Results 1 to 10 of about 12,036 (197)

Apraxia and motor dysfunction in corticobasal syndrome. [PDF]

open access: yesPLoS ONE, 2014
BACKGROUND: Corticobasal syndrome (CBS) is characterized by multifaceted motor system dysfunction and cognitive disturbance; distinctive clinical features include limb apraxia and visuospatial dysfunction. Transcranial magnetic stimulation (TMS) has been
James R Burrell   +4 more
doaj   +10 more sources

Neuronal antibody-associated corticobasal syndrome [PDF]

open access: yesAnnals of Indian Academy of Neurology, 2023
Anu Gupta   +10 more
doaj   +4 more sources

The Discourse Profile in Corticobasal Syndrome: A Comprehensive Clinical and Biomarker Approach [PDF]

open access: yesBrain Sciences, 2022
The aim of this study was to characterize the oral discourse of CBS patients and to verify whether measures obtained during a semi-spontaneous speech production could differentiate CBS patients from controls.
Isabel Junqueira de Almeida   +8 more
doaj   +2 more sources

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

open access: yesFrontiers 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   +7 more
doaj   +2 more sources

Corticobasal syndrome mimicking Foix-Chavany-Marie syndrome with suggested 4-repeat tauopathy by tau PET [PDF]

open access: yesBMC Geriatrics, 2023
Background Corticobasal syndrome (CBS) is a neurodegenerative disease diagnosed based on clinical manifestations such as asymmetrical parkinsonism, limb apraxia, and speech and language impairment. The background pathology of CBS is commonly a variety of
Kosei Nakamura   +9 more
doaj   +2 more sources

Phenotypic and Positron Emission Tomography with [18F]fluordeoxyglucose (FDG PET) differences in corticobasal syndrome: comparison of two cases [PDF]

open access: yesDementia & Neuropsychologia
Corticobasal syndrome (CBS) is a rare cause of dementia and comprises varied combinations of subcortical signs (akinetic-rigid parkinsonism, dystonia, or myoclonus) with cortical signs (apraxia, alien hand or cortical sensory deficit), usually asymmetric.
Thais Winkeler Beltrão   +8 more
doaj   +2 more sources

Unilateral tactile agnosia as an onset symptom of corticobasal syndrome [PDF]

open access: yesFrontiers in Human Neuroscience
Tactile agnosia is the inability to recognize objects via haptic exploration, in the absence of an elementary sensory deficit. Traditionally, it has been described as a disturbance in extracting information about the physical properties of objects ...
Laura Facci   +14 more
doaj   +2 more sources

A progranulin gene deletion in frontotemporal lobar degeneration with corticobasal syndrome in a TREDEM case report [PDF]

open access: yesJournal of Alzheimer's Disease Reports
Background Behavioral variant frontotemporal dementia usually presents with behavioral and personality changes, social disinhibition, apathy, and lack of empathy, and is characterized by atrophy of the frontal and temporal lobes. Corticobasal syndrome is
Maurizio Gallucci   +7 more
doaj   +2 more sources

Language in corticobasal syndrome: a systematic review

open access: yesDementia & Neuropsychologia, 2021
. Language is commonly impacted in corticobasal syndrome (CBS). However, the profile and type of language assessment in CBS are poorly studied. Objective: To identify language impairments in CBS.
Isabel Junqueira de Almeida   +4 more
doaj   +1 more source

The Significance of Asymmetry in the Assessment of Brain Perfusion in Atypical Tauopathic Parkinsonian Syndromes

open access: yesDiagnostics, 2022
Progressive supranuclear palsy syndrome (PSPS) and corticobasal syndrome (CBS) are clinical manifestations of tauopathic Parkinsonian syndromes. Due to their overlapping symptomatology, the differential diagnosis of these entities may be difficult when ...
Piotr Alster   +6 more
doaj   +1 more source

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