Found: 5
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Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons.
- Published in:
- Acta Neuropathologica, 2007, v. 113, n. 2, p. 205, doi. 10.1007/s00401-006-0151-z
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- Article
Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes.
- Published in:
- Acta Neuropathologica, 2006, v. 112, n. 3, p. 341, doi. 10.1007/s00401-006-0093-5
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- Article
Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions?: Report of an autopsy case and a review of the literature.
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- Acta Neuropathologica, 2003, v. 105, n. 6, p. 615, doi. 10.1007/s00401-003-0687-0
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- Article
Sacsin-related ataxia with neither retinal hypermyelination nor spasticity.
- Published in:
- Movement Disorders, 2007, v. 22, n. 9, p. 1362, doi. 10.1002/mds.21557
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- Article
Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 1, p. 99, doi. 10.1093/hmg/8.1.99
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- Article