Aline P. Otto

Catch-Up Growth in Patients with Congenital or Acquired Growth Hormone Deficiency After GH Replacement: Clinical Features and Hypothalamic–Pituitary Imaging

B. Mendonca, C. Leite, L. Lucato, 2012 .

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies

A. Latronico, L. Montenegro, B. Mendonca, 2015, Endocrine connections.

A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).

L. Montenegro, B. Mendonca, I. Arnhold, 2016, European journal of endocrinology.

Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center

B. Mendonca, I. Arnhold, C. Leite, 2015, Pituitary.

Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies

E. Baracat, B. Mendonca, V. Brito, 2017, Journal of the Endocrine Society.

Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort.

B. Mendonca, I. Arnhold, A. Jorge, 2014, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations

A. Jorge, B. Mendonca, M. Nishi, 2017, Clinical endocrinology.

Relatively high frequency of non‐synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly

B. Mendonca, A. Jorge, I. Arnhold, 2013, Clinical endocrinology.