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

Oculomotor apraxia

Known as: Ocular Motor Apraxia, Oculomotor dyspraxia 
Ocular motor apraxia is a deficiency in voluntary, horizontal, lateral, fast eye movements (saccades) with retention of slow pursuit movements. The… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
XRCC1 is a molecular scaffold protein that assembles multi-protein complexes involved in DNA single-strand break repair. Here we… Expand
Is this relevant?
Review
2013
Review
2013
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked inheritance, the diagnostic hallmark of… Expand
Is this relevant?
2008
2008
We report eight cases of genetically proven ULD, with the aim of reassessing the clinical characteristics and natural history of… Expand
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor… Expand
  • table 1
  • figure 1
  • figure 2
  • table 2
  • figure 3
Is this relevant?
2002
2002
Nature Genet. 32, 300–305 (2002). Published online 9 September 2002; corrected 3 October 2002 (details online); doi:10.1038/ng996… Expand
  • table 1
Is this relevant?
Highly Cited
2001
Highly Cited
2001
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative disease among Europeans and people of European… Expand
  • table 1
  • figure 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?
2000
2000
Congenital ocular motor apraxia type Cogan is characterized by impairment of horizontal voluntary eye movements, ocular… Expand
Is this relevant?
1998
1998
Detailed neurological, speech and language, psychological, and neuroimaging studies were carried out in eight children with the… Expand
Is this relevant?
Highly Cited
1988
Highly Cited
1988
We report 14 patients with a slowly progressive syndrome featuring ataxia, choreoathetosis, and ocular motor apraxia in both the… Expand
Is this relevant?
1988
1988
A case of acquired ocular motor apraxia in a 78-year-old man is reported. Disordered saccades and pursuit movements in the… Expand
Is this relevant?