A new mutation in the C-terminal domain of the YY1 gene associated with Gabriele-de Vries syndrome.
Objective: To report a new mutation in the YY1 gene in a patient with Gabriele-de Vries syndrome, in which dystonia and choreoathetosis were the most…Botulinum injections for idiopathic cervical dystonia: a longitudinal study
Objective: In this retrospective longitudinal study, we explored the efficacy of repeated BT injection sessions for idiopathic cervical dystonia (ICD). Background: Botulinum toxin (BT) injections…Preliminary validation of an educational handbook for Parkinson’s disease patients in Brazil
Objective: To describe the development and preliminary validation of an educational handbook for Parkinson’s disease (PD) patients. Background: PD is a progressive, chronic and heterogeneous…Clinical and Economic Outcomes Associated with Dysphagia in Hospitalized Patients with Parkinson’s Disease
Objective: To evaluate the outcomes associated with dysphagia in hospitalized patients with Parkinson's Disease and associated healthcare costs and utilization. Background: Dysphagia in Parkinson's Disease…Reproductive factors and risk of Parkinson’s disease in women: preliminary results from the French prospective cohort E3N.
Objective: Objective: To evaluate whether reproductive factors and use of exogenous hormones are associated with the risk of Parkinson’s disease (PD) in women. Background: Background:…Intensive rehabilitation program for patients with functional motor disorders: 3-years’ experience.
Objective: To describe the clinical characteristics and the outcomes of a cohort of patients with functional movement disorders (FMD) who attended the FMD clinic of…Neural oscillations modulation during working memory in premanifest and early Huntington’s disease
Objective: To test whether high-density electroencephalography (hdEEG) coupled to source localization allows for the identification of neuronal oscillations in specific frequency bands in patients with…Atypical gait in a patient with Huntington’s Disease (HD): Functional movement disorders in the spectrum of motor phenotypes in HD
Objective: We describe a case of Huntington’s disease (HD) associated chorea and concurrent functional movement disorder (FMD). Background: HD is a neurodegenerative disorder characterized by…Validation of biomarkers in Huntington’s disease to support the development of disease-modifying therapies: a systematic review and critical appraisal scheme
Objective: To review studies for disease progression biomarkers published in HD and evaluate their methodological quality in a standardized manner. Background: Huntington disease (HD) is a fatal autosomal dominant neurodegenerative condition that starts to manifest clinically around the 4th decade of life. There are promising novel genetic-based therapies under development intended to modify the disease trajectory. Valid…Neural correlates of executed compared to imagined writing and drawing movements. An fMRI study
Objective: In this study we used functional magnetic resonance imaging (fMRI) to investigate whether motor imagery (MI) of handwriting and circle drawing activates a similar…
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