Alien Limb Phenomenon and Ideomotor Apraxia as Early Indicators of Sporadic Creutzfeldt-Jakob Disease. [PDF]
Movement Disorders Clinical Practice, Volume 12, Issue 8, Page 1187-1189, August 2025.
Lueg G, Kleffner I, Hobert MA.
europepmc +2 more sources
Neural basis of motor symptoms in Alzheimer's disease: role of regional tau burden and cognition. [PDF]
Abstract INTRODUCTION With accumulating evidence that motor manifestations in Alzheimer's disease (AD) may emerge from AD pathology independent of other copathologies, we investigated the neural basis of motor dysfunction under the amyloid/tau/neurodegeneration (ATN) framework.
Na HK +8 more
europepmc +2 more sources
A Rare Case Report of Neuroimaging, Electrophysiological, and Dynamic Laryngoscopy Studies in a Stroke Patient of Foix-Chavany-Marie Syndrome. [PDF]
ABSTRACT Foix‐Chavany‐Marie Syndrome (FCMS), also known as opercular syndrome, is a rare neurological disorder caused by an ischemic stroke that results in autonomic‐voluntary dissociation. In this case report, we describe a patient who presented with an acute right frontal and parietal cortical lesion, in addition to a remote infarction in the left ...
Xia L +7 more
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Clinicopathological and Neuroimaging Correlates of Disease Duration in Primary Progressive Apraxia of Speech. [PDF]
ABSTRACT Background Primary progressive apraxia of speech is a neurodegenerative disorder characterized by early, isolated speech impairment due to impairment of motor speech planning and programming. Patients with PPAOS have varying disease durations from the estimated onset of the first symptom to death.
Hossain N +9 more
europepmc +2 more sources
Clinical detection of corticobasal syndrome, beyond an “atypical" Alzheimer's [PDF]
Abstract Corticobasal syndrome (CBS) corresponds to a progressive deterioration of motor and associative cognitive functions that include ideomotor apraxia, astereognosis/loss of graphesthesia, sensory extinction, alien limb in combination with marked asymmetric limb dystonia, rigidity or myoclonus.
Flores I +3 more
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Managing Dystonia in Partington Syndrome. [PDF]
Abstract Background Bilateral focal hand dystonia is an almost pathognomonic sign of Partington syndrome, frequently accompanied by intellectual disability and oromotor dyspraxia. However, a few studies have focused on the treatment of this focal dystonia, making patient management uncertain.
Pichon E +13 more
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Apraxias in neurodegenerative dementias
Background: Apraxia is a state of inability to carry out a learned motor act in the absence of motor, sensory or cerebellar defect on command processed through the Praxis circuit.
Sadanandavalli Retnaswami Chandra +2 more
doaj +1 more source
An autopsy-proven case of Corticobasal degeneration heralded by Pontine infarction
Background Neurodegenerative disorders are characterized by insidious progression with poorly-delineated long latent period. Antecedent clinical insult could rarely unmask latent neurodegenerative disorders.
Dallah Yoo +3 more
doaj +1 more source
Selective contralesional constructional hemi-apraxia after unilateral brain damage: Which relationship with unilateral spatial neglect? [PDF]
Abstract We describe a peculiar contralesional drawing disorder in three patients affected by focal brain lesions, who did not show signs of unilateral neglect at standard clinical assessment, including the star cancellation test. This picture, that could be termed selective constructional hemi‐apraxia (CHA), could follow both right and left‐hemisphere
Panico F, Arini A, Crisci C, Trojano L.
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Longitudinal Videofluorographic Dysphagia Measures in Progressive Supranuclear Palsy. [PDF]
Abstract Background Dysphagia can lead to fatal aspiration pneumonia in progressive supranuclear palsy (PSP). Little is known about the longitudinal progression of dysphagia or whether it differs across PSP clinical variants. Objectives To characterize longitudinal changes in dysphagia across PSP variants and determine relationships with disease ...
Cattani AC +8 more
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