Open Save New
FeedNavigator / National Library of Health Sciences
Tutkijat / Oulu
AddAla-Kokko, L.
AddAla-Kokko, T(ero)
AddAla-Korpela, M(ika)
AddAlahuhta, S.
AddAlen, M.
AddAntikainen, R.
AddAnttonen, V(uokko)
AddBiancari, F.
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
AddHukkanen J(anne)
AddIgnatius, J.
AddIsohanni, M.
AddJaakkola, J.
AddJaakkola, M(aritta) S.
AddJaakola, V-P.
AddJämsä, T(imo)
AddJanhonen, S.
AddJärvelin, M(arjo)-R(iitta)
AddJokelainen, J(ari)
AddJuffer, A.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.A.
AddKettunen, J(ohannes)
AddKietzmann, T(homas).
AddKivirikko, K.I.
AddKnuuttila, M.
AddKoivukangas, J.
AddKursula, P.
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.
AddMännikkö, M(inna)
AddManninen, A(ki).
AddMartikainen, H(annu)
AddMiettunen, J(ouko)
AddMyllyharju, J.
AddMyllylä, R.
AddMyllylä, V.
AddNäyhä, S.
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.
AddPirttiniemi, P(ertti)
AddPuistola, U(lla)
AddRajaniemi, H.J.
AddRämet, M(ika)
AddRäsänen, P.
AddRaustia, A.
AddRemes, A(nne)
AddRisteli, J.
AddRistiniemi, J.
AddRuddock, L.W.
AddRuokonen, A.
AddRuskoaho, H.
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)
AddTjäderhane, L.
AddTurpeenniemi-Hujanen, T.
AddTuukkanen, J(uha)
AddTuulonen, A.
AddUhari, M.
AddUkkola, O(lavi)
AddUusimaa, J.
AddVainio, O.
AddVainio, S.
AddVeijola, J(uha)
AddVeijola, R(iitta)
AddVirokannas, H.
AddVoipio, H(anna)-M(arja)
AddVuolteenaho, O.
AddWeckström, M.
AddWei, GH.
AddWierenga, R.K.
AddWinqvist, R.
AddYlänne, J.
AddYlitalo, K(ari)

Scholar Chart >>

»My Articles

»Latest Feeds

»Popular Feeds
Search Feed Catalog by Name:

Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.Majamaa, K.238 dayssaveRefWorks
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.Majamaa, K.258 dayssaveRefWorks
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.Majamaa, K.271 dayssaveRefWorks
Analysis of functional variants in mitochondrial DNA of Finnish athletes.Majamaa, K.281 dayssaveRefWorks
Mitochondrial DNA variation in sudden cardiac death: a population-based study.Majamaa, K.430 dayssaveRefWorks
HTT haplogroups in Finnish patients with Huntington disease.Majamaa, K.449 dayssaveRefWorks
Prehospital and hospital delays for stroke patients treated with thrombolysis: A retrospective study from mixed rural-urban area in Northern Finland.Majamaa, K.461 dayssaveRefWorks
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, andα-synuclein mechanisms.Majamaa, K.486 dayssaveRefWorks
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.680 dayssaveRefWorks
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.Majamaa, K.686 dayssaveRefWorks
The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.Majamaa, K.946 dayssaveRefWorks
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family.Majamaa, K.983 dayssaveRefWorks
Genetic risk factors in Finnish patients with Parkinson's disease.Majamaa, K.1025 dayssaveRefWorks
A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairment.Majamaa, K.1038 dayssaveRefWorks
Comparison of mid-age-onset and late-onset Huntington's disease in Finnish patients.Majamaa, K.1074 dayssaveRefWorks
Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study.Majamaa, K.1086 dayssaveRefWorks
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder.Majamaa, K.1175 dayssaveRefWorks
Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study.Majamaa, K.1252 dayssaveRefWorks
A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease.Majamaa, K.1272 dayssaveRefWorks
Epidemiology of stroke in Finnish patients with Huntington's disease.Majamaa, K.1343 dayssaveRefWorks
Psychiatric and neurological disorders are associated with bullous pemphigoid - a nationwide Finnish Care Register study.Majamaa, K.1360 dayssaveRefWorks
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.1458 dayssaveRefWorks
Chronic subdural hematomas in Finnish patients with Huntington's disease.Majamaa, K.1520 dayssaveRefWorks
Comorbid epilepsy in Finnish patients with adult-onset Huntington's disease.Majamaa, K.1639 dayssaveRefWorks
Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms.Majamaa, K.1765 dayssaveRefWorks
Glycosaminoglycans in subdural fluid and CSF after meningeal injury.Majamaa, K.1772 dayssaveRefWorks
Epidemiology of stroke in Finnish patients with Huntington's disease.Majamaa, K.1777 dayssaveRefWorks
A 13-year follow-up of Finnish patients with Salla disease.Majamaa, K.1836 dayssaveRefWorks
Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.Majamaa, K.1836 dayssaveRefWorks
Epidemiology of early-onset Parkinson's disease in Finland.Majamaa, K.1881 dayssaveRefWorks
Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes.Majamaa, K.1921 dayssaveRefWorks
Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based study.Majamaa, K.1926 dayssaveRefWorks
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.1977 dayssaveRefWorks
Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment.Majamaa, K.2011 dayssaveRefWorks
Epidemiology of Huntington's disease in Finland.Majamaa, K.2074 dayssaveRefWorks
[Investments of research and treatment of brain diseases will pay of time].Majamaa, K.2136 dayssaveRefWorks
Childhood hearing impairment in northern Finland, etiology and additional disabilities.Majamaa, K.2162 dayssaveRefWorks
Response to Dobie.Majamaa, K.2184 dayssaveRefWorks
Acute liver failure after valproate exposure in patients with POLG1 mutations and its prognosis after liver transplantation.Majamaa, K.2200 dayssaveRefWorks
WFS1 mutations in hearing-impaired children.Majamaa, K.2251 dayssaveRefWorks
Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunction.Majamaa, K.2363 dayssaveRefWorks
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.2424 dayssaveRefWorks
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.Majamaa, K.2456 dayssaveRefWorks
Variations of mitochondrial DNA polymeraseγ in patients with Parkinson's disease.Majamaa, K.2489 dayssaveRefWorks
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.2557 dayssaveRefWorks
Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.Majamaa, K.2573 dayssaveRefWorks
Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patient.Majamaa, K.2585 dayssaveRefWorks
New treatments for mitochondrial disease-no time to drop our standards.Majamaa, K.2592 dayssaveRefWorks
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.2648 dayssaveRefWorks
Characterization of Chronic Subdural Hematoma Fluid Proteome.Majamaa, K.2655 dayssaveRefWorks
 XML / RSS feed
next »