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Choreoathetosis
Known as:
Choreathetosis
Â
Abnormal movement characterized by involuntary jerking and writhing affecting the limbs, trunk, and facial muscles.
National Institutes of Health
Topic mentions per year
Topic mentions per year
1949-2018
0
20
40
1949
2017
Related topics
Related topics
34 relations
2,4-Dienoyl-CoA Reductase Deficiency
ALTERNATING HEMIPLEGIA OF CHILDHOOD 1
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
Ataxia Telangiectasia
(More)
Broader (3)
Abnormal involuntary movement
Extrapyramidal Disorders
nervous system disorder
Narrower (1)
Athetosis
Related mentions per year
Related mentions per year
1936-2018
1940
1960
1980
2000
2020
Choreoathetosis
nervous system disorder
Ataxia Telangiectasia
Chorea
Dentatorubral-Pallidoluysian Atrophy
Blepharospasm
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Bilateral pallidal deep brain stimulation for the treatment of patients with dystonia-choreoathetosis cerebral palsy: a prospective pilot study.
Marie Vidailhet
,
Jérôme Yelnik
,
+29 authors
Pierre Pollak
The Lancet. Neurology
2009
BACKGROUND Cerebral palsy (CP) with dystonia-choreoathetosis is a common cause of disability in children and in adults, and…Â
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2004
2004
Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.
Shirley R Rainier
,
Donald W. Thomas
,
+9 authors
John K. Fink
Archives of neurology
2004
BACKGROUND Paroxysmal dystonic choreoathetosis (PDC) is characterized by attacks of involuntary movements that occur…Â
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Highly Cited
2002
Highly Cited
2002
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.
Heiko Krude
,
Barbara Schuetz
,
+12 authors
Annette Grueters
The Journal of clinical investigation
2002
The occurrence of neurological symptoms and developmental delay in patients affected by congenital hypothyroidism (CH) has been…Â
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Highly Cited
1994
Highly Cited
1994
Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)
Ryoji Koide
,
Toshihiko Ikeuchi
,
+13 authors
Shoji Tsuji
Nature Genetics
1994
Hereditary dentatorubral–pallidoluysian atrophy (DRPLA) is an autosomal dominant neurologic disorder characterized by variable…Â
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1985
1985
[Familial paroxysmal choreoathetosis treated with carbamazepine].
J de la Flor Bru
,
J Artigas Palláres
,
J Argemi Fontanet
,
S Salas Guzmán
Anales espanoles de pediatria
1985
Authors report a case of familial paroxysmal choreoathetosis produced by movement which improved to very-low doses of…Â
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1984
1984
Paroxysmal kinesigenic choreoathetosis
Shaul Harel
,
Uri Yurgenson
,
Miriam Kutai
Child's Nervous System
1984
A healthy intelligent 13.5-year-old boy is reported who presented with paroxysmal kinesigenic choreoathetosis. He had had…Â
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1982
1982
Nonketotic hyperglycemia appearing as choreoathetosis or ballism.
William Rector
,
H. Franklin Herlong
,
Harold L. Moses
Archives of internal medicine
1982
A number of focal neurologic abnormalities may accompany severe, nonketotic hyperglycemia, but extrapyramidal movement disorders…Â
(More)
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1980
1980
Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis.
R. L. Leibel
,
Victor Shih
,
+5 authors
C. Costello
Neurology
1980
A boy with glutaric acidemia had psychomotor retardation first noted at age 6 months, recurrent metabolic acidosis, and a…Â
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1977
1977
Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes.
James W Lance
Annals of neurology
1977
Four generations of a family are described in which 7 of 8 affected members suffered from prolonged dystonic seizures; the eighth…Â
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Highly Cited
1967
Highly Cited
1967
Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis.
Jesse Seegmiller
,
F M Rosenbloom
,
William N. Kelley
Science
1967
A sex-linked familial neurological disease consisting of cerebral palsy, mental retardation, choreoathetosis, and compulsive…Â
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