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Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 geneMENDONCA, B. B; OSORIO, M. G. F; LATRONICO, A. C et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 3, pp 942-945, issn 0021-972XArticle

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A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious pubertyLATRONICO, A. C; ABELL, A. N; ARNHOLD, I. J. P et al.The Journal of clinical endocrinology and metabolism. 1998, Vol 83, Num 7, pp 2435-2440, issn 0021-972XArticle

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Mutations in the type II 3β-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girlsMARUI, S; CASTRO, M; LATRONICO, A. C et al.Clinical endocrinology (Oxford. Print). 2000, Vol 52, Num 1, pp 67-75, issn 0300-0664Article

A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiencyBILLERBECK, A. E. C; BACHEGA, T. A. S. S; FRAZZATTO, E. T et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 8, pp 2870-2872, issn 0021-972XArticle

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