Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Luciana Senra de Souza Sodré"'
Autor:
Luciana Senra de Souza Sodré, Rosália Maria Nunes Henriques Huaira, Fernando Antônio Basile Colugnati, Moises Carminatti, Luciane Senra de Souza Braga, Marcelo Paula Coutinho, Natália Maria da Silva Fernandes
Publikováno v:
Brazilian Journal of Nephrology, Vol 43, Iss 1, Pp 28-33 (2020)
ABSTRACT Introduction: Fabry disease is a chronic, progressive, and multi-system hereditary condition, related to an Xq22 mutation in X chromosome, which results in deficiency of alpha-galactosidase enzyme, hence reduced capacity of globotriaosylcera
Externí odkaz:
https://doaj.org/article/91c3d39675144273b30aacf11f82864a
Autor:
Luciana Senra de Souza Sodré, Rosália Maria Nunes Henriques Huaira, Marcus Gomes Bastos, Fernando Antônio Basile Colugnati, Marcelo Paula Coutinho, Natália Maria da Silva Fernandes
Publikováno v:
Kidney & Blood Pressure Research, Vol 42, Iss 6, Pp 1258-1265 (2017)
Background/Aims: Evaluate the prevalence of Fabry disease in men and women with kidney disease; and observe the presence and importance of the main signs and symptoms in patients with kidney disease. Methods: A cross-sectional analysis of secondary d
Externí odkaz:
https://doaj.org/article/a6ab29fc35ae4651acf00544c4fd2e22
Autor:
Luciane Senra de Souza Braga, Rosália Maria Nunes Henriques Huaira, Marcelo Paula Coutinho, Luciana Senra de Souza Sodré, Fernando Antonio Basile Colugnati, Natália Maria da Silva Fernandes, Carlos Alberto Huaira Contreras
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims Fabry disease is a chronic, progressive and multi-systemic hereditary condition, related to a Xq22 mutation in X chromosome, which results in deficiency of acid alpha-galactosidase, hence reduced capacity of globotriaosylceramide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a22e78fd23da973131e881176da642b
https://doi.org/10.1093/ndt/gfab080.0022
https://doi.org/10.1093/ndt/gfab080.0022