Results 301 to 310 of about 900,695 (398)

Structural Alterations in the Gray Matter Volume in Rapid‐Onset Dystonia‐Parkinsonism

open access: yesMovement Disorders, EarlyView.
Abstract Background Previously, we identified decreased thalamic blood flow in patients with ATP1A3 variants. Objective This study evaluated structural gray matter organization in rapid‐onset dystonia‐parkinsonism (RDP) patients compared with controls and two phenotypically overlapping movement disorders.
Ihtsham U. Haq   +7 more
wiley   +1 more source

Electrophysiological Evidence for Impaired Central Pain Modulation in Parkinson's Disease

open access: yesMovement Disorders, EarlyView.
Our study demonstrates electrophysiological evidence of impaired central pain modulation in Parkinson's disease (PD) patients using laser‐evoked potential habituation and quantitative sensory testing. PD patients exhibited reduced habituation to painful stimuli, independent of reported pain or medication.
Dilara Kersebaum   +10 more
wiley   +1 more source

Multiregional blood-brain barrier phenotyping identifies the prefrontal cortex as the most vulnerable region to ageing in mice. [PDF]

open access: yesBrain Commun
Bravo-Ferrer I   +6 more
europepmc   +1 more source

Combined Dysfunction of the Amygdala and Nucleus Basalis Underlies Visual Hallucinations in Parkinson's Disease

open access: yesMovement Disorders, EarlyView.
Abstract Background Visual hallucinations (VHs) are a common feature of Parkinson's disease (PD) believed to arise from disruptions to the functional architecture supporting sensory integration and attentional control. Across synucleinopathies, increased pathological burden in the amygdala and deficits in cholinergic modulation have been linked to VHs.
Anna Ignatavicius   +6 more
wiley   +1 more source

Bayesian inference by visuomotor neurons in the prefrontal cortex. [PDF]

open access: yesProc Natl Acad Sci U S A
Langlois TA, Charlton JA, Goris RLT.
europepmc   +1 more source

Does COMT Play a Role in Parkinson's Disease Susceptibility across Diverse Ancestral Populations?

open access: yesMovement Disorders, EarlyView.
Abstract Background The catechol‐O‐methyltransferase (COMT) gene is involved in brain catecholamine metabolism, but its association with Parkinson's disease (PD) risk remains unclear. Objective Our aim was to investigate the relationship between COMT genetic variants and PD risk across diverse ancestries.
Miguel Martín‐Bórnez   +16 more
wiley   +1 more source

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