Pure sensory Guillain-Barré syndrome.

Por Miralles, F, Montero, J, Reñe, R, Martinez Matos, J A
Publicado em 1992

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient

Por Olivé, Montse, Shatunov, Alexey, Gonzalez, Laura, Carmona, Olga, Moreno, Dolores, Quereda, Lidia Gonzalez, Martinez-Matos, J.A., Goldfarb, Lev G., Ferrer, Isidro
Publicado em 2008