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Old age genetically confirmed frontotemporal lobar degeneration with TDP‐43 has limbic predominant TDP‐43 deposition
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Primary Age‐Related Tauopathy (PART) in a Finnish Population‐Based Study of the Oldest Old (Vantaa 85+)
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Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathy
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Brain TDP‐43 pathology in corticobasal degeneration: topographical correlation with neuronal loss
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Long‐standing multiple system atrophy‐Parkinsonism with limbic and FTLD‐type α‐synuclein pathology
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Correlations in post‐mortem imaging‐histopathology studies of sporadic human cerebral small vessel disease: A systematic review
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Distinct brain‐derived TDP‐43 strains from FTLD‐TDP subtypes induce diverse morphological TDP‐43 aggregates and spreading patterns in vitro and in vivo
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TDP‐43 proteinopathy occurs independently of autophagic substrate accumulation and underlies nuclear defects in Niemann‐Pick C disease
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Machine learning‐based decision tree classifier for the diagnosis of progressive supranuclear palsy and corticobasal degeneration
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Atypical astroglial pTDP‐43 pathology in astroglial predominant tauopathy
We observed atypical astrocytic pTDP-43 pathology in astroglial predominant tauopathy.
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Spatial molecular profiling of a central nervous system low‐grade diffusely infiltrative tumour with INI1 deficiency featuring a high‐grade atypical teratoid/rhabdoid tumour component
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Longstanding Multiple System Atrophy‐Parkinsonism with Limbic and FTLD‐type α‐Synuclein Pathology
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Concurrent tau pathologies in frontotemporal lobar degeneration with TDP‐43 pathology
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Alpha adaptins show isoform‐specific association with neurofibrillary tangles in Alzheimer’s disease.
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Non‐coding regulatory elements: potential roles in disease and the case of epilepsy
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Spatial molecular profiling of a central nervous system low‐grade diffusely infiltrative tumour with INI1 deficiency (CNS LGDIT‐INI1) featuring a high‐grade AT/RT component
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