Dominant spino-pontine atrophy. Report of a family through three generations
- PMID: 5571046
- DOI: 10.1093/brain/94.2.349
Dominant spino-pontine atrophy. Report of a family through three generations
Similar articles
-
Spino-pontine degeneration.Eur Neurol. 1969;2(6):356-73. doi: 10.1159/000113812. Eur Neurol. 1969. PMID: 5808476 No abstract available.
-
The hereditary ataxias.Prog Med Genet. 1985;6:123-240. Prog Med Genet. 1985. PMID: 2425393 Review. No abstract available.
-
Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations.Arch Neurol. 1967 Apr;16(4):364-76. doi: 10.1001/archneur.1967.00470220028004. Arch Neurol. 1967. PMID: 6021917 No abstract available.
-
The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.Brain. 1982 Mar;105(Pt 1):1-28. doi: 10.1093/brain/105.1.1. Brain. 1982. PMID: 7066668
-
Joseph disease: an autosomal dominant motor system degeneration.Adv Neurol. 1984;41:179-93. Adv Neurol. 1984. PMID: 6388271 Review. No abstract available.
Cited by
-
Toward understanding Machado-Joseph disease.Prog Neurobiol. 2012 May;97(2):239-57. doi: 10.1016/j.pneurobio.2011.11.006. Epub 2011 Nov 23. Prog Neurobiol. 2012. PMID: 22133674 Free PMC article. Review.
-
Genetic and clinical patterns of heritable cerebellar ataxias in adults. II. Clinical manifestations.J Med Genet. 1981 Aug;18(4):276-84. doi: 10.1136/jmg.18.4.276. J Med Genet. 1981. PMID: 7277421 Free PMC article.
-
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.Acta Neuropathol. 1987;75(1):51-61. doi: 10.1007/BF00686793. Acta Neuropathol. 1987. PMID: 3481153
-
The pathology of Machado-Joseph disease. Report of a possible homozygous case.Acta Neuropathol. 1982;58(1):48-54. doi: 10.1007/BF00692697. Acta Neuropathol. 1982. PMID: 7136516
-
An unusual association of dentato-rubral degeneration with spinal ataxia, ophthalmoplegia and multiple cranial nerve palsies.J Neurol. 1985;231(6):319-23. doi: 10.1007/BF00313709. J Neurol. 1985. PMID: 3973640
MeSH terms
LinkOut - more resources
Full Text Sources