Education in hyperkinetic movement disorders in Cameroonian health providers
Objective: To evaluate the educational gaps in hyperkinetic movement disorders among a widely-varied sample of Cameroonian health providers and improve understanding through a practical training…Malignant gliomas in patients with Huntington’s disease
Objective: Discuss the presentation of glioblastoma multiforme in patients with Huntington’s disease Background: Huntington’s disease (HD) is an inherited neurodegenerative disorder caused by a trinucleotide…The History of Huntington Disease Description in Russia
Objective: The report provides detailed material on the history of the description of Huntington's disease (HD) in Russia. The first, unknown to a wide audience,…Assessing the potential of EEG as a biomarker in Huntington’s disease using machine learning automatic classification
Objective: To construct an automatic classifier distinguishing healthy controls from Huntington’s disease (HD) gene carriers using quantitative electroencephalography (qEEG) and to derive qEEG features that…Generalized choreoathetoid-like movements in primary Sjögren syndrome
Objective: To report a case of choreoathetoid-like movements associated to primary Sjögren syndrome. Background: Autoimmune diseases are not uncommon causes of movement disorders. Two percent…Late onset Huntington’s disease in an Argentinian cohort
Objective: To describe the prevalence, clinical and molecular characteristics of a series of LOHD patients in an Argentinean cohort. Background: Late onset Huntington’s disease (LOHD)…Sydenham’s Chorea: Realities and Challenges in Sub-Saharan Africa
Objective: The aim of this study was to describe the epidemiological, clinical, paraclinical and evolutive aspects of Sydenham's chorea. Background: Sydenham's chorea is a rare…On the hunt for a link between genetically confirmed Huntington’s disease and Amyotrophic Lateral Sclerosis
Objective: To characterise the clinical and pathologic findings of Huntington’s disease (HD) and coincident amyotrophic lateral sclerosis (ALS). Background: A 66 year old man presented…Spinocerebellar Ataxia Type 2 Presenting with Chorea: Korean Cases
Objective: To report cases of SCA2 presenting with chorea, which have not been reported in Korea Background: Spinocerebellar ataxias (SCAs) manifest ethnic and geographical differences…Commonalities of prodromal non-motor symptoms between movement disorders
Objective: This study reviewed and compared evidence of nonmotor symptoms in prodromal phases in movement disorders including Parkinson disease, Atypical Parkinsonism (MSA, DLB, PSP), Huntington…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.