Literature DB >> 4269386

Benign familial chorea with onset in childhood.

R W Chun, R F Daly, B J Mansheim, G J Wolcott.   

Abstract

Entities:  

Mesh：

Year:  1973        PMID： 4269386

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  7 in total

1.  Familial essential ("benign") chorea.

Authors:  T D Bird; C B Carlson; J G Hall
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

2.  Benign hereditary chorea of early onset maps to chromosome 14q.

Authors:  B B de Vries; W F Arts; G J Breedveld; J J Hoogeboom; M F Niermeijer; P Heutink
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

3.  Hereditary progressive chorea without dementia.

Authors:  W Schady; R J Meara
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-02       Impact factor: 10.154

4.  Benign (non-paroxysmal) familial chorea. Paediatric perspectives.

Authors:  G Sleigh; R H Lindenbaum
Journal:  Arch Dis Child       Date:  1981-08       Impact factor: 3.791

5.  Benign familial chorea: an association with intellectual impairment.

Authors:  D A Leli; T W Furlow; J C Falgout
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-05       Impact factor: 10.154

Review 6.  A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.

Authors:  Liana Veneziano; Michael H Parkinson; Elide Mantuano; Marina Frontali; Kailash P Bhatia; Paola Giunti
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

Review 7.  Genetic disorders of thyroid metabolism and brain development.

Authors:  Manju A Kurian; Heinz Jungbluth
Journal:  Dev Med Child Neurol       Date:  2014-03-26       Impact factor: 5.449
  7 in total

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