de Omena Filho RL - Search Results

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[Profile of patients with genitourinary anomalies treated in a clinical genetics service in the Brazilian unified health system].

Gazzaneo IF, de Queiroz CM, Goes LC, Lessa VJ, de Omena Filho RL, do Nascimento DL, Petroli RJ, Zanotti SV, Monlleó IL. Gazzaneo IF, et al. Among authors: de omena filho rl. Rev Paul Pediatr. 2016 Jan-Mar;34(1):91-8. doi: 10.1016/j.rpped.2015.06.014. Epub 2015 Oct 9. Rev Paul Pediatr. 2016. PMID: 26522823 Free PMC article.

So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity.

de Omena Filho RL, Petroli RJ, Soardi FC, de Paula Michelatto D, Mazzola TN, Fabbri-Scallet H, de Mello MP, Zanotti SV, Gubert IC, Monlleo I. de Omena Filho RL, et al. Ital J Pediatr. 2022 Jun 10;48(1):89. doi: 10.1186/s13052-022-01284-9. Ital J Pediatr. 2022. PMID: 35689291 Free PMC article.

Macrothrombocytopenia as diagnosis predictor of 22q11 deletion syndrome among patients with congenital heart defects.

Trevisan P, Barbosa S, Sperotto G, Costi C, de Omena Filho RL, Silva AP, Varella-Garcia M, Fiegenbaum M, Rosa RF, Zen PR. Trevisan P, et al. Among authors: de omena filho rl. Am J Med Genet A. 2015 Jun;167(6):1406-8. doi: 10.1002/ajmg.a.36531. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25899105 No abstract available.

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