Skip to search formSkip to main contentSkip to account menu

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… 
National Institutes of Health

Related topics

Related topics

25 relations
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIAATAXIA-OCULOMOTOR APRAXIA 3ATAXIA-OCULOMOTOR APRAXIA 4ATAXIA-TELANGIECTASIA-LIKE DISORDER 1

Narrower (1)

Apraxia, oculomotor, Cogan type

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
XRCC1 Mutation is Associated with PARP1 Hyperactivation and Cerebellar Ataxia
XRCC1 is a molecular scaffold protein that assembles multi-protein complexes involved in DNA single-strand break repair. Here we… 
Review
2013
Review
2013
Joubert syndrome: congenital cerebellar ataxia with the molar tooth
Highly Cited
2003
Highly Cited
2003
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor… 
Highly Cited
2002
Highly Cited
2002
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
Nephronophthisis, the most common genetic cause of chronic renal failure in children, is a progressive tubulo-interstitial kidney… 
Highly Cited
2001
Highly Cited
2001
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative disease among Europeans and people of European… 
Review
1999
Review
1999
Chronic cortical visual impairment in children: aetiology, prognosis, and associated neurological deficits
BACKGROUND/AIMS To evaluate prevalence, aetiology, prognosis, and associated neurological and ophthalmological problems in… 
Highly Cited
1992
Highly Cited
1992
Ataxia telangiectasia in the British Isles: the clinical and laboratory features of 70 affected individuals.
Seventy individuals with ataxia telangiectasia were studied: 29 females and 41 males with an age range of 2 to 42 years. The… 
Highly Cited
1988
Highly Cited
1988
Ataxia—ocular motor aprilaxia: A syndrome mimicking ataxia‐telangiectasia
We report 14 patients with a slowly progressive syndrome featuring ataxia, choreoathetosis, and ocular motor Aprilaxia in both… 
Highly Cited
1965
Highly Cited
1965
OPHTHALMIC MANIFESTATIONS OF BILATERAL NON-OCCIPITAL CEREBRAL LESIONS*
  • D. Cogan
  • The British journal of ophthalmology
  • 1965
  • Corpus ID: 37757665
To give the Montgomery Lecture is a great honour for any American but perhaps most especially appreciated by one from Boston. It… 
Highly Cited
1952
Highly Cited
1952
A type of congenital ocular motor apraxia presenting jerky head movements.
  • D. Cogan
  • Transactions - American Academy of Ophthalmology…
  • 1952
  • Corpus ID: 836358
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