Results 241 to 250 of about 74,631 (338)
Abstract Background Breakdown of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) in basal ganglia cells through hydrolysis of diesteric bonds, primarily by PDE10A and PDE1B, is essential for normal human movement. While biallelic loss‐of‐function variants in PDE10A are known to cause hyperkinetic movement disorders, the ...
Tomer Poleg+21 more
wiley +1 more source
Reconsidering dopaminergic modulation in Alzheimer's disease: A case for levodopa/carbidopa as a disease-modifying agent. [PDF]
Nobili A, D'Amelio M.
europepmc +1 more source
A Convergent Pathway for Stimulation‐Induced Dyskinesia Following Deep Brain Stimulation
Abstract Background Stimulation‐induced dyskinesias (SID) from deep brain stimulation (DBS) of the subthalamic nucleus (STN) and globus pallidus internus (GPi) are uncommon; however, they are increasingly recognized. Once considered transient and indicative of effective neuromodulation, SID are now seen as potential therapy‐limiting side effects, akin ...
Joshua K. Wong+4 more
wiley +1 more source
Innovations in Parkinson's Disease: Strategies and Novel Technologies. [PDF]
Sha R+4 more
europepmc +1 more source
Adult‐Onset BPAN: An Atypical Presentation Mimicking Early‐Onset Parkinson's Disease
Movement Disorders Clinical Practice, EarlyView.
Mariana H.G. Monje+5 more
wiley +1 more source
Abstract Background High frequency deep brain stimulation of the subthalamic nucleus (STN‐DBS) is a well‐established therapy for Parkinson's disease (PD) motor symptoms, however, its effect on non‐motor symptoms is controversial. Low frequency DBS can improve cognition, but its effects on motor functions are detrimental.
Lucia Ricciardi+10 more
wiley +1 more source
Revamping Parkinson's disease therapy using PLGA-based drug delivery systems. [PDF]
Lababidi JM, Azzazy HME.
europepmc +1 more source
Abstract Traditionally, clinical trials of putative disease‐modifying therapies in Parkinson's disease have enrolled untreated patients at the earliest clinical stages of their disease. Due to a number of challenges inherent with this approach, there has been a recent move to a different study design, enrolling patients who are already taking “stable ...
M. Maral Mouradian+2 more
wiley +1 more source