Zobrazeno 1 - 10
of 75
pro vyhledávání: '"J L Pedroso"'
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 2b, Pp 288-291 (2011)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterized by late-infantile onset spastic ataxia and other neurological features. ARSACS has a high prevalence in northeastern Quebec, Canada. Seve
Externí odkaz:
https://doaj.org/article/a4537fcf1c1f479bb144cff60baad340
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 2b, Pp 406-407 (2011)
Externí odkaz:
https://doaj.org/article/2f2267e73319453aae15c2a9e9bf136e
Autor:
P Braga-Neto, J L Pedroso, A C Felício, A Abrahão, L A Dutra, M L E Bezerra, O G P Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 2b, Pp 405-406 (2011)
Externí odkaz:
https://doaj.org/article/d06138e0923b45a3890a58573e7fe414
Autor:
Silva-Rodrigues, Gislaine1 (AUTHOR) gislaine.srodrigues@uel.br, Castro, Isabela Madeira de1 (AUTHOR) isabela.mcastro@uel.br, Borges, Paulo Henrique Guilherme1 (AUTHOR) paulo.guilhermeph@uel.br, Suzukawa, Helena Tiemi1 (AUTHOR) helena.tiemi.suzukawa@uel.br, Souza, Joyce Marinho de1 (AUTHOR) lionilmy@uel.br, Bartolomeu-Gonçalves, Guilherme2 (AUTHOR), Pelisson, Marsileni2 (AUTHOR), Medeiros, Cássio Ilan Soares3 (AUTHOR) cassioism@hotmail.com, Bispo, Marcelle de Lima Ferreira4 (AUTHOR) mlfbispo@uel.br, Almeida, Ricardo Sérgio Couto de1 (AUTHOR), Ishida, Kelly5 (AUTHOR) ishidakelly@usp.br, Tavares, Eliandro Reis6,7 (AUTHOR) tavares.eliandro@gmail.com, Yamauchi, Lucy Megumi1,7 (AUTHOR), Yamada-Ogatta, Sueli Fumie1,2,7 (AUTHOR) ogatta@uel.br
Publikováno v:
Pharmaceutics. Aug2024, Vol. 16 Issue 8, p1053. 25p.
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:
Toala Soledispa, Raúl Alexander1, Pedroso Sosa, Rodolfo2, Burgos Macías, Daniel Isaías2, Roller Gutiérrez, Felicia2
Publikováno v:
La Técnica: Revista de las Agrociencias. jan-jun2024, Vol. 14 Issue 1, p1-11. 11p.
Autor:
Pinto, Paula Campos1 (AUTHOR) mppinto@edu.ulisboa.pt, Fontes, Fernando2 (AUTHOR), Neca, Patrícia3 (AUTHOR), Bento, Sofia3 (AUTHOR), Alves, Joana Pimentel2 (AUTHOR)
Publikováno v:
Journal of Applied Research in Intellectual Disabilities. Sep2023, Vol. 36 Issue 5, p1092-1100. 9p.
Autor:
Silva Vasconcelos, Priscilla Guimarães, Kyu Min Lee, Flores Abuna, Gabriel, Melo Brito Costa, Edja Maria, Mendonça Murata, Ramiro
Publikováno v:
Frontiers in Pharmacology; 2024, p1-11, 11p
Autor:
Zaib, Sumera1 (AUTHOR) sumera.zaib@ucp.edu.pk, Javed, Hira1 (AUTHOR), Khan, Imtiaz2 (AUTHOR) kimtiaz@hotmail.co.uk, Jaber, Fadi3,4 (AUTHOR), Sohail, Ali1 (AUTHOR), Zaib, Zainab5 (AUTHOR), Mehboob, Tooba6 (AUTHOR), Tabassam, Naila6 (AUTHOR), Ogaly, Hanan A.7 (AUTHOR)
Publikováno v:
ChemistrySelect. 5/25/2023, Vol. 8 Issue 20, p1-19. 19p.
Publikováno v:
Neurology; 3/12/2024, Vol. 102 Issue 5, p1-2, 2p