1.
Eur Neurol
; 83(1): 99-104, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32344416
RESUMO
Machado-Joseph disease (MJD), or spinocerebellar ataxia type 3, was originally described in members of the families of Machado, Thomas, and Joseph from São Miguel Island, Azores, Portugal, in 1972. The purpose of this article is to present previous descriptions of hereditary ataxia resembling the heterogeneous phenotypic intra-familiar presentation of MJD. We suggest that the condition would best be called dominant spino-pontine atrophy.
Assuntos
Doença de Machado-Joseph/história , História do Século XIX , História do Século XX , Humanos
2.
Buenos Aires; Sagitario; 1a. ed; 1997. 495 p. 23 cm. (72810).
Monografia
em Espanhol
| BINACIS
| ID: bin-72810
3.
Buenos Aires; Sagitario; 1a. ed; 1997. 495 p. 23 cm.
Monografia
em Espanhol
|
LILACS-Express
| BINACIS
| ID: biblio-1198109