Literature DB >> 4795418

A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism.

R Willvonseder, N P Goldstein, J T McCall, R E Yoss, W N Tauxe.   

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Year:  1973        PMID： 4795418     DOI： 10.1212/wnl.23.10.1039

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  4 in total

1.  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

Review 2.  An unusual neurological disorder with abnormal copper metabolism.

Authors:  S Ono; H Kurisaki
Journal:  J Neurol       Date:  1988-09       Impact factor: 4.849

3.  [Dermatoglyphics of homo- and heterozygotes for Wilson's disease (hepatolenticular degeneration) (author's transl)].

Authors:  W Vormittag; M Weninger; R Willvonseder; F Wewalka
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

4.  Sibling cases of a degenerative neurological disease associated with hypocupraemia and hypobetalipoproteinaemia.

Authors:  Y Iwakawa; M Shimohira; J Kohyama; H Kodama
Journal:  Eur J Pediatr       Date:  1993-04       Impact factor: 3.183
  4 in total

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