Results 41 to 50 of about 216,096 (151)
Heredity in multiple system atrophy [PDF]
Journal of the Neurological Sciences, 2006 We investigated the family histories of 157 Japanese patients with probable or possible multiple system atrophy (MSA). A family history of neurodegenerative disorders was only detected in three MSA patients (1.9%). We evaluated these patients by careful neurological examination, neuroimaging studies, and genetic studies to exclude hereditary ...
Soma, Hiroyuki +5 more
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Multiple system atrophy and autophagy
Rinsho Shinkeigaku, 2014 Macroautophagy is a dynamic process whereby cytoplasmic molecules are sequestered within autophagosomes. There exist two groups of mammalian autophagy-related gene (Atg) 8 homologues (LC3 and GABARAPs), which play essential role in autophagosomal formation.
Koichi, Wakabayashi, Kunikazu, Tanji
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Pareidolia in Parkinson’s Disease and Multiple System Atrophy
Parkinson's Disease, 2021 Pareidolia is a visual illusion of meaningful objects that arise from ambiguous forms embedded in visual scenes. Previous studies showed that pareidolias are frequently observed in patients with Parkinson’s disease (PD) as well as dementia with Lewy ...
Kentaro Kurumada +8 more
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Medullary microvessel degeneration in multiple system atrophy
Neurobiology of Disease, 2007 Multiple system atrophy (MSA) is a rare and fatal early-onset autonomic disorder which is characterised by Parkinsonism and orthostatic hypotension (OH).
V.M. Miller +4 more
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, 2019 Multiple system atrophy (MSA) is a sporadic, adult-onset, relentlessly progressive neurodegenerative disorder, clinically characterized by various combinations of autonomic failure, parkinsonism and ataxia. The neuropathological hallmark of MSA are glial cytoplasmic inclusions consisting of misfolded α-synuclein.
Fanciulli, Alessandra +5 more
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, 2013 Multiple system atrophy (MSA) is a sporadic and fatal α-synuclein-linked oligodendrogliopathy manifesting with progressive autonomic failure, poorly levodopa-responsive parkinsonism, and cerebellar ataxia, in any combination. Here we review key aspects of MSA integrating important insights from rapidly emerging fields such as genetics, diagnostic work ...
Gregor K, Wenning, Florian, Krismer
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Acoustic Characteristics of Stridor in Multiple System Atrophy. [PDF]
PLoS ONE, 2016 Nocturnal stridor is a breathing disorder prevalent in patients with multiple system atrophy (MSA). An improved understanding of this breathing disorder is essential since nocturnal stridor carries a poor prognosis (an increased risk of sudden death). In
Dae Lim Koo +4 more
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Dermal and cardiac autonomic fiber involvement in Parkinson's disease and multiple system atrophy
Neurobiology of Disease, 2021 Pathological aggregates of alpha-synuclein in peripheral dermal nerve fibers can be detected in patients with idiopathic Parkinson's disease and multiple system atrophy.
Joachim Brumberg +8 more
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COGNITIVE PERFORMANCE IN MULTIPLE SYSTEM ATROPHY [PDF]
Brain, 1992 The cognitive performance of a group of patients with multiple system atrophy (MSA) of striato-nigral predominance was compared with that of age and IQ matched control subjects, using three tests sensitive to frontal lobe dysfunction and a battery sensitive to memory and learning deficits in Parkinson's disease and dementia of the Alzheimer type.
Robbins, T. W. +5 more
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Diagnostic challenges in multiple system atrophy
Neuropsychiatric Disease and Treatment, 2018 Diana Obelieniene,1 Sandra Bauzaite,1 Ilona Kulakiene,2 Evaldas Keleras,2 Indre Eitmonaite,3 Daiva Rastenyte1 1Department of Neurology, 2Department of Radiology, 3Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania Abstract ...
Obelieniene D +5 more
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