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… (More)
National Institutes of Health

Papers overview

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Highly Cited
2004
Highly Cited
2004
Multiple system atrophy (MSA) has varying clinical (MSA-P versus MSA-C) and pathological [striatonigral degeneration (SND) versus… (More)
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Highly Cited
1998
Highly Cited
1998
Iodine-123 meta-iodobenzylguanidine ([123I]MIBG), an analogue of norepinephrine, is a tracer for functioning of sympathetic… (More)
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Highly Cited
1996
Highly Cited
1996
We report longitudinal data on a group of 29 male patients 50 years of age or older who were initially diagnosed as having… (More)
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1993
1993
Regional and global metabolic rates for glucose were estimated using 18F-fluorodeoxyglucose and positron emission tomography in… (More)
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Highly Cited
1992
Highly Cited
1992
Equilibrium striatal: cerebellar 11C-raclopride (RAC) uptake ratios reflect the density of striatal dopamine D2 binding sites… (More)
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Highly Cited
1991
Highly Cited
1991
The micro-architecture of the substantia nigra was studied in control cases of varying age and patients with parkinsonism. A… (More)
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Highly Cited
1990
Highly Cited
1990
The clinical and pathological features of 10 cases of striatonigral degeneration are described: 5 were misdiagnosed in life as… (More)
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Highly Cited
1989
Highly Cited
1989
Glial cytoplasmic inclusions (GCIs) were demonstrated by silver staining, immunocytochemistry and by electron microscopy in the… (More)
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Highly Cited
1978
Highly Cited
1978
We studied 40 patients in 15 families from the Portuguese Azores Islands. Each family was affected by an autosomal dominant… (More)
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Highly Cited
1976
Highly Cited
1976
An autosomal dominant striatonigral degeneration is present in a family of Portuguese ancestry numbering in excess of 329 persons… (More)
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