Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Olivopontocerebellar Atrophies

Known as: Degeneration, Olivo-Ponto-Cerebellar, Degenerations, Olivo-Ponto-Cerebellar, Syndrome, Dejerine-Thomas 
A group of inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary… Expand
National Institutes of Health

Related topics

Related topics

30 relations
Ataxia, SpinocerebellarCentral Nervous SystemIchthyosis follicularis atrichia photophobia syndromeIn Blood
Expand

Narrower (14)

Familial Olivopontocerebellar AtrophyNonfamilial Olivopontocerebellar AtrophyOlivopontocerebellar Atrophy II, Autosomal RecessiveOlivopontocerebellar Atrophy V
Expand

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Expert consensus for multimodality imaging evaluation of adult patients during and after cancer therapy: a report from the American Society of Echocardiography and the European Association of…
### A. Definition, classification, and mechanisms of toxicity Cardiac dysfunction resulting from exposure to cancer therapeutics… Expand
  • table 1
  • table 2
  • figure 1
  • figure 2
  • figure 3
Highly Cited
2006
Highly Cited
2006
The value of the IUCN Red List for conservation.
The IUCN Red List of Threatened Species is the most comprehensive resource detailing the global conservation status of plants and… Expand
  • table 1
  • figure 1
Highly Cited
2005
Highly Cited
2005
On the unification power of models
  • J. Bézivin
  • Software & Systems Modeling
  • 2005
    • Corpus ID: 15449485
In November 2000, the OMG made public the MDA™initiative, a particular variant of a new global trend called MDE (Model Driven… Expand
  • figure 2
  • figure 3
  • figure 4
  • figure 5
  • figure 7
Highly Cited
2004
Highly Cited
2004
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.
Multiple system atrophy (MSA) has varying clinical (MSA-P versus MSA-C) and pathological [striatonigral degeneration (SND) versus… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Highly Cited
2002
Highly Cited
2002
Geographical patterns in range extension of Ponto-Caspian macroinvertebrate species in Europe
Range extensions of aquatic Ponto-Caspian macroinvertebrate species in Europe have mainly been facilitated by the interconnection… Expand
  • table 1
  • figure 1
  • table 2
  • table 3
  • figure 2
Review
2001
Review
2001
Multiple system atrophy
  • H. U. Rehman
  • Postgraduate medical journal
  • 2001
    • Corpus ID: 2749732
Multiple system atrophy (MSA) is a degenerative disease of the central nervous system. Dejerine and Thomas in 1900 were the first… Expand
Review
1997
Review
1997
Multiple system atrophy: A review of 203 pathologically proven cases
We report the clinicopathological features of 203 cases of pathologically proven multiple system atrophy (MSA) from 108… Expand
Highly Cited
1989
Highly Cited
1989
Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)
Glial cytoplasmic inclusions (GCIs) were demonstrated by silver staining, immunocytochemistry and by electron microscopy in the… Expand
Highly Cited
1989
Highly Cited
1989
Leviathan and the air-pump. Hobbes, Boyle, and the experimental life
STEVEN SHAPIN and SIMON SCHAFFER, Leviathan and the air-pump. Hobbes, Boyle, and the experimental life. Including a translation… Expand
Highly Cited
1986
Highly Cited
1986
Chronic behavioral disorders of human REM sleep: a new category of parasomnia.
Four men, aged 67-72 years, had 4-month to 6-year histories of injuring themselves or their spouses with aggressive behaviors… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • table 2
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE