Duodopa for the treatment of severe restless legs syndrome
Objective: To describe the outcome of a patient with restless legs syndrome (RLS) and augmentation phenomena that was treated with Duodopa in continuous infusion. Background:…Medical cannabis for the treatment of Tourette syndrome: A descriptive analysis of 24 patients
Objective: To assess the subjective effects of medical cannabis (MC) on patients with multiple treatment-resistant Tourette syndrome (TS). Background: Several single case studies and two…Neurodegenerative disorders with atypical course and cause, diagnostic contribution of genetics and magnetic resonance imaging, two case reports
Objective: We present two case reports – the first patient originally diagnosed with typical essential tremor and the second one with high suspicion on spinocerebellar…Post-traumatic rubral tremor – A rare entity
Objective: Tremor may be caused by trauma to the central and peripheral nervous systems. Although brain and nerve injuries are common, post traumatic tremor is…The effect of uni- and bilateral thalamic deep brain stimulation on speech in patients with essential tremor: Acoustics and intelligibility
Objective: In this study, we investigate the effect of VIM-DBS on speech in ET patients. We compare how uni- vs. bilateral DBS contributes to the…Esophageal involvement in multiple system atrophy
Objective: To determine the prevalence of esophageal involvement and its impact on clinical manifestations in patients with multiple system atrophy (MSA). Background: Secondary motor disorders…Magnetic resonance imaging in spinocerebellar ataxias: A systematic review
Objective: To perform a systematic review about quantitative central nervous system (CNS) magnetic resonance imaging (MRI) techniques findings in patients with Polyglutamine expansion (PolyQ) spinocerebellar…Co-occurrence of two triplet repeat associated SCA mutations: A dilemma in clinical diagnosis, prognosis and genetic counselling and clinical significance
Objective: To report clinical and genetic outcomes of rare combinatiorial triplet repeat expansion(TRE), SCA mutations in patients. Background: The presence of more than one TRE-SCA…Neurologic phenotipic variability in spinocerebelar ataxia hype 2 (SCA2)
Objective: Describe the clinical findings of a Brazilian cohort of SCA2 patients, stratify them according the presence of sub-phenotypes: cognitive deterioration, sensory loss, amiotrophy, parkinsonism…Huntington disease phenocopies or misdiagnosis: A black South African cohort
Objective: To investigate the occurrence of phenocopy mutations in a cohort of black South African individuals referred to the National Health Laboratory Service (NHLS) for…
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