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The Blood‐CSF‐Brain Route of Neurological Disease: The Indirect Pathway into the Brain.
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Irisin treatment lowers levels of phosphorylated tau in the hippocampus of pre‐symptomatic female but not male htau mice
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Old age genetically confirmed frontotemporal lobar degeneration with TDP‐43 has limbic predominant TDP‐43 deposition
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Loss of the metabolism and sleep regulating neuronal populations expressing orexin and oxytocin in the hypothalamus in amyotrophic lateral sclerosis
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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
Key Points We investigated the presence of intranuclear inclusions in skin biopsies from patients with oculopharyngodistal...
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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
Abstract Aim The heterogeneity in the distribution and morphological features of TAR DNA-binding protein-43 (TDP-43) patho...
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TDP‐43 proteinopathy occurs independently of autophagic substrate accumulation and underlies nuclear defects in Niemann‐Pick C disease
Abstract Aims Neuronal cytoplasmic inclusions of TAR-DNA binding protein of 43 kDa (TDP-43) are a pathological hallma...
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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
Abstract Multiple system atrophy (MSA) is a sporadic neurodegenerative disease clinically marked by autonomic failure and ...
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Automated immunofluorescence analysis for sensitive and precise dystrophin quantification in muscle biopsies
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The desmin mutation R349P increases contractility and fragility of stem cell‐generated muscle micro‐tissues
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AKT1E17K‐mutated meningioma cell lines respond to treatment with the AKT inhibitor AZD5363
Abstract Objectives Meningiomas are the most frequent primary brain tumours. Recently, knowledge about the molecular drive...
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Dysfunction of the blood‐brain barrier in Alzheimer’s disease: evidence from human studies
Abstract The pathological processes leading to synapse loss, neuronal loss, brain atrophy and gliosis in Alzheimer´s ...
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Concurrent tau pathologies in frontotemporal lobar degeneration with TDP‐43 pathology
Abstract Aims Accumulating evidence suggests that patients with frontotemporal lobar degeneration (FTLD) can have patholog...
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Neuropathology of a patient with Alzheimer disease treated with low doses of Verubecestat
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Combinatorial model of amyloid β and tau reveals synergy between amyloid deposits and tangle formation
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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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Neurotherapeutic implications of sense and respond strategies generated by astrocytes and astrocytic tumours to combat pH mechanical stress
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Interfering with lysophosphatidic acid receptor edg2/lpa1 signalling slows down disease progression in SOD1‐G93A transgenic mice
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Implementation of TERT promoter mutations improve prognostication of the WHO classification in meningioma
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