Oculopalatal myoclonus after stroke
Objective: Analysis of clinical course of oculopalatal myoclonus (OPM) and MRI images of the brain. Background: OPM are rare movement disorders connected with the injury…Depression and apathy in restless legs syndrome
Objective: We examined the prevalence of mood disorders (depression, apathy) and its' characteristics. Moreover, to investigate pathophysiology of the mood disorders in the patient in…Relationship of serum ferritin level and tic severity in children with Tourette syndrome
Objective: Evaluate the relationship between serum ferritin levels and tic severity, as well as consequent impact on life, in children with Tourette Syndrome. Background: There…Orthostatic tremor: Disease progression and disability
Objective: To develop a questionnaire quantifying the impact of orthostatic tremor (OT) on function and quality of life to enable some measure of disease severity…Nystagmus in harmaline induced tremors in rats and attenuation with ethanol
Objective: To study nystagmus in harmaline induced tremor (HIT) in rats. Background: Clinical observations have shown the presence of nystagmus in some patients with essential…ICF-based effects of VIM-DBS on communication in everyday life in patients with essential tremor
Objective: The aim of the study was to determine how patients with essential tremor (ET) evaluate the functional, physical and emotional effects of VIM-DBS on…Olfaction analysis in spinocerebellar ataxia type 10 and type 3 comparing with healthy controls and PD
Objective: To Analyse olfaction in spinocerebellar ataxia type 10 and type 3. Background: The main clinical manifestations of spinocerebellar ataxias (SCA) result from the involvement…Peripheral insulin sensitivity and body composition alterations in early stage Machado Joseph disease
Objective: To describe body composition and peripheral sensitivity to insulin (PSI) in early stage and presymptomatic spinocerebellar ataxia type 3/Machado Joseph disease (SCA3/MJD) individuals and…Predominant motor neuron involvement in autosomal recessive SYNE1 ataxia
Objective: We here report on a novel SYNE1 mutation in an Austrian family extending the classical clinical phenotype in SYNE1 ataxia. Background: SYNE1 codes for…A novel causal mutation for spinocerebellar ataxia 19/22 (SCA19)
Objective: We report a novel cause for SCA19. We obtained longitudinal exam data on the index case, and data on other family members. We conducted…
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