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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…
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National Institutes of Health
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Related topics
Related topics
25 relations
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
ATAXIA-OCULOMOTOR APRAXIA 3
ATAXIA-OCULOMOTOR APRAXIA 4
ATAXIA-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
N. Hoch
,
H. Hanzlíková
,
+14 authors
K. Caldecott
Nature
2017
Corpus ID: 4450725
XRCC1 is a molecular scaffold protein that assembles multi-protein complexes involved in DNA single-strand break repair. Here we…
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Review
2013
Review
2013
Joubert syndrome: congenital cerebellar ataxia with the molar tooth
M. Romani
,
A. Micalizzi
,
E. Valente
The Lancet Neurology
2013
Corpus ID: 19839307
Highly Cited
2003
Highly Cited
2003
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
I. Le Ber
,
M. Moreira
,
+12 authors
A. Dürr
Brain : a journal of neurology
2003
Corpus ID: 18999376
Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor…
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Highly Cited
2002
Highly Cited
2002
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
G. Mollet
,
R. Salomon
,
+8 authors
S. Saunier
Nature Genetics
2002
Corpus ID: 24216974
Nephronophthisis, the most common genetic cause of chronic renal failure in children, is a progressive tubulo-interstitial kidney…
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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
H. Date
,
O. Onodera
,
+18 authors
S. Tsuji
Nature Genetics
2001
Corpus ID: 25665707
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative disease among Europeans and people of European…
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Review
1999
Review
1999
Chronic cortical visual impairment in children: aetiology, prognosis, and associated neurological deficits
R. Huo
,
S. Burden
,
C. Hoyt
,
W. Good
The British journal of ophthalmology
1999
Corpus ID: 34684846
BACKGROUND/AIMS To evaluate prevalence, aetiology, prognosis, and associated neurological and ophthalmological problems in…
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Highly Cited
1992
Highly Cited
1992
Ataxia telangiectasia in the British Isles: the clinical and laboratory features of 70 affected individuals.
C. Woods
,
A. Taylor
The Quarterly journal of medicine
1992
Corpus ID: 43495679
Seventy individuals with ataxia telangiectasia were studied: 29 females and 41 males with an age range of 2 to 42 years. The…
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Highly Cited
1988
Highly Cited
1988
Ataxia—ocular motor aprilaxia: A syndrome mimicking ataxia‐telangiectasia
J. Aicardi
,
C. Barbosa
,
+6 authors
Paul Moe
Annals of neurology
1988
Corpus ID: 45836910
We report 14 patients with a slowly progressive syndrome featuring ataxia, choreoathetosis, and ocular motor Aprilaxia in both…
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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…
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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
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