Literature DB >> 3950647

Coincidence of Wilson's disease with other movement disorders in the same family.

N P Quinn, C D Marsden.   

Abstract

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Year:  1986        PMID： 3950647      PMCID： PMC1028700          DOI： 10.1136/jnnp.49.2.221

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  1 in total

1.  Hereditary whispering dysphonia.

Authors:  N Parker
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-03       Impact factor: 10.154
  1 in total
  3 in total

1.  Middle-aged heterozygous carriers of Wilson's disease do not present with significant phenotypic deviations related to copper metabolism.

Authors:  G Gromadzka; G Chabik; T Mendel; A Wierzchowska; M Rudnicka; A Czlonkowska
Journal:  J Genet       Date:  2010-12       Impact factor: 1.166

2.  Movement disorder associated with abnormal copper metabolism and decreased blood antioxidants.

Authors:  H S Pall; A C Williams; D R Blake; P Winyard; S Chirico; S Brailsford
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-09       Impact factor: 10.154

3.  Ceruloplasmin and superoxide dismutase (SOD1) in heterozygotes for Wilson disease: A case control study.

Authors:  Gudlaug Tórsdóttir; Grétar Gudmundsson; Jakob Kristinsson; Jón Snaedal; Torkell Jóhannesson
Journal:  Neuropsychiatr Dis Treat       Date:  2009-04-08       Impact factor: 2.570
  3 in total

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