Results 261 to 270 of about 80,208 (340)

Not So Smooth Sailing: FIG4‐Related Disease Is a Differential Diagnosis of Rapid Onset Dystonia‐Parkinsonism

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Matthew Julian Georgiades   +7 more
wiley   +1 more source

Long‐Term Safety and Efficacy of Repeat Treatments with DaxibotulinumtoxinA in Cervical Dystonia: Results from the ASPEN‐Open‐Label Study

open access: yesMovement Disorders Clinical Practice, EarlyView.
ABSTRACT Background DaxibotulinumtoxinA (DAXI), a novel botulinum neurotoxin (BoNT) formulation, was shown to be safe, effective, and long‐lasting in the treatment of cervical dystonia (CD) over one treatment cycle in the phase 3, randomized, placebo‐controlled ASPEN‐1 trial.
Peter McAllister   +11 more
wiley   +1 more source

Adult‐Onset Dystonia‐Parkinsonism: Do Not Forget SERAC1

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Giulia Scacciatella   +15 more
wiley   +1 more source

Functional Connectivity and Volumetrics Improve Outcome Prediction for Deep Brain Stimulation in Parkinson's Disease

open access: yesMovement Disorders Clinical Practice, EarlyView.
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

Therapeutic Potential of Agmatine in Essential Tremor Through Regulation of Lingo-1 and Inflammatory Pathways. [PDF]

open access: yesBrain Behav
Pirmoradi Z   +6 more
europepmc   +1 more source

Deep Brain Stimulation Improves Symptoms in an Individual with Alpha‐Synuclein‐Gene‐Associated Parkinson's Disease

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Abigail Braun   +5 more
wiley   +1 more source

Hereditary Spastic Paraplegia in Alberta: Lessons from a Well‐Defined Cohort Including the Indigenous Population

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Hereditary spastic paraplegias (HSP) are rare disorders sharing common features of leg spasticity with gait impairment. Simple and complex forms are recognized; over 50% of cases remain unsolved genetically. Little is known about the genetics of HSP among Indigenous Peoples. Objectives To describe clinical, radiological, and genetic
Ekhlas Assaedi   +7 more
wiley   +1 more source

Essential tremor plus affects disease prognosis: A longitudinal study. [PDF]

open access: yesChin Med J (Engl)
He R   +13 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy