Results 101 to 110 of about 15,044 (185)

Mixed Brain Pathologies in Dementia: The BrainNet Europe Consortium Experience [PDF]

, 2008
Background: Dementia results from heterogeneous diseases of the brain. Mixed disease forms are increasingly recognized. Methods: We performed a survey within brain banks of BrainNet Europe to estimate the proportion of mixed disease forms underlying ...
Al-Sarraj, Safa, Alafuzoff, Irina, Arzberger, Thomas, Bogdanovic, Nenad, Budka, Herbert, Capellari, Sabina, Ferrer, Isidro, Gelpi, Ellen, Kovacs, Gabor G., Kovari, Viktor, Kretzschmar, Hans, Nagy, Zoltan, Parchi, Piero, Seilhean, Danielle, Soininen, Hilkka, Troakes, Claire   +15 more
core   +1 more source

The Paper-Toss Test: enhancing bedside recognition of corticobasal syndrome

Frontiers in Neurology
IntroductionThe diagnosis of corticobasal syndrome (CBS) is challenging due to its clinical overlap with other neurodegenerative disorders. Ideomotor apraxia is a core feature of CBS and often presents asymmetrically, but is often under-recognized in the
Gero Lueg, Thomas Duning, Markus A. Hobert, Markus A. Hobert, Alexander Rösler, Sara Peranovic, Rainer Wirth, Julia Krämer   +7 more
doaj   +1 more source

Heritability in frontotemporal tauopathies

Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, 2019
Introduction Exploring the degree of heritability in a large cohort of frontotemporal lobar degeneration with tau‐immunopositive inclusions (FTLD‐tau) and determining if different FTLD‐tau subtypes are associated with stronger heritability will provide ...
Shelley L. Forrest, Glenda M. Halliday, Heather McCann, Andrew B. McGeachie, Ciara V. McGinley, John R. Hodges, Olivier Piguet, John B. Kwok, Maria G. Spillantini, Jillian J. Kril   +9 more
doaj   +1 more source

Alien hand and leg as the presenting feature of probable sporadic Creutzfeldt-Jakob disease: A rare presentation of a rare disease

Annals of Indian Academy of Neurology, 2015
Sporadic Creutzfeldt-Jakob disease (sCJD) can have varied clinical presentation depending upon the genotype at codon 129. The common presenting clinical features of sCJD are rapid onset cognitive impairment, ataxia, psychosis and visual signs (field ...
Banshi Lal Kumawat, Chandra Mohan Sharma, Kunal Nath, Mihir Acharya, Dinesh Khandelwal, Deepak Jain   +5 more
doaj   +1 more source

Cryo-EM structures of tau filaments from SH-SY5Y cells seeded with brain extracts from cases of Alzheimer's disease and corticobasal degeneration. [PDF]

FEBS Open Bio, 2023
Tarutani A, Lövestam S, Zhang X, Kotecha A, Robinson AC, Mann DMA, Saito Y, Murayama S, Tomita T, Goedert M, Scheres SHW, Hasegawa M.   +11 more
europepmc   +2 more sources

Neurofilament Light Chain in Cerebrospinal Fluid and Blood in Multiple System Atrophy: A Systematic Review and Meta-Analysis

Brain Sciences
Background/Objectives: Multiple system atrophy (MSA) presents a challenging diagnosis due to its clinical overlap with other neurodegenerative disorders, especially other α-synucleinopathies.
Silvia Demiri, Dimitra Veltsista, Vasileios Siokas, Kanellos C. Spiliopoulos, Antonia Tsika, Polyxeni Stamati, Elisabeth Chroni, Efthimios Dardiotis, Ioannis Liampas   +8 more
doaj   +1 more source

Gestural buffer impairment in early onset Corticobasal Degeneration: a single-case study [PDF]

Neuropsychological Trends, 2008
We investigated limb apraxia in a case of a clinically diagnosed Corticobasal Degeneration with early onset (48 years) in a right handed woman. We used a new battery for the assessment of limb apraxia, based on a cognitive model of praxis. This cognitive
Michele Poletti, Barbara Nucciarone, Filippo Baldacci, Angelo Nuti, Claudio Lucetti, Paolo Del Dotto, Caterina Berti, Chiara Logi, Ubaldo Bonuccelli   +8 more
doaj  

Clinical course of pathologically confirmed corticobasal degeneration and corticobasal syndrome. [PDF]

Brain Commun, 2023
Aiba I, Hayashi Y, Shimohata T, Yoshida M, Saito Y, Wakabayashi K, Komori T, Hasegawa M, Ikeuchi T, Tokumaru AM, Sakurai K, Murayama S, Hasegawa K, Uchihara T, Toyoshima Y, Saito Y, Yabe I, Tanikawa S, Sugaya K, Hayashi K, Sano T, Takao M, Sakai M, Fujimura H, Takigawa H, Adachi T, Hanajima R, Yokota O, Miki T, Iwasaki Y, Kobayashi M, Arai N, Ohkubo T, Yokota T, Mori K, Ito M, Ishida C, Tanaka M, Idezuka J, Kanazawa M, Aoki K, Aoki M, Hasegawa T, Watanabe H, Hashizume A, Niwa H, Yasui K, Ito K, Washimi Y, Mukai E, Kubota A, Toda T, Nakashima K, J-VAC study group .   +53 more
europepmc   +1 more source

Clinical course in corticobasal syndrome and corticobasal degeneration: implications for diagnosis and management. [PDF]

Brain Commun, 2023
McGeachan RI, King D.
europepmc   +1 more source

Rapidly Progressive Corticobasal Degeneration Mimicking Brainstem Encephalitis. [PDF]

Mov Disord Clin Pract, 2023
Moura J, Oliveira V, Sardoeira A, Pinto M, Gelpi E, Taipa R, Santos E.   +6 more
europepmc   +1 more source