R. S. Araújo

Microconversion between CYP21A2 and CYP21A1P promoter regions causes the nonclassical form of 21-hydroxylase deficiency.

B. Mendonca, A. Barbosa, A. Billerbeck, 2007, The Journal of clinical endocrinology and metabolism.

Substitutions in the CYP21A2 promoter explain the simple‐virilizing form of 21‐hydroxylase deficiency in patients harbouring a P30L mutation

B. Mendonca, A. Billerbeck, G. Madureira, 2005, Clinical endocrinology.

Hypomagnesemia and its relation with chronic low-grade inflammation in obesity.

Kyria Jayanne Clímaco Cruz, J. B. Morais, J. S. Severo, 2017, Revista da Associacao Medica Brasileira.

[Bezafibrate in an infant with congenital generalized lipodystrophy and severe hypertriglyceridemia].

Rogério Santiago Araújo, Andressa D. Ramos, Máriton de Araújo Sousa Borges, 2013, Arquivos brasileiros de endocrinologia e metabologia.