Results 301 to 310 of about 354,264 (324)
Some of the next articles are maybe not open access.
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.
openaire +2 more sources
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.
openaire +2 more sources
Journal of the Neurological Sciences, 1974
Abstract The 5 familial cases which are reported here, showed a similar clinical course characterized by an early onset and a very long duration provided adequate nursing care was available. The main features were a very prominent pyramidal syndrome, less pronounced or partially masked cerebellar, myoclonic and extrapyramidal syndromes and ...
J.J. Martin +4 more
openaire +1 more source
Abstract The 5 familial cases which are reported here, showed a similar clinical course characterized by an early onset and a very long duration provided adequate nursing care was available. The main features were a very prominent pyramidal syndrome, less pronounced or partially masked cerebellar, myoclonic and extrapyramidal syndromes and ...
J.J. Martin +4 more
openaire +1 more source
Reviews in neurological diseases, 2011
Multiple system atrophy (MSA) is an adult-onset, progressive, neurodegenerative condition that has several different initial presentations. Ultimately affected patients develop parkinsonian features, autonomic dysfunction, cerebellar ataxia, and corticospinal deficits. Patients with MSA are often misdiagnosed as having Parkinson disease.
Jason S, Hawley +2 more
openaire +1 more source
Multiple system atrophy (MSA) is an adult-onset, progressive, neurodegenerative condition that has several different initial presentations. Ultimately affected patients develop parkinsonian features, autonomic dysfunction, cerebellar ataxia, and corticospinal deficits. Patients with MSA are often misdiagnosed as having Parkinson disease.
Jason S, Hawley +2 more
openaire +1 more source
Implanted System for Orthostatic Hypotension in Multiple-System Atrophy
New England Journal of Medicine, 2022Jordan W Squair +2 more
exaly
Discriminating α-synuclein strains in Parkinson’s disease and multiple system atrophy
Nature, 2020Mohammad Shahnawaz +2 more
exaly
Structures of α-synuclein filaments from multiple system atrophy
Nature, 2020Manuel Schweighauser +2 more
exaly