2000
DOI: 10.1002/1531-8257(200007)15:4<699::aid-mds1015>3.0.co;2-l
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Stridor and death in multiple system atrophy

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Cited by 205 publications
(122 citation statements)
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References 22 publications
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“…There are a few recent reports on RBD associated with spinocerebellar atrophy type 3 (Machado-Joseph disease). [63][64][65] As noted above, numerous cases of RBD have been reported in conjunction with MSA, 3,22,23,27,[66][67][68][69][70][71][72] PD, 3,11,22,[24][25][26][27][30][31][32][33][34][35]73 and DLB. 1,10,15,41,45,[47][48][49][50][51][52][53]55,59,60,74 Although frequency data on the presence of RSWA and RBD in the neurodegenerative disorders is based on relatively small numbers of patients thus far, the presence of each in MSA has been reported to be 90% to 95% for RSWA and 68% to 90% for RBD, 66,67 and presence of each in PD is approximately 58% for RSWA and 33% for RBD.…”
Section: The Rbd-synucleinopathy Associationmentioning
confidence: 99%
“…There are a few recent reports on RBD associated with spinocerebellar atrophy type 3 (Machado-Joseph disease). [63][64][65] As noted above, numerous cases of RBD have been reported in conjunction with MSA, 3,22,23,27,[66][67][68][69][70][71][72] PD, 3,11,22,[24][25][26][27][30][31][32][33][34][35]73 and DLB. 1,10,15,41,45,[47][48][49][50][51][52][53]55,59,60,74 Although frequency data on the presence of RSWA and RBD in the neurodegenerative disorders is based on relatively small numbers of patients thus far, the presence of each in MSA has been reported to be 90% to 95% for RSWA and 68% to 90% for RBD, 66,67 and presence of each in PD is approximately 58% for RSWA and 33% for RBD.…”
Section: The Rbd-synucleinopathy Associationmentioning
confidence: 99%
“…Parkinsonism is defined by the presence of two of three symptoms, including rigidity, tremor, and hypokinesia. The most common atypical form of parkinsonism, multiple system atrophy (MSA), is a relentlessly progressive neurodegenerative disorder characterized by neuronal cell loss and gliosis in specific areas of the brain, causing various combinations of systemic degeneration [3,4]. Although it is well known that these two disease entities have different underlying mechanisms, including studies of potential causal factors, differential diagnosis of parkinsonian disorders on the basis of clinical signs and symptoms is still difficult due to overlapping symptomatology.…”
Section: Introductionmentioning
confidence: 99%
“…Cases of sudden death during sleep have still been reported following treatment with either nasal CPAP or tracheostomy, suggesting that other mechanisms of autonomic dysfunction may still be fatal in MSA. 4,6 RBD and REM sleep without atonia characterized by especially prominent excessive tonic muscle activity are frequent in MSA. Melatonin or clonazepam may be offered as therapies, with melatonin preferred to avoid exacerbating SDB and neurological dysfunction.…”
Section: -4mentioning
confidence: 99%