Skip to main content
Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1997 May;62(5):542–543. doi: 10.1136/jnnp.62.5.542-a

A case of Machado-Joseph disease presenting with spastic paraparesis.

A Kaneko, Y Narabayashi, K Itokawa, Y Nakazato, T Hosokawa, S Iwasaki, R Ohno, K Hamaguchi, M Ikeda, M Nomura
PMCID: PMC486885  PMID: 9153623

Full text

PDF

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Kawaguchi Y., Okamoto T., Taniwaki M., Aizawa M., Inoue M., Katayama S., Kawakami H., Nakamura S., Nishimura M., Akiguchi I. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet. 1994 Nov;8(3):221–228. doi: 10.1038/ng1194-221. [DOI] [PubMed] [Google Scholar]
  2. Matilla T., McCall A., Subramony S. H., Zoghbi H. Y. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease. Ann Neurol. 1995 Jul;38(1):68–72. doi: 10.1002/ana.410380113. [DOI] [PubMed] [Google Scholar]
  3. Sakai T., Kawakami H. Machado-Joseph disease: A proposal of spastic paraplegic subtype. Neurology. 1996 Mar;46(3):846–847. [PubMed] [Google Scholar]
  4. Schöls L., Vieira-Saecker A. M., Schöls S., Przuntek H., Epplen J. T., Riess O. Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients. Hum Mol Genet. 1995 Jun;4(6):1001–1005. doi: 10.1093/hmg/4.6.1001. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Neurology, Neurosurgery, and Psychiatry are provided here courtesy of BMJ Publishing Group

RESOURCES