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AddAla-Kokko, L.
AddAla-Kokko, T(ero)
AddAla-Korpela, M(ika)
AddAlahuhta, S.
AddAlén, M(arkku)
AddAntikainen, R.
AddAnttonen, V(uokko)
AddBiancari, F(austo)
AddBloigu, R(isto)
AddEskelinen, S.
AddFlinkkilä, T(apio)
AddHakkola, J.
AddHallman, M.
AddHartikainen, A(nna)-L(iisa)
AddHausen, H.
AddHautala, N(ina)
AddHautala, T(imo)
AddHeape, A.
AddHerzig, K(arl)-H(einz)
AddHillbom, M.
AddHiltunen, J.K.
AddHörkko, S.
AddHuikuri, H(eikki)
AddHukkanen J(anne)
AddIgnatius, J.
AddIsohanni, M.
AddJaakkola, J.
AddJaakkola, M(aritta) S.
AddJaakola, V-P.
AddJämsä, T(imo)
AddJanhonen, S.
AddJartti, T(uomas)
AddJärvelin, M(arjo)-R(iitta)
AddJokelainen, J(ari)
AddJuffer, A(ndré) H.
AddJunttila, J(uhani)
AddJuvonen, T.
AddKaarteenaho, R(iitta)
AddKajantie, E(ero)*(THL/OY)
AddKarppinen (Koivunen), P(eppi)
AddKarppinen, J(aro)
AddKarttunen, T.J.
AddKeinänen-Kiukaanniemi, S(irkka)
AddKerkelä, R(isto)
AddKesäniemi, Y(rjö) A(ntero)
AddKettunen, J(ohannes)
AddKietzmann, T(homas).
AddKivirikko, K.I.
AddKnuuttila, M.
AddKoivukangas, J.
AddKursula, P(etri)
AddKyngäs, H.
AddLarivaara, P.
AddLarmas, M.
AddLehenkari, P(etri)
AddLehtiö, L(ari)
AddLeppilahti, J.
AddLuukinen, H.
AddMainio A
AddMajamaa, K.
AddMäki, P(irjo)
AddMäkikallio, T(imo) H.
AddMännikkö, M(inna)
AddManninen, A(ki).
AddMartikainen, H(annu)
AddMiettunen, J(ouko)
AddMyllyharju, J(ohanna)
AddMyllylä, R.
AddMyllylä, V.
AddNäyhä, S(imo)
AddNeubauer, P.
AddNieminen, M(iika) T.
AddNieminen, P(entti)
AddNiinimäki, J(aakko)
AddOhukainen, P(auli)
AddOikarinen, A.
AddOikarinen, K.
AddPelkonen, O(lavi)
AddPetäjä-Repo, U.E.
AddPihlajaniemi, T(aina)
AddPirttiniemi, P(ertti)
AddPuistola, U(lla)
AddRajaniemi, H.J.
AddRäsänen, P.
AddRaustia, A.
AddRemes, A(nne)
AddRisteli, J.
AddRistiniemi, J.
AddRuddock, L.W.
AddRuokonen, A.
AddRyynänen, M.
AddSaarakkala, S.
AddSaari, A.
AddSalo, T(uula)
AddSándor, G(eorge) K.
AddSavolainen, E-R.
AddSavolainen, M.J.
AddSavolainen, O.
AddSillanpää, M(ikko).
AddSoininen, R.
AddSorri, M.
AddTaanila, A.
AddTapiainen, T(erhi)
AddTervonen, O(smo)
AddTimonen, M(arkku)
AddTurpeenniemi-Hujanen, T.
AddTuukkanen, J(uha)
AddTuulonen, A.
AddUhari, M.
AddUkkola, O(lavi)
AddUusimaa, J.
AddVainio, O.
AddVainio, S.
AddVäyrynen, J(uha) P.
AddVeijola, J(uha)
AddVeijola, R(iitta)
AddVirokannas, H.
AddVoipio, H(anna)-M(arja)
AddVuolteenaho, O.
AddWeckström, M.
AddWei, GH.
AddWierenga, R.K.
AddWinqvist, R(obert)
AddYlänne, J.
AddYlitalo, K(ari)

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Association of mitochondrial DNA haplogroups J and K with low response in exercise training among Finnish military conscriptsMajamaa, K.22 hourssaveRefWorksSFX Info
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Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysisMajamaa, K.22 hourssaveRefWorksSFX Info
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementiaMajamaa, K.22 hourssaveRefWorksSFX Info
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studiesMajamaa, K.22 hourssaveRefWorksSFX Info
Analysis of functional variants in mitochondrial DNA of Finnish athletesMajamaa, K.22 hourssaveRefWorksSFX Info
Mitochondrial DNA variation in sudden cardiac death: a population-based studyMajamaa, K.22 hourssaveRefWorksSFX Info
HTT haplogroups in Finnish patients with Huntington diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
Prehospital and hospital delays for stroke patients treated with thrombolysis: A retrospective study from mixed rural-urban area in Northern FinlandMajamaa, K.22 hourssaveRefWorksSFX Info
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, andα-synuclein mechanismsMajamaa, K.22 hourssaveRefWorksSFX Info
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 epilepsyMajamaa, K.22 hourssaveRefWorksSFX Info
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotypeMajamaa, K.22 hourssaveRefWorksSFX Info
The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotypeMajamaa, K.22 hourssaveRefWorksSFX Info
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational familyMajamaa, K.22 hourssaveRefWorksSFX Info
Genetic risk factors in Finnish patients with Parkinson's diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairmentMajamaa, K.22 hourssaveRefWorksSFX Info
Comparison of mid-age-onset and late-onset Huntington's disease in Finnish patientsMajamaa, K.22 hourssaveRefWorksSFX Info
Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based StudyMajamaa, K.22 hourssaveRefWorksSFX Info
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorderMajamaa, K.22 hourssaveRefWorksSFX Info
Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association studyMajamaa, K.22 hourssaveRefWorksSFX Info
A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
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A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadismMajamaa, K.22 hourssaveRefWorksSFX Info
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Comorbid epilepsy in Finnish patients with adult-onset Huntington's diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
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Glycosaminoglycans in subdural fluid and CSF after meningeal injuryMajamaa, K.22 hourssaveRefWorksSFX Info
Epidemiology of stroke in Finnish patients with Huntington's diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
A 13-year follow-up of Finnish patients with Salla diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNAMajamaa, K.22 hourssaveRefWorksSFX Info
Epidemiology of early-onset Parkinson's disease in FinlandMajamaa, K.22 hourssaveRefWorksSFX Info
Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel PhenotypesMajamaa, K.22 hourssaveRefWorksSFX Info
Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based studyMajamaa, K.22 hourssaveRefWorksSFX Info
Effects of pathogenic mutations in membrane subunits of mitochondrial Complex I on redox activity and proton translocation studied by modeling in Escherichia coliMajamaa, K.22 hourssaveRefWorksSFX Info
Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairmentMajamaa, K.22 hourssaveRefWorksSFX Info
Epidemiology of Huntington's disease in FinlandMajamaa, K.22 hourssaveRefWorksSFX Info
Investments of research and treatment of brain diseases will pay of timeMajamaa, K.22 hourssaveRefWorksSFX Info
Childhood hearing impairment in northern Finland, etiology and additional disabilitiesMajamaa, K.22 hourssaveRefWorksSFX Info
Response to DobieMajamaa, K.22 hourssaveRefWorksSFX Info
Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantationMajamaa, K.22 hourssaveRefWorksSFX Info
WFS1 mutations in hearing-impaired childrenMajamaa, K.22 hourssaveRefWorksSFX Info
Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunctionMajamaa, K.22 hourssaveRefWorksSFX Info
The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specificMajamaa, K.22 hourssaveRefWorksSFX Info
Variations of mitochondrial DNA polymeraseγ in patients with Parkinson's diseaseMajamaa, K.22 hourssaveRefWorksSFX Info
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic riskMajamaa, K.22 hourssaveRefWorksSFX Info
Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitusMajamaa, K.22 hourssaveRefWorksSFX Info
Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patientMajamaa, K.22 hourssaveRefWorksSFX Info
New treatments for mitochondrial disease-no time to drop our standardsMajamaa, K.22 hourssaveRefWorksSFX Info
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 patientsMajamaa, K.22 hourssaveRefWorksSFX Info
Characterization of chronic subdural hematoma fluid proteomeMajamaa, K.22 hourssaveRefWorksSFX Info
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