Browsing by Author De Mello, MP

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Showing results 1 to 10 of 10
PreviewIssue DateTitleAuthor(s)AdvisorType
2013The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasiaKaupert, LC; Lemos-Marini, SHV; De Mello, MP; Moreira, RP; Brito, VN; Jorge, AAL; Longui, CA; Guerra, G; Mendonca, BB; Bachega, TA-Artigo de periódico
2002Iron-regulated proteins in Phanerochaete chrysosporium and Lentinula edodes: Differential analysis by sodium dodecyl sulfate polyacrylamide gel electrophoresis and two-dimensional polyacrylamide gel electrophoresis profilesHernandez-Macedo, ML; Ferraz, A; Rodriguez, J; Ottoboni, LMM; De Mello, MP-Artigo de periódico
1999Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiencyPaulino, LC; Araujo, M; Guerra, G; Marini, SHVL; De Mello, MP-Artigo de periódico
2011OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequencesBarros, BA; Moraes, SG; Coeli, FB; Assumpcao, JG; De Mello, MP; Maciel-Guerra, AT; Carvalho, AB; Viguetti-Campos, N; Vieira, TAP; Amstalden, EMI; Andrade, JGR; Esquiaveto-Aun, AM; Marques-de-Faria, AP; D'Souza-Li, LFR; Lemos-Marini, SHV; Guerra, G-Artigo de periódico
2001H28+C insertion in the CYP21 gene: A novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiencyLau, IF; Soardi, FC; Lemos-Marini, SHV; Guerra, G; Baptista, MTM; De Mello, MP-Artigo de periódico
2006Association between the MTHFR A1298C polymorphism and increased risk of acute myeloid leukemia in Brazilian childrenRamos, FJD; De Mello, MP; Yunes, JA; Marques-Salles, TD; Santos, N; Brandalise, SR; Pombo-de-Oliveira, MS-Artigo de periódico
2012Clinical and molecular spectrum of patients with 17 beta-hydroxysteroid dehydrogenase type 3 (17-beta-HSD3) deficiencyCastro, CCTD; Guaragna, G; Calais, FL; Coeli, FB; Leal, IRL; Cavalcante, EF; Monlleo, IL; Pereira, SRF; Silva, RBDE; Gabiatti, JRE; Marques-de-Faria, AP; Maciel-Guerra, AT; De Mello, MP; Guerra, G-Artigo de periódico
200821-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiencyTonetto-Fernandes, V; Lemos-Marini, SHV; De Mello, MP; Ribeiro, LM; Kater, CE-Artigo de periódico
2013Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuriaGuaragna, MS; Lutaif, ACGB; Piveta, CSC; Belangero, VMS; Maciel-Guerra, AT; Guerra, G; De Mello, MP-Artigo de periódico
2004Clinical findings in four Brazilian families affected by Saethre-Chotzen syndrome without TWIST mutationsNascimento, SRD; De Mello, MP; Batista, JC; Balarin, MAS; Da Silva Lopes, VLG-Artigo de periódico