M. Matias Baptista

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.

M. de Castro, A. Latronico, B. Mendonca, 2008, The Journal of clinical endocrinology and metabolism.

Morphometry and histology of gonads from 13 children with dysgenetic male pseudohermaphroditism.

M. Palandi de Mello, G. Guerra, M. Matias Baptista, 2001, Archives of pathology & laboratory medicine.

Evaluation of the Tubular and Interstitial Functions of the Testis in 46,XY Patients with Ambiguous Genitalia

M. de Castro, C. Lukas-Croisier, C. Hackel, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Detection of Gly-196-Ser Mutation in 5α-Reductase Type II Gene in a Brazilian Patient with Female Assignment and Behavior

A. Maciel-Guerra, C. Hackel, M. Matias Baptista, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

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.