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Striatonigral Degeneration

Known as: Atrophy, Striatonigral, Striatonigral Degenerations, Atrophies, Striatonigral 
A sporadic neurodegenerative disease with onset in middle-age characterized clinically by Parkinsonian features (e.g., MUSCLE RIGIDITY; HYPOKINESIA… 
National Institutes of Health

Papers overview

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2005
2005
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder characterized by various combinations of parkinsonism… 
2004
2004
SummaryThe basal ganglia (including substantia nigra) of two patients with striatonigral degeneration, who had clinical histories… 
2004
2004
An autopsy was performed on a 48-year-old woman with clinical features of parkinsonism-plus syndrome with dominating akinesia… 
2001
2001
A 43-year-old woman had cogwheel rigidity, bradykinesia, bowel/bladder retention, and tongue tremor (levodopa-nonresponsive… 
2001
2001
Reply to “Overstimulation of the α 1B -adrenergic receptor causes a “seizure plus” syndrome” 
1999
1999
Our aim was to revisit the papers published by Scherer 1933 describing four cases of sporadic olivopontocerebellar atrophy (OPCA… 
1998
1998
Reported neurologic sequelae of electrical injury include hemiparesis, cerebellar atrophy, paraparesis, and a progressive motor… 
1995
1995
We present an autopsied case of striatonigral degeneration (SND) combined with olivopontocerebellar atrophy (OPCA) with… 
1988
1988
A case of probable neuroleptic malignant syndrome (NMS) complicating l-dopa withdrawal in striatonigral degeneration is described… 
1982
1982
In the regional distribution of I-3H-quinuclindinyl benzilate (3H-QNB) binding in human brains of neurologically unaffected cases…