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Page 1
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.
Riccetto L, Vieira TP, Viguetti-Campos NL, Mazzola TN, Guaragna MS, Fabbri-Scallet H, Mello MP, Marques-de-Faria AP, Maciel-Guerra AT, Guerra Junior G. Riccetto L, et al. Among authors: mello mp. Sao Paulo Med J. 2022 Nov 28;141(4):e2022281. doi: 10.1590/1516-3180.2022.0281.R1.30082022. eCollection 2022. Sao Paulo Med J. 2022. PMID: 36449967 Free PMC article.
[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
Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in Brazil.
Belgini DR, Mello MP, Baptista MT, Oliveira DM, Denardi FC, Garmes HM, Grassiotto Oda R, Benetti Pinto CL, Marques-de-Faria AP, Maciel-Guerra AT, Guerra-Júnior G. Belgini DR, et al. Among authors: mello mp. Arq Bras Endocrinol Metabol. 2010 Nov;54(8):711-6. doi: 10.1590/s0004-27302010000800008. Arq Bras Endocrinol Metabol. 2010. PMID: 21340157
148 results