M. P. de-Mello

Growth in patients with the salt-wasting form of congenital adrenal hyperplasia during the first two years of life

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2009 .

Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.

F. C. Soardi, L. D’Souza-Li, V. Belangero, 2008, Arquivos brasileiros de endocrinologia e metabologia.

Novel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency

G. Guerra‐Júnior, F. C. Soardi, R. J. Petroli, 2010, BMC Medical Genetics.

Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency.

M. P. de-Mello, G. Guerra, M. Sanches, 1996, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Normalization of height and excess body fat in children with salt-wasting 21-hydroxylase deficiency.

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2011, Jornal de pediatria.

Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.

Vera Maria Santoro Belangero, Fernanda Borchers Coeli, Lúcio Fábio Caldas Ferraz, 2008, Arquivos brasileiros de endocrinologia e metabologia.

Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiency.

D. Santos, G. Guerra‐Júnior, E. Gonçalves, 2012, Nutrition.

Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with Its Development in Congenital Adrenal Hyperplasia

G. Guerra‐Júnior, A. Morcillo, L. C. de Oliveira, 2018, Hormone Research in Paediatrics.

Normalization of height and excess body fat in children with salt-wasting 21-hydroxylase deficiency.

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2011, Jornal de pediatria.