Zobrazeno 1 - 3
of 3
pro vyhledávání: '"C R, Rieder"'
Autor:
R M, Castilhos, A F D, Souza, G V, Furtado, T C, Gheno, A L, Silva, F R, Vargas, M-A F D, Lima, O, Barsottini, J L, Pedroso, C, Godeiro, D, Salarini, E T, Pereira, K, Lin, M-B, Toralles, J A M, Saute, C R, Rieder, M, Quintas, J, Sequeiros, I, Alonso, M L, Saraiva-Pereira, L B, Jardim
Publikováno v:
Clinical genetics. 86(4)
The aim of this study was to identify the relative frequency of Huntington's disease (HD) and HD-like (HDL) disorders HDL1, HDL2, spinocerebellar ataxia type 2 (SCA2), SCA17, dentatorubral-pallidoluysian degeneration (DRPLA), benign hereditary chorea
Autor:
H.-L. Zhang, M. M. Bianchin, J. A. Bragatti, C. M. Torres, G. L. Nuernberg, C. R. Rieder, W. C. LaFrance, K. Leaver, G. D. Papadonatos, E. G. Stopa, A. S. Blum
Publikováno v:
Neurology. 76:1772-1772
Publikováno v:
Arquivos de neuro-psiquiatria. 49(3)
Involvement of the nervous system in the idiopathic hypereosinophilic syndrome is a common finding, peripheral neuropathy being the most frequent neurologic manifestation, usually appearing at the onset or following the appearance of eosinophilia. We