striatonigral

striatonigral

 [stri″ah-to-ni´gral]
projecting from the corpus striatum to the substantia nigra.

stri·a·to·ni·gral

(strī'ă-tō-nī'grăl),
Referring to the efferent connection of the striatum with the substantia nigra.

striatonigral

/stri·a·to·ni·gral/ (stri″ah-to-ni´gr'l) projecting from the corpus striatum to the substantia nigra.

stri·a·to·ni·gral

(strī'ā-tō-nī'grăl)
Referring to the efferent connection of the striatum with the substantia nigra

striatonigral

projecting from the corpus striatum to the substantia nigra.

striatonigral degeneration
the basic lesion in hereditary striatonigral and cerebello-olivary degeneration in Kerry blue terriers. See also cerebellar abiotrophy.
References in periodicals archive ?
3 Formerly these were synonymous as sporadic olivopontocerebellar atrophy (sOPCA), striatonigral degeneration and Shy-Drager syndrome respectively.
Coordinated and spatial upregulation of arc in striatonigral neurons correlates with L-dopa-induced behavioral sensitization in dyskinetic rats.
Thin section MR study of the basal ganglia in the differential diagnosis between striatonigral degeneration and parkinson disease.
Matsushita, "The distribution and dynamic density of oligodendroglial cytoplasmic inclusions (GCIs) in multiple system atrophy: a correlation between the density of GCIs and the degree of involvement of striatonigral and olivopontocerebellar systems," Acta Neuropathologica, vol.
parkinsonian type (MSA-P), characterized by striatonigral degeneration and increased spasticity
The diagnosis for probable MSA was performed by a neurologist through magnetic resonance imaging and confirmed by the predominant striatonigral degeneration in the absence of cerebellar dysfunction, presence of cardinal features including parkinsonism, and symptoms of autonomic failure (Quinn and Wenning, 1996).
It regulates the striatonigral neurons via D1-dopamine receptors but regulates the striatopallidal neurons via D2-dopamine receptors [19].
Different responsiveness of striatonigral and striatopallidal neurons to L-Dopa after a subchronic intermittent L-Dopa treatment.
Striatal D2 receptor status in patients with Parkinson's disease, striatonigral degeneration, and progressive supranuclear palsy measured with 11C-raclopride and positron emission tomography.
It has been documented that DA from substantia nigra neurons excites striatonigral neurons, while another neurotransmitter, acetylcholine (ACh) from striatal cholinergic neurons, opposing DA action, inhibits striatonigral neurons (12).
MSA was originally divided into Shy-Drager syndrome, striatonigral degeneration, and olivopontocerebellar atrophy, but this distinction is no longer made.
The striatonigral degenerations, putaminal pigments and nosology.