A multimodal approach for diagnosis of early Multiple System Atrophy (MSA)
Objective: To describe the use of neuroimaging and fluid biomarkers to improve the diagnostic accuracy of early MSA. Background: The diagnosis of early MSA is…Investigation of usefulness of new MSA diagnostic criteria
Objective: We investigated the utility of the Movement Disorder Society Criteria (MDS criteria) including sensitivity and specificity. Background: Multiple system atrophy (MSA) is an adult-onset…Data-driven subtypes of multiple system atrophy and the implication on prognosis
Objective: To determine the clinical subtypes of MSA using data-driven approach and to compare the differences of the subtypes on survival and bed-ridden rates. Background:…Laryngeal clinical biomarkers in atypical Parkinsonism – results from an international multicenter study
Objective: To investigate the prevalence of laryngeal motion abnormalities in patients with atypical Parkinsonism. Background: Using a previously published FEES task-protocol[1-3], we identified irregular involuntary…LRRK2 G2019S mutation in Multiple System Atrophy, a case report
Objective: Presenting a case of Multiple System Atrophy (MSA) confirmed by skin biopsy with a peculiar genetic profile. Background: MSA is a rare neurodegenerative disorder characterized…The diagnostic utility of the new MDS criteria for multiple system atrophy: a retrospective autopsy cohort study
Objective: This study aimed to validate the clinical utility of the newly proposed criteria for multiple system atrophy (MSA) by the International Parkinson and Movement…Short-term effect of continuous positive airway pressure in MSA patients with sleep disordered breathing
Objective: SBD are frequent in MSA, mainly represented by inspiratory stridor, obstructive and central sleep apnea/hypopnea syndrome (SAS), or hypopneaimpacting the quality of sleep. A…Spinocerebellar Ataxia Autosomal Recessive Type 10 Misdiagnosed as a Multiple System Atrophy Type C: a Case Report.
Objective: Spinocerebellar ataxia autosomal recessive type 10 (SCAR 10) is a very rare cause of slowly progressive cerebellar ataxia caused by mutations of ANO10 gene…Pain in people with multiple system atrophy
Objective: To estimate prevalence of pain in people with multiple system atrophy (MSA).To estimate prevalence of pain in people with multiple system atrophy (MSA). Background:…Blood Pressure Monitoring in Multiple System Atrophy: Focused on Nocturnal Dipping Pattern
Objective: To depict 24 hour blood pressure profile, especially dipping patterns, in subjects with probable and clinically established multiple system atrophy (MSA). Background: Impairment of…
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