Skip to main content

. 1996 May;60(5):586–588. doi: 10.1136/jnnp.60.5.586-a

Coexistence of type I familial amyloid polyneuropathy and spinocerebellar ataxia type 1. Clinical and genetic studies of a Japanese family.

S Ikeda, N Yanagisawa, N Hanyu, K Furihata, T Kobayashi

PMCID: PMC486380 PMID: 8778271

586

Images in this article

Selected References

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

Ikeda S., Hanyu N., Hongo M., Yoshioka J., Oguchi H., Yanagisawa N., Kobayashi T., Tsukagoshi H., Ito N., Yokota T. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients. Brain. 1987 Apr;110(Pt 2):315–337. doi: 10.1093/brain/110.2.315. [DOI] [PubMed] [Google Scholar]
Nakazato M., Ikeda S., Shiomi K., Matsukura S., Yoshida K., Shimizu H., Atsumi T., Kangawa K., Matsuo H. Identification of a novel transthyretin variant (Val30----Leu) associated with familial amyloidotic polyneuropathy. FEBS Lett. 1992 Jul 20;306(2-3):206–208. doi: 10.1016/0014-5793(92)81001-3. [DOI] [PubMed] [Google Scholar]
Orr H. T., Chung M. Y., Banfi S., Kwiatkowski T. J., Jr, Servadio A., Beaudet A. L., McCall A. E., Duvick L. A., Ranum L. P., Zoghbi H. Y. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 1993 Jul;4(3):221–226. doi: 10.1038/ng0793-221. [DOI] [PubMed] [Google Scholar]
Sasaki H., Sakaki Y., Matsuo H., Goto I., Kuroiwa Y., Sahashi I., Takahashi A., Shinoda T., Isobe T., Takagi Y. Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques. Biochem Biophys Res Commun. 1984 Dec 14;125(2):636–642. doi: 10.1016/0006-291x(84)90586-2. [DOI] [PubMed] [Google Scholar]
Zoghbi H. Y., Pollack M. S., Lyons L. A., Ferrell R. E., Daiger S. P., Beaudet A. L. Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred. Ann Neurol. 1988 Jun;23(6):580–584. doi: 10.1002/ana.410230609. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES