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46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene.
Guaragna-Filho G, Castro CC, Carvalho RR, Coeli FB, Ferraz LF, Petroli RJ, Mello MP, Sewaybricker LE, Lemos-Marini SH, D'Souza-Li LF, Miranda ML, Maciel-Guerra AT, Guerra-Junior G. Guaragna-Filho G, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):578-85. doi: 10.1590/s0004-27302012000800020. Arq Bras Endocrinol Metabol. 2012. PMID: 23295302
[Multicentric study of Brazilian patients with 21-hydroxylase deficiency: a genotype-phenotype correlation].
Bachega TA, Billerbeck AE, Parente EB, Lemos-Marini SH, Baptista MT, Mello MP, Guerra G Jr, Kuperman H, Setian N, Damiani D, Torres N, Castro Md, Mendonça BB. Bachega TA, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2004 Oct;48(5):697-704. doi: 10.1590/s0004-27302004000500016. Epub 2005 Mar 7. Arq Bras Endocrinol Metabol. 2004. PMID: 15761541 Review. Portuguese.
[Genes involved in sex determination and differentiation].
Mello MP, Assumpção Jde G, Hackel C. Mello MP, et al. Arq Bras Endocrinol Metabol. 2005 Feb;49(1):14-25. doi: 10.1590/s0004-27302005000100004. Epub 2006 Mar 16. Arq Bras Endocrinol Metabol. 2005. PMID: 16544031 Review. Portuguese.
[True hermaphroditism: experience with 36 patients].
Damiani D, Guedes DR, Damiani D, Setian N, Maciel-Guerra AT, Mello MP, Guerra-Júnior G. Damiani D, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2005 Feb;49(1):71-8. doi: 10.1590/s0004-27302005000100009. Epub 2006 Mar 16. Arq Bras Endocrinol Metabol. 2005. PMID: 16544036 Portuguese.
[XX male: 3 case reports during childhood].
Damiani D, Guedes DR, Damiani D, Dichtchekenian V, Coelho Neto JR, Maciel-Guerra AT, Guerra-Júnior G, Mello MP, Setian N. Damiani D, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2005 Feb;49(1):79-82. doi: 10.1590/s0004-27302005000100010. Epub 2006 Mar 16. Arq Bras Endocrinol Metabol. 2005. PMID: 16544037 Portuguese.
Absence of mutations in Pax6 gene in three cases of morning glory syndrome associated with isolated growth hormone deficiency.
Guerra-Junior G, Spinola-Castro AM, Siviero-Miachon AA, Nogueira RG, Lemos-Marini SH, D'Souza-Li LF, Silva PC, França ES, Soardi FC, Mello MP. Guerra-Junior G, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1221-7. doi: 10.1590/s0004-27302008000800004. Arq Bras Endocrinol Metabol. 2008. PMID: 19169473
Clinical and genetic findings of five patients with WT1-related disorders.
Andrade JG, Guaragna MS, Soardi FC, Guerra-Júnior G, Mello MP, Maciel-Guerra AT. Andrade JG, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1236-43. doi: 10.1590/s0004-27302008000800006. Arq Bras Endocrinol Metabol. 2008. PMID: 19169475
151 results