Explicit movement control in functional movement disorders is characterized by reduced lateralized beta desynchronisation
Objective: To test whether beta power remains abnormally raised during motor preparation in functional movement disorders (FMD) patients. Background: Excessive attention towards movement control is…Plasma Biomarkers in Idiopathic Normal Pressure Hydrocephalus
Objective: (1) To investigate the role of plasma biomarkers that is known to related to Alzheimer’s disease in INPH(2) To assess the diagnostic and prognostic…Inhibition of long term memory and induction of biochemical deficits in rats following protofibrillar Aβ 1-42 injection
Objective: The present study was undertaken to study the effects of single intracerebroventricular (i.c.v.) injection of protofibrillar Aβ 1-42 on the long term memory Background:…Case study: Real-time MRI articulatory comparison of a congenital aglossic and normal speaker
Objective: Congenital aglossia is a rare syndrome of born without a tongue. This paper examines articulatory movements of a congenital aglossic speaker to understand physiology by…Multivariate analysis of writer`s cramp: a study with advanced multi-channel microelectrode recording system
Objective: To quantify difference in WC patients with Concordant mirror movements(MMs) from those with Discordant MMs. Background: Invasive methods are encouragive for quantitative analysis. The…Glut-1 deficiency: a case report
Objective: To report the case of a patient with refractory seizures who was diagnosed with Glut-1 deficiency. Background: Although Epilepsy is commonly diagnosed by child…Putaminal Atrophy Gradient in X-linked Dystonia-Parkinsonism
Objective: To better understand striatal pathology in X-linked Dystonia-Parkinsonism (XDP) by combining T1 and Magnetization Transfer (MT) Imaging. Background: XDP is a neurodegenerative disorder characterized by…Saccadic impairment in patients with Gaucher’s disease type 3
Objective: To characterize saccades in patients with chronic neuronopathic Gaucher’s disease (GD3) in relationship to their neurological and cognitive status using a computer-based eye-tracking technique. Background: GD3 is…Development of a Paroxysmal Movement Disorder Diary for Patients with Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)
Objective: To perform qualitative research to develop and establish content validity of a new clinical outcome assessment (COA) instrument for paroxysmal movement disorders in Glut1…Neurological worsening in patients undergoing treatment for Wilson disease: Frequency, causes and outcomes.
Objective: To study the pattern of neurological worsening (NW) in patients undergoing treatment for Wilson disease (WD). Background: WD is an inherited disorder of copper…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.