Results 11 to 20 of about 1,668 (203)

A case of multiple system atrophy [PDF]

open access: yesJournal of International Medical Research, 2019
Multiple system atrophy (MSA) is the most rapidly progressive neurodegenerative disorder among the various types of synucleinopathies. The cause of MSA remains unknown, but it can involve the extrapyramidal system, the pyramidal system, the autonomic ...
Jing Guo   +4 more
doaj   +3 more sources

Tremor in Multiple System Atrophy - a review

open access: yesTremor and Other Hyperkinetic Movements, 2013
Background: Multiple system atrophy (MSA) is a rare neurodegenerative movement disorder characterized by a rapidly progressive course. The clinical presentation can include autonomic failure, parkinsonism, and cerebellar signs.
Christine Kaindlstorfer   +2 more
doaj   +5 more sources

MULTIPLE SYSTEM ATROPHY [PDF]

open access: yesMedical Clinics of North America, 1999
MSA is a complex disorder, with regard to its pathology and cause as well as its clinical diagnosis and treatment. Although a number of clinical treatments may improve quality of life for these patients, given the widespread pathology present, symptomatic treatment, particularly that involving neurotransmitter replacement, is likely to remain difficult.
L, Swan, J, Dupont
  +7 more sources

Multiple System Atrophy [PDF]

open access: yesSeminars in Neurology, 2001
Multiple system atrophy (MSA) is an adult-onset sporadic progressive neurodegenerative disorder of unknown etiology. It is clinically characterized by the variable combination of autonomic failure, parkinsonism, cerebellar ataxia, and pyramidal signs. The present review summarizes up-to-date knowledge on the clinical diagnosis and molecular pathology ...
G K, Wenning   +4 more
  +7 more sources

Multiple system atrophy

open access: yesS.S. Korsakov Journal of Neurology and Psychiatry, 2023
The article presents a progressive neurodegenerative disease — multisystem atrophy, characterized by a combination of autonomic failure and various motor disorders, including parkinsonism and/or cerebellar ataxia; etiopathogenetic factors and variants of the clinical picture are described.
M.P. Topuzova   +8 more
openaire   +5 more sources

The genetic basis of multiple system atrophy

open access: yesJournal of Translational Medicine, 2023
Multiple system atrophy (MSA) is a heterogenous, uniformly fatal neurodegenerative ɑ-synucleinopathy. Patients present with varying degrees of dysautonomia, parkinsonism, cerebellar dysfunction, and corticospinal degeneration.
Fan Shuen Tseng   +3 more
doaj   +1 more source

Multiple Sistem Atrophy: Sebuah Laporan Kasus

open access: yesAksona, 2021
Pendahuluan: Multiple sistem atrophy adalah penyakit degeneratif yang dapat menyebabkan kecacatan bahkan kematian. Sedikit jurnal yang yang membahas tentang diagnosis dan penanganan multiple system atrophy secara menyeluruh.
Edfina Rahmarini   +4 more
doaj   +1 more source

Models of multiple system atrophy [PDF]

open access: yesExperimental & Molecular Medicine, 2019
AbstractMultiple system atrophy (MSA) is a neurodegenerative disease with diverse clinical manifestations, including parkinsonism, cerebellar syndrome, and autonomic failure. Pathologically, MSA is characterized by glial cytoplasmic inclusions in oligodendrocytes, which contain fibrillary forms of α-synuclein.
Lee, He-Jin   +3 more
openaire   +2 more sources

Multiple system atrophy-cerebellar: A case report and literature review

open access: yesRadiology Case Reports, 2023
We reported a case of a 48-year-old female patient admitted to the hospital due to balance disorder which progressed rapidly within 1 week. Cerebral magnetic resonance imaging showed significant atrophy and hyperintensities at the middle cerebellar ...
Thi Thuong Doan, MD   +5 more
doaj   +1 more source

Pan-American Consortium of Multiple System Atrophy (PANMSA). A Pan-American multicentre cohort study of Multiple System Atrophy

open access: yesJournal of Parkinson’s Disease, 2014
Background: Multiple system atrophy (MSA) is an adult-onset and rapidly progressive, neurodegenerative condition that presents with autonomic dysfunction, parkinsonism, cerebellar ataxia and corticospinal deficits.
Emilia Gatto   +15 more
doaj   +1 more source

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