Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Roberta Piccin de Oliveira"'
Autor:
Vera Maria Dantas, Cassandra Teixeira Valle, Roberta Piccin de Oliveira, Mylena Taíse Azevedo L. Bezerra, Cleia Teixeira do Amaral, Raissa Anielle S. Brandão, Jussara M. Cerqueira Maia, Tirzah Braz Petta
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Familial hemophagocytic lymphohistiocytosis (FHL) is a rare, potentially fatal autosomal-recessive immunodeficiency, and STXBP2 mutations have been associated with FHL type 5 (FHL-5). Here, we report a case of a 2-year-old boy who presented with recu
Externí odkaz:
https://doaj.org/article/bb7ea2be0fa54b0d9d9adb0809545805
Autor:
Raissa Anielle Silva Brandão, Tirzah Braz Petta, Mylena Bezerra, Roberta Piccin de Oliveira, Cassandra Teixeira Valle, Jussara Maia, Vera Maria Dantas, Cleia Teixeira do Amaral
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics
Frontiers in Pediatrics
Familial hemophagocytic lymphohistiocytosis (FHL) is a rare, potentially fatal autosomal-recessive immunodeficiency, and STXBP2 mutations have been associated with FHL type 5 (FHL-5). Here, we report a case of a 2-year-old boy who presented with recu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f54220ad23cbfa784ac7723e0926aa2