Difficulties in the diagnosis of four repeats (4R) tauopathic parkinsonian syndromes

P Alster, E Krzyżanowska… - neurologia i …, 2018 - journals.viamedica.pl
Abstract Corticobasal Degeneration Degeneration (CBD) and Progressive Supranuclear
Palsy (PSP) are types of four repeats (4R) tauopathies, which are associated to …

Frontotemporal lobar degeneration–tau as a pied piper?

M Tolnay, A Probst - Neurogenetics, 2002 - Springer
Frontotemporal lobar degeneration (FTLD) is the second most-common form of cortical
dementia in the presenium after Alzheimer disease. Clinically three disease entities can be …

Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases

K Tsuchiya, S Murayama, K Mitani, T Oda, K Arima… - Acta …, 2005 - Springer
This report concerns a clinicopathological study of three additional patients with corticobasal
degeneration (CBD), described here for the first time, and a clinicopathological correlation …

Distribution of tuft-shaped astrocytes in the cerebral cortex in progressive supranuclear palsy

Y Iwasaki, M Yoshida, M Hattori, A Goto, I Aiba… - Acta …, 2004 - Springer
The deposition of abnormal levels of tau protein is a major neuropathological feature of
progressive supranuclear palsy (PSP), and the presence of tuft-shaped astrocytes is a …

Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal …

CF Tan, YS Piao, A Kakita, M Yamada, H Takano… - Acta …, 2005 - Springer
We report two patients who exhibited frontotemporal dementia (FTD) with unusual
neuropathological features. The ages of the patients at death were 65 and 67 years, the …

[HTML][HTML] Tauopathy in basal ganglia involvement is exacerbated in a subset of patients with Alzheimer's disease: The Hisayama study

H Hamasaki, H Honda, SO Suzuki, M Shijo… - Alzheimer's & Dementia …, 2019 - Elsevier
Introduction We have conducted the pathological cohort study of autopsied cases of
Hisayama residents to reveal a recent trend of dementia-related pathology. We noticed a …

Genetic forms of tauopathies: inherited causes and implications of Alzheimer's disease-like TAU pathology in primary and secondary tauopathies

F Langerscheidt, T Wied, MA Al Kabbani… - Journal of …, 2024 - Springer
Tauopathies are a heterogeneous group of neurologic diseases characterized by
pathological axodendritic distribution, ectopic expression, and/or phosphorylation and …

Macroscopic diagnostic clue for parkinsonism

M Yoshida, A Akagi, H Miyahara, Y Riku… - …, 2022 - Wiley Online Library
The neuropathological background of parkinsonism includes various neurodegenerative
disorders, including Lewy body disease (LBD), multiple system atrophy (MSA), progressive …

Pathology of oligodendroglia: An overview

T Komori - Neuropathology, 2017 - Wiley Online Library
Oligodendroglia are cells responsible for creating myelin sheaths for axons in the CNS.
However, pathologies of oligodendroglia other than demyelination are not well understood …

Diffuse neurofibrillary tangles with calcification (Kosaka–Shibayama disease) in Japan

K Ukai, K Kosaka - Psychiatry and Clinical Neurosciences, 2016 - Wiley Online Library
Diffuse neurofibrillary tangles with calcification (DNTC) is a rare, pre‐senile type of
dementia. The term 'DNTC'was initially proposed by Kosaka in 1994. Although 26 autopsies …