Cerebellar structural covariance networks in young people with Tourette syndrome
Objective: To investigate discrete structural brain networks in children and adolescents with Tourette syndrome [TS] relative to a group of matched control participants. Background: TS…Efficacy and safety of CX-8998 in T-CALM, a randomized, double-blind, placebo-controlled, phase 2a trial in participants with essential tremor: subgroup analysis by baseline tremor severity
Objective: Evaluate efficacy and safety of CX-8998 in essential tremor (ET) as a function of baseline tremor severity. Background: CX-8998, a selective modulator of T-type…Essential tremor and essential tremor plus are essentially similar on electrophysiological tremor analysis
Objective: To compare the electrophysiological characteristics of tremor in subjects with Essential Tremor (ET) and Essential Tremor Plus (ET Plus). Background: Patients with neurological signs…Implementing a change of approach: From mono- to interdisciplinary follow-up of patients with PD
Objective: Evaluate the effect of a change of approach for allied healthcare professionals (AHP): From a mono- to interdisciplinary follow-up of patients with PD. Background:…Concurrent SCA3 and SCA10 in a young man with ataxia and prominent dystonia
Objective: To describe a case of a man with pathogenic repeat expansions in both ATXN3 and ATXN10. Background: SCA3 is caused by abnormal polyglutamine repeat…Whole exome sequencing in patients with undiagnosed ataxia in a Korean population
Objective: To investigate genetic causes of cerebellar ataxia in Korea using whole exome sequencing (WES) Background: Cerebellar ataxia encompasses a number of neurological conditions with…A Case Report of Spinocerebellar ataxia 13 with Parkinsonism
Objective: To present a Spinocerebellar Ataxia (SCA) 13 case who presented with parkinsonism with positive DatScan and good response to Levodopa. Background: Spinocerebellar ataxia (SCA)…Analysis of cases with Huntington’s disease phenotype and negative genetic test for huntingtin mutations in the Center for Movement Disorders (CETRAM) in Chile
Objective: To describe cases referred to CETRAM suspected of Huntington's disease (HD) according their phenotype, in whom an alternative diagnosis was proposed after ruling out…Low Educational Level and Wilson’s disease: A direct path to cognitive decline
Objective: To assess cognitive profile of Wilson's Disease (WD) patients in a single tertiary Movement Disorders center in Fortaleza, Ceará, Brazil. Background: WD is an autosomal recessive disorder…Abrogation of neuroinflammation and behavioural deficit by Chlorogenic acid and Tinosporia cordiofolia in MPTP-Induced Parkinsonian mice model via suppressing NF-κB pathway
Objective: The current study was designed with the aim to investigate the anti-neuroinflammatory activity of chlorogenic acid (CGA) and ethanolic extract of Tinospora cordifolia (TPE)…
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