Results 241 to 250 of about 19,535 (297)

Defining the Rhythm: Developing a New Method to Describe Tremor and Myoclonus

open access: yesMovement Disorders, EarlyView.
Abstract Background The hallmark feature of tremor is rhythmicity, which can be quantified using power spectral density (PSD) analysis. However, tremor exhibits considerable variability, ranging from highly regular to more irregular patterns. Similarly, rhythmicity in myoclonus varies, but it typically manifests as arrhythmic jerks.
Anna Latorre   +6 more
wiley   +1 more source

Pregnancy, Delivery, and Neonatal Outcomes in Women with Tourette Syndrome or Chronic Tic Disorder

open access: yesMovement Disorders, EarlyView.
Abstract Background Adverse pregnancy and neonatal outcomes in women with Tourette syndrome or chronic tic disorder (TS/CTD) have not been systematically studied. This Swedish population‐based study investigated associations between maternal TS/CTD and pregnancy, delivery, and neonatal outcomes.
Neda Razaz, Lorena Fernández de la Cruz
wiley   +1 more source

RAB32‐Linked Parkinson's Disease: Deep Phenotyping, MDSGene Literature Review, and Application of SynNeurGe Criteria

open access: yesMovement Disorders, EarlyView.
Abstract Background The RAB32 p.Ser71Arg variant is a novel cause of monogenic Parkinson's disease (PD), for which detailed phenotypic information is currently scarce. Objectives Our aim was to clinically and biologically characterize individuals with PARK‐RAB32 to gain insights into genotype–phenotype relationships, disease severity, and underlying ...
Teresa Kleinz   +27 more
wiley   +1 more source

Reproducibility in contouring the neurovascular bundle for prostate cancer radiation therapy. [PDF]

open access: yesPract Radiat Oncol, 2018
Cassidy RJ   +10 more
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

Home - About - Disclaimer - Privacy