Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Belizário, Mirella Viviani Amaral Assis"'
Autor:
Belizário, Mirella Viviani Amaral Assis, Berlanga, Juliana Ferreira Ura, Souza, Cláudia Elaine Cestari, Moreira, Cláudia Maria Dias, Arruda, Marillis Mesquita Gonçalves de, Oliveira, Nathália de, Oliveira, Maria Inês Vaz de
Publikováno v:
Research, Society and Development; Vol. 11 No. 4; e33811427297
Research, Society and Development; Vol. 11 Núm. 4; e33811427297
Research, Society and Development; v. 11 n. 4; e33811427297
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 11 Núm. 4; e33811427297
Research, Society and Development; v. 11 n. 4; e33811427297
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Type 1 spinal muscular atrophy is a neurodegenerative disease, caused by a deletion or mutation of the SMN1 gene. There is currently only one drug approved for its treatment in Brazil, which is nusinersen. The present study aimed to carry out a liter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::d16e3e0df7916f5b4ccef4f139e0a62c
https://rsdjournal.org/index.php/rsd/article/view/27297
https://rsdjournal.org/index.php/rsd/article/view/27297
Autor:
Arruda, Marillis Mesquita Gonçalves, Berlanga , Juliana Ferreira Ura, Souza , Sandra Coenga de, Bragato , Simone Galli Rocha, Oliveira , Nathália de, Belizário , Mirella Viviani Amaral Assis, Oliveira , Maria Inez Vaz de
Publikováno v:
Research, Society and Development; Vol. 11 No. 4; e9611427075
Research, Society and Development; Vol. 11 Núm. 4; e9611427075
Research, Society and Development; v. 11 n. 4; e9611427075
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 11 Núm. 4; e9611427075
Research, Society and Development; v. 11 n. 4; e9611427075
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Spinal muscular atrophy (SMA) is a genetically-caused muscular hypotonia that can be screened through neonatal screening. Screening for the disease became recommended in 2019 by the American Panel on Traceable Diseases in Childhood, for this reason t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::5e7b45ed768d53eb5568dc31101ca044
https://rsdjournal.org/index.php/rsd/article/view/27075
https://rsdjournal.org/index.php/rsd/article/view/27075