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Multiple System Atrophy

2005
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder that usually manifests in the early fifties and progresses relentlessly with a mean survival of 9 years. Clinically, MSA is dominated by autonomic/urogenital failure which may be associated with either levodopa unresponsive parkinsonism in 80p.cent of cases (MSA-P subtype) or with ...
G K, Wenning, F, Geser
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Progressive cerebral atrophy in multiple system atrophy

Journal of the Neurological Sciences, 2002
Nine patients with multiple system atrophy (MSA) were studied based on MRI findings of cerebral hemispheric involvement. The age at onset was 56.4+/-8.6 (mean+/-S.D.) years, duration of illness at the first MRI study 2.1+/-1.1 years, duration of illness at the last study 9.7+/-2.6 years, and the follow-up duration 7.6+/-2.3 years.
Masaaki, Konagaya   +4 more
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Survival in multiple system atrophy

Movement Disorders, 2008
AbstractWe here report survival in patients with multiple system atrophy (MSA) in a large, prospectively studied group of patients with MSA. Eighty‐five of 100 patients were known to have died. Three patients were rediagnosed as having PD. Twenty‐four patients came to autopsy, which showed MSA in 22 and idiopathic Parkinson's disease in 2.
Anette, Schrag   +3 more
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Pain in multiple system atrophy

Journal of Neurology, 1996
Pain is a recognized feature of idiopathic Parkinson's disease (IPD) but has never been studied in multiple system atrophy (MSA), the commonest cause of atypical parkinsonism. We retrospectively analysed histories of pain in 100 consecutive cases of clinically probable MSA.
F, Tison   +5 more
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Young-onset multiple system atrophy

Journal of the Neurological Sciences, 2012
Han-Joon Kim   +2 more
exaly   +4 more sources

Multiple system atrophy

Current Opinion in Neurology, 1998
Although the precise definition of multiple system atrophy has been difficult, a recent consensus in diagnostic criteria for multiple system atrophy has been achieved. This should lead to progress in defining the underlying pathophysiology of the neuroendocrine, autonomic and motor deficits characteristic of multiple system atrophy.
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Multiple system atrophy: An update

Movement Disorders, 2003
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder that usually manifests in the early sixth decade of life and progresses relentlessly with a mean survival of 9 years. Clinically, MSA is dominated by autonomic/urogenital failure, which may be associated with either levodopa (L-dopa) -unresponsive parkinsonism in 80% of cases (MSA-P
Gregor K, Wenning   +3 more
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Multiple system atrophy

2007
Publisher Summary This chapter deals with the epidemiology, clinical features, pathological characteristics, diagnostic evaluation, and treatment approaches for multiple system atrophy (MSA). MSA is regarded as a distinct disease process with a complex combination of clinical presentations.
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Sleep Dysfunction in Multiple System Atrophy

Current Treatment Options in Neurology, 2012
Sleep disorders in multiple system atrophy (MSA) are common manifestation and include reduced and fragmented sleep, excessive daytime sleepiness, REM sleep behaviour disorder (RBD), and sleep-disordered breathing. Of these, RBD is the most common (affecting 90 %-100 % of patients with MSA) and is regarded as a red flag for MSA.
FERINI STRAMBI , LUIGI, Marelli S.
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An update on multiple system atrophy

Current Opinion in Neurology
Purpose of review Multiple system atrophy (MSA) is a rapidly progressive synucleinopathy characterized by autonomic failure, parkinsonism, and cerebellar ataxia. Here, we provide an update on α-synuclein's role in MSA pathophysiology and review the new Movement Disorders Society (MDS) diagnostic criteria and the utility of α ...
Iva, Stankovic   +2 more
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