| Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 2013 | The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia | Kaupert, LC; Lemos-Marini, SHV; De Mello, MP; Moreira, RP; Brito, VN; Jorge, AAL; Longui, CA; Guerra, G; Mendonca, BB; Bachega, TA | - | Artigo de periódico |
| 2002 | Iron-regulated proteins in Phanerochaete chrysosporium and Lentinula edodes: Differential analysis by sodium dodecyl sulfate polyacrylamide gel electrophoresis and two-dimensional polyacrylamide gel electrophoresis profiles | Hernandez-Macedo, ML; Ferraz, A; Rodriguez, J; Ottoboni, LMM; De Mello, MP | - | Artigo de periódico |
| 1999 | Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency | Paulino, LC; Araujo, M; Guerra, G; Marini, SHVL; De Mello, MP | - | Artigo de periódico |
| 2011 | OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences | Barros, 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 |
| 2001 | H28+C insertion in the CYP21 gene: A novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency | Lau, IF; Soardi, FC; Lemos-Marini, SHV; Guerra, G; Baptista, MTM; De Mello, MP | - | Artigo de periódico |
| 2006 | Association between the MTHFR A1298C polymorphism and increased risk of acute myeloid leukemia in Brazilian children | Ramos, FJD; De Mello, MP; Yunes, JA; Marques-Salles, TD; Santos, N; Brandalise, SR; Pombo-de-Oliveira, MS | - | Artigo de periódico |
| 2012 | Clinical and molecular spectrum of patients with 17 beta-hydroxysteroid dehydrogenase type 3 (17-beta-HSD3) deficiency | Castro, 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 |
| 2008 | 21-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiency | Tonetto-Fernandes, V; Lemos-Marini, SHV; De Mello, MP; Ribeiro, LM; Kater, CE | - | Artigo de periódico |
| 2013 | Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria | Guaragna, MS; Lutaif, ACGB; Piveta, CSC; Belangero, VMS; Maciel-Guerra, AT; Guerra, G; De Mello, MP | - | Artigo de periódico |
| 2004 | Clinical findings in four Brazilian families affected by Saethre-Chotzen syndrome without TWIST mutations | Nascimento, SRD; De Mello, MP; Batista, JC; Balarin, MAS; Da Silva Lopes, VLG | - | Artigo de periódico |
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