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2. Distribution of Lewy-related pathology in the brain, spinal cord, and periphery: the population-based Vantaa 85 + study

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4. Frequency of LATE neuropathologic change across the spectrum of Alzheimer’s disease neuropathology: combined data from 13 community-based or population-based autopsy cohorts

5. Primary age‐related tauopathy in a Finnish population‐based study of the oldest old (Vantaa 85+)

6. Forecasting stroke-like episodes and outcomes in mitochondrial disease

7. Alpha-synuclein pathology of olfactory bulbs/peduncles in the Vantaa85+ cohort exhibit two divergent patterns: a population-based study

10. Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans

11. Neuropathological consensus criteria for the evaluation of Lewy pathology in post-mortem brains: a multi-centre study

12. TDP-43 proteinopathies: a new wave of neurodegenerative diseases

13. Loss of capillary pericytes and the blood–brain barrier in white matter in poststroke and vascular dementias and Alzheimer’s disease

16. Small vessel disease pathological changes in neurodegenerative and vascular dementias concomitant with autonomic dysfunction

18. Prediction models for dementia and neuropathology in the oldest old: the Vantaa 85+ cohort study

19. Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease

20. Melatonin receptor type 1A gene linked to Alzheimer’s disease in old age

23. Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)

24. MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypes

25. Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains

28. Frontal white matter hyperintensities, clasmatodendrosis and gliovascular abnormalities in ageing and post-stroke dementia

30. Genome‐wide association study of neocortical Lewy‐related pathology

31. Phenotypic variability of TRPV4 related neuropathies

32. EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia

36. Expanding The Clinical And Genetic Spectrum Of MYH7 Related Skeletal Myopathies In The United Kingdom (P3.302)

37. Two recurrent mutations are associated with GNE myopathy in the North of Britain

39. Plasma homocysteine, Alzheimer and cerebrovascular pathology: a population-based autopsy study

41. Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNAGlu(MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

44. Delirium is a strong risk factor for dementia in the oldest-old: a population-based cohort study

47. APOE and AβPP Gene Variation in Cortical and Cerebrovascular Amyloid-β Pathology and Alzheimer's Disease: A Population-Based Analysis