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Reviews in Endocrine & Metabolic Disorders|February 7, 2024
Subclinical central hypothyroidism in patients with hypothalamic-pituitary disease: does it exist?Julio Abucham, Manoel MartinsArquivos Brasileiros De Endocrinologia E Metabologia|July 23, 2011
Clomiphene fails to revert hypogonadism in most male patients with conventionally treated nonfunctioning pituitary adenomasRogerio Silicani Ribeiro, Julio AbuchamArquivos Brasileiros De Endocrinologia E Metabologia|January 31, 2006
[Glycoprotein-secreting pituitary adenomas: pathogenesis, diagnosis and treatment]Julio Abucham, Teresa C VieiraEuropean Journal of Endocrinology|April 11, 2009
Recovery of persistent hypogonadism by clomiphene in males with prolactinomas under dopamine agonist treatmentRogerio Silicani Ribeiro, Julio AbuchamArquivos Brasileiros De Endocrinologia E Metabologia|March 18, 2008
[Kallmann syndrome: a historical [corrected] clinical and molecular review]Rogério Silicani Ribeiro, Julio AbuchamArquivos Brasileiros De Endocrinologia E Metabologia|September 18, 2008
[hGH treatment impact on adrenal and thyroid functions]Manoel R A Martins, Julio AbuchamEuropean Journal of Endocrinology|March 16, 2017
MANAGEMENT OF ENDOCRINE DISEASE: Acromegaly and pregnancy: a contemporary reviewJulio Abucham, Marcello D Bronstein, Monike L DiasEuropean Journal of Endocrinology|February 27, 2007
Reversible Kallmann syndrome: report of the first case with a KAL1 mutation and literature reviewRogerio Silicani Ribeiro, Teresa Cristina Vieira, Julio AbuchamNeuroendocrinology|August 31, 2010
Short- and long-term efficacy of combined cabergoline and octreotide treatment in controlling igf-I levels in acromegalyPriscilla Mattar, Manoel Ricardo Alves Martins, Julio AbuchamArquivos Brasileiros De Endocrinologia E Metabologia|December 25, 2007
Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiencyTeresa C Vieira, Valter T Boldarine, Julio AbuchamPageof 4