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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

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Related topics

25 relations
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIAATAXIA-OCULOMOTOR APRAXIA 3ATAXIA-OCULOMOTOR APRAXIA 4ATAXIA-TELANGIECTASIA-LIKE DISORDER 1
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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… Expand
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Review
2013
Review
2013
Joubert syndrome: congenital cerebellar ataxia with the molar tooth
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked inheritance, the diagnostic hallmark of… Expand
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2008
2008
The natural history of Unverricht-Lundborg disease: a report of eight genetically proven cases.
We report eight cases of genetically proven ULD, with the aim of reassessing the clinical characteristics and natural history of… Expand
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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… Expand
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2002
2002
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
Nature Genet. 32, 300–305 (2002). Published online 9 September 2002; corrected 3 October 2002 (details online); doi:10.1038/ng996… Expand
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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… Expand
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2000
2000
Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis.
Congenital ocular motor apraxia type Cogan is characterized by impairment of horizontal voluntary eye movements, ocular… Expand
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1998
1998
Speech, cognition, and imaging studies in congenital ocular motor apraxia.
Detailed neurological, speech and language, psychological, and neuroimaging studies were carried out in eight children with the… Expand
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Highly Cited
1988
Highly Cited
1988
Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia.
We report 14 patients with a slowly progressive syndrome featuring ataxia, choreoathetosis, and ocular motor apraxia in both the… Expand
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1988
1988
Acquired ocular motor apraxia due to bilateral frontoparietal infarcts.
A case of acquired ocular motor apraxia in a 78-year-old man is reported. Disordered saccades and pursuit movements in the… Expand
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