Gil Guerra Jr.

A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism

A. Maciel-Guerra, M. Ribeiro, C. Hackel, 1999 .

A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency

M. de Castro, C. Longui, C. Kochi, 2016, Hormone Research in Paediatrics.

Turner's Syndrome and Thyroid Disease: A Transverse Study of Pediatric Patients in Brazil

A. Maciel-Guerra, M. Baptista, C. Medeiros, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

True Hermaphrodites in the Southeastern Region of Brazil: A Different Cytogenetic and Gonadal Profile

A. Maciel-Guerra, A. Morcillo, A. Marques-de-Faria, 1998, Journal of Pediatric Endocrinology & Metabolism (JPEM).

Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patients

A. Maciel-Guerra, S. Lemos-Marini, A. Morcillo, 2002, Journal of Bone and Mineral Metabolism.

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density

M. de Mello, A. Maciel-Guerra, S. H. V. de Lemos-Marini, 2003, Journal of Bone and Mineral Metabolism.