Browsing by Author Ferraz, Lúcio Fábio Caldas
Showing results 1 to 5 of 5
Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 1-Nov-2008 | Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene | Coeli, Fernanda Borchers; Ferraz, Lúcio Fábio Caldas; Lemos-Marini, Sofia H. V. de; Rigatto, Sumara Zuanazi Pinto; Belangero, Vera Maria Santoro; de-Mello, Maricilda Palandi | - | Artigo de periódico |
| 1-Nov-2012 | 46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene | Guaragna-Filho, Guilherme; Castro, Carla Cristina Telles de Sousa; De Carvalho, Rodrigo Ribeiro; Coeli, Fernanda Borchers; Ferraz, Lúcio Fábio Caldas; Petroli, Reginaldo José; De Mello, Maricilda Palandi; Sewaybricker, Letícia Esposito; Lemos-Marini, Sofia Helena Valente; D'Souza-Li, Lilia Freire Rodrigues; Miranda, Márcio Lopes; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil | - | Artigo de periódico |
| 2005 | [5alpha-reductase Type 2 Deficiency: Experiences From Campinas (sp) And Salvador (ba)]. | Hackel, Christine; Oliveira, Luiz Eduardo C de; Toralles, Maria Betania; Nunes-Silva, Daniela; Tonini, Maria Manuela O; Ferraz, Lúcio Fábio Caldas; Steinmetz, Leandra; Damiani, Durval; Oliveira, Laurione Cândido de; Maciel-Guerra, Andréa T; Stuchi-Perez, Eliana Gabas; Guerra-Júnior, Gil | - | Artigo de periódico |
| 2012 | 46,xx Dsd And Antley-bixler Syndrome Due To Novel Mutations In The Cytochrome P450 Oxidoreductase Gene. | Guaragna-Filho, Guilherme; Castro, Carla Cristina Telles de Sousa; Carvalho, Rodrigo Ribeiro De; Coeli, Fernanda Borchers; Ferraz, Lúcio Fábio Caldas; Petroli, Reginaldo José; Mello, Maricilda Palandi De; Sewaybricker, Letícia Esposito; Lemos-Marini, Sofia Helena Valente; D'Souza-Li, Lilia Freire Rodrigues; Miranda, Márcio Lopes; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil | - | Artigo de periódico |
| 2008 | Apparent Mineralocorticoid Excess Syndrome In A Brazilian Boy Caused By The Homozygous Missense Mutation P.r186c In The Hsd11b2 Gene. | Coeli, Fernanda Borchers; Ferraz, Lúcio Fábio Caldas; Lemos-Marini, Sofia H V de; Rigatto, Sumara Zuanazi Pinto; Belangero, Vera Maria Santoro; de-Mello, Maricilda Palandi | - | Artigo de periódico |