Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Fernanda M. Fonseca"'
Autor:
Rafael O. Trevisan, Jerusa M. Oliveira, Hugo F. Perini, Ulisses Travaglini, Thaís K. de L. Rezende, Francisco R.A. dos Santos, Luciana R. de S. Floresta, Ana L.S. Borges, Leticia C. Ruiz, Leonardo E. de A. e Silva, Juliane Z. Marinho, Fernanda M. Fonseca, Carlo J.F. de Oliveira, Virmondes R. Júnior, Marcos V. da Silva, Lucas Anhezini, Anielle Christine A. Silva
Publikováno v:
Next Materials, Vol 7, Iss , Pp 100447- (2025)
Nanoparticles with bactericidal properties offer significant advantages, and their integration with other nanomaterials can further enhance these benefits. This study investigates the synergistic effects of Ag-doped ZnO/AgO (ZnAg) nanocomposites comb
Externí odkaz:
https://doaj.org/article/952f6fddaf2747ff97b4e1551f8fd14e
Autor:
Kennio Ferreira-Paim, Leonardo Andrade-Silva, Fernanda M Fonseca, Thatiana B Ferreira, Delio J Mora, Juliana Andrade-Silva, Aziza Khan, Aiken Dao, Eduardo C Reis, Margarete T G Almeida, Andre Maltos, Virmondes R Junior, Luciana Trilles, Volker Rickerts, Ariya Chindamporn, Jane E Sykes, Massimo Cogliati, Kirsten Nielsen, Teun Boekhout, Matthew Fisher, June Kwon-Chung, David M Engelthaler, Marcia Lazéra, Wieland Meyer, Mario L Silva-Vergara
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 11, Iss 1, p e0005223 (2017)
Cryptococcosis is an important fungal infection in immunocompromised individuals, especially those infected with HIV. In Brazil, despite the free availability of antiretroviral therapy (ART) in the public health system, the mortality rate due to Cryp
Externí odkaz:
https://doaj.org/article/26e9412f0b634d0b8c08d7fa8841f6d2
Publikováno v:
Revista Hospital Universitário Pedro Ernesto. 15
Introducao: A deficiencia de 17alfa-hidroxilase e uma doenca autossomica recessiva, causa rara de hiperplasia adrenal congenita, por mutacao no gene CYP17A1 que codifica o citocromo P450c17. E caracterizada por infantilismo sexual, hipertensao arteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf17ce928da0aebfb12c44694688bb32
https://doi.org/10.12957/rhupe.2016.28245
https://doi.org/10.12957/rhupe.2016.28245
Autor:
Rachel Sayuri Honjo, Débora Romeo Bertola, Patrícia de Campos Pieri, Chong Ae Kim, Roberta Lelis Dutra, Fernanda Sarquis Jehee, Leslie Domenici Kulikowski, Fernanda M Fonseca
Publikováno v:
BMC Research Notes, Vol 5, Iss 1, p 13 (2012)
BMC Research Notes
BMC Research Notes
Background Williams-Beuren syndrome (WBS; OMIM 194050) is caused by a hemizygous contiguous gene microdeletion at 7q11.23. Supravalvular aortic stenosis (SVAS), mental retardation, and overfriendliness comprise typical symptoms of WBS. Although fluor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8db05897ab102a44a8a5422cab85a2e1
http://www.biomedcentral.com/1756-0500/5/13
http://www.biomedcentral.com/1756-0500/5/13