Results 291 to 300 of about 13,498,406 (368)
Abstract Background Deep brain stimulation (DBS) targeting the subthalamic nucleus (STN) can effectively treat motor symptoms of Parkinson's disease (PD). However, optimal patient selection remains challenging due to the inadequacy of outcome predictors.
John R. Younce+3 more
wiley +1 more source
The Effectiveness of Training Programs on the Fidelity of Neuropsychological Tests. [PDF]
Takeda S+5 more
europepmc +1 more source
Editorial: Neuropsychological testing: from psychometrics to clinical neuropsychology
Alessio Facchin+2 more
openaire +3 more sources
Rare GNAO1 Variant Presenting with Deep Brain Stimulation‐Responsive Jaw‐Opening Dystonia
Movement Disorders Clinical Practice, EarlyView.
Fabian Maass+4 more
wiley +1 more source
Does Right‐Hand Motor Impairment Affect Performance on Cognitive Testing in Parkinson's Disease?
ABSTRACT Background For People with Parkinson's (PwP), motor disturbances affecting the dominant upper extremity often impacts ability to perform tasks such as writing or typing and may confound cognitive test performances with graphomotor responding. Objectives We explored association between upper extremity impairment and graphomotor cognitive test ...
Priyanka Rao+2 more
wiley +1 more source
Adult‐Onset Dystonia‐Parkinsonism: Do Not Forget SERAC1
Movement Disorders Clinical Practice, EarlyView.
Giulia Scacciatella+15 more
wiley +1 more source
Micrographia in Parkinson's Disease: Automatic Recognition through Artificial Intelligence
Abstract Background Parkinson's disease (PD) leads to handwriting abnormalities primarily characterized by micrographia. Whether micrographia manifests early in PD, worsens throughout the disease, and lastly responds to L‐Dopa is still under scientific debate.
Francesco Asci+8 more
wiley +1 more source
Cognitive Changes in Pre‐ataxic Spinocerebellar Ataxias: A Scoping Review
Abstract Background Although traditionally recognized for motor impairment, evidence suggests that cognitive deficits may emerge before ataxia onset in autosomal dominant spinocerebellar ataxias (SCA), particularly in nucleotide repeat expansion SCAs (NRE‐SCAs).
Renata Barreto Tenorio+3 more
wiley +1 more source