Rett syndrome (RTT) is a rare and severe neurological disorder mainly affecting females,
usually linked to methyl-CpG-binding protein 2 (MECP2) gene mutations. Manifestations of …

Background Autonomic dysfunctions are prevalent in several cerebellar disorders, but they
have not been systematically investigated in spinocerebellar ataxias (SCAs). Studies …

Progressive supranuclear palsy (PSP) is an atypical Parkinsonian disorder which results in
deterioration of motor and cognitive skills, including language disorders such as impaired …

Mild cognitive impairment (MCI) in multiple-system atrophy (MSA) patients is common but
remains poorly characterized, and the related factors are unclear. This retrospective study …

Cognitive impairment (CI), previously considered as a non-supporting feature of multiple
system atrophy (MSA), according to the second consensus criteria, is not uncommon in this …

Purpose Multiple system atrophy (MSA) is a rare neurodegenerative disease, often
presented with orthostatic hypotension (OH), which is a disabling symptom but has not been …

Objective To compare the neuropathology between two types of multiple system atrophy-
parkinsonism-predominant (MSA-P) and cerebellar ataxia-predominant (MSA-C) with …

Nervous system dysfunction is induced by the slow and cumulative loss of neuronal cells in
neurodegenerative disorders. The phrase refers to an extensive range of clinical diseases …

Cerebral Small Vessel Disease Is Associated with Motor, Cognitive, and Emotional Dysfunction
in Multiple System Atrophy - IOS Press You are viewing a javascript disabled version of the …

Background: Multiple system atrophy (MSA) is a rare and fatal neurodegenerative disease
whose diagnosis is particularly complex. Currently, the definite diagnosis of MSA requires …