Literature DB >> 883778

Familial nonprogressive involuntary movements of childhood.

H Damasio, L Antunes, A R Damasio.   

Abstract

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Mesh：

Year:  1977        PMID： 883778     DOI： 10.1002/ana.410010619

Source DB:  PubMed          Journal:  Ann Neurol        ISSN： 0364-5134            Impact factor:   10.422


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  4 in total

1.  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

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

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

Review 3.  Benign Hereditary Chorea: An Update.

Authors:  Kathryn J Peall; Manju A Kurian
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2015-07-14

4.  SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder - deafness syndrome.

Authors:  Reem A Alkhater; Saija Ahonen; Berge A Minassian
Journal:  Ann Clin Transl Neurol       Date:  2020-11-24       Impact factor: 4.511
  4 in total

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