 22 hours | save |  |  |  |  |
| Analysis of functional variants in mitochondrial DNA of Finnish athletes | Majamaa, K. | 22 hours | save |  |  |  |  |
| Mitochondrial DNA variation in sudden cardiac death: a population-based study | Majamaa, K. | 22 hours | save |  |  |  |  |
| HTT haplogroups in Finnish patients with Huntington disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| Prehospital and hospital delays for stroke patients treated with thrombolysis: A retrospective study from mixed rural-urban area in Northern Finland | Majamaa, K. | 22 hours | save |  |  |  |  |
| Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, andα-synuclein mechanisms | Majamaa, K. | 22 hours | save |  |  |  |  |
| Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy | Majamaa, K. | 22 hours | save |  |  |  |  |
| Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype | Majamaa, K. | 22 hours | save |  |  |  |  |
| The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype | Majamaa, K. | 22 hours | save |  |  |  |  |
| Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family | Majamaa, K. | 22 hours | save |  |  |  |  |
| Genetic risk factors in Finnish patients with Parkinson's disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairment | Majamaa, K. | 22 hours | save |  |  |  |  |
| Comparison of mid-age-onset and late-onset Huntington's disease in Finnish patients | Majamaa, K. | 22 hours | save |  |  |  |  |
| Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study | Majamaa, K. | 22 hours | save |  |  |  |  |
| Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder | Majamaa, K. | 22 hours | save |  |  |  |  |
| Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study | Majamaa, K. | 22 hours | save |  |  |  |  |
| A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| Psychiatric and neurological disorders are associated with bullous pemphigoid - a nationwide Finnish Care Register study | Majamaa, K. | 22 hours | save |  |  |  |  |
| A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism | Majamaa, K. | 22 hours | save |  |  |  |  |
| Chronic subdural hematomas in Finnish patients with Huntington's disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| Comorbid epilepsy in Finnish patients with adult-onset Huntington's disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms | Majamaa, K. | 22 hours | save |  |  |  |  |
| Glycosaminoglycans in subdural fluid and CSF after meningeal injury | Majamaa, K. | 22 hours | save |  |  |  |  |
| Epidemiology of stroke in Finnish patients with Huntington's disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| A 13-year follow-up of Finnish patients with Salla disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA | Majamaa, K. | 22 hours | save |  |  |  |  |
| Epidemiology of early-onset Parkinson's disease in Finland | Majamaa, K. | 22 hours | save |  |  |  |  |
| Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes | Majamaa, K. | 22 hours | save |  |  |  |  |
| Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based study | Majamaa, K. | 22 hours | save |  |  |  |  |
| Effects of pathogenic mutations in membrane subunits of mitochondrial Complex I on redox activity and proton translocation studied by modeling in Escherichia coli | Majamaa, K. | 22 hours | save |  |  |  |  |
| Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment | Majamaa, K. | 22 hours | save |  |  |  |  |
| Epidemiology of Huntington's disease in Finland | Majamaa, K. | 22 hours | save |  |  |  |  |
| Investments of research and treatment of brain diseases will pay of time | Majamaa, K. | 22 hours | save |  |  |  |  |
| Childhood hearing impairment in northern Finland, etiology and additional disabilities | Majamaa, K. | 22 hours | save |  |  |  |  |
| Response to Dobie | Majamaa, K. | 22 hours | save |  |  |  |  |
| Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantation | Majamaa, K. | 22 hours | save |  |  |  |  |
| WFS1 mutations in hearing-impaired children | Majamaa, K. | 22 hours | save |  |  |  |  |
| Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunction | Majamaa, K. | 22 hours | save |  |  |  |  |
| The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific | Majamaa, K. | 22 hours | save |  |  |  |  |
| Variations of mitochondrial DNA polymeraseγ in patients with Parkinson's disease | Majamaa, K. | 22 hours | save |  |  |  |  |
| Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk | Majamaa, K. | 22 hours | save |  |  |  |  |
| Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus | Majamaa, K. | 22 hours | save |  |  |  |  |
| Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patient | Majamaa, K. | 22 hours | save |  |  |  |  |
| New treatments for mitochondrial disease-no time to drop our standards | Majamaa, K. | 22 hours | save |  |  |  |  |
| Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a report of three adult patients | Majamaa, K. | 22 hours | save |  |  |  |  |
| Characterization of chronic subdural hematoma fluid proteome | Majamaa, K. | 22 hours | save |  |  |  |  |
|  report | next » | |
|