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Metabolites|December 23, 2022
Childhood-Onset GH Deficiency versus Adult-Onset GH Deficiency: Relevant Differences Regarding Insulin SensitivityHeraldo Mendes Garmes, Alejandro Rosell Castillo, Sarah Monte Alegre, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 9, 2018
Three new Brazilian cases of 17α-hydroxylase deficiency: clinical, molecular, hormonal, and treatment featuresIkaro Soares Santos Breder, Heraldo Mendes Garmes, Tais Nitsch Mazzola, et al.
Revista Brasileira De Ginecologia E Obstetricia : Revista Da Federacao Brasileira Das Sociedades De Ginecologia E Obstetricia|April 16, 2026
Prolactinomas treated with dopaminergic agonists: behavior in different moments of lifeMarcela Souza Carneiro, Heraldo Mendes Garmes, Gabriela Pravatta-Rezende, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|October 30, 2014
Pituitary macroadenoma presenting as a nasal tumor: case reportNivaldo Adolfo Silva Junior, Fabiano Reis, Larissa Kaori Miura, et al.
Fertility and Sterility|November 29, 2011
A pituitary adenoma secreting follicle-stimulating hormone with ovarian hyperstimulation: treatment using a gonadotropin-releasing hormone antagonistHeraldo Mendes Garmes, Oswaldo Rocha Grassiotto, Yvens Barbosa Fernandes, et al.
Surgical Neurology International|August 26, 2017
Pituitary carcinoma: A case report and discussion of potential value of combined use of Ga-68 DOTATATE and F-18 FDG PET/CT scan to better choose therapyHeraldo Mendes Garmes, José Barreto Campello Carvalheira, Fabiano Reis, et al.
The Journal of Clinical Endocrinology and Metabolism|August 3, 2006
Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmiaEricka Barbosa Trarbach, Elaine Maria Frade Costa, Beatriz Versiani, et al.
Radiologia Brasileira|December 22, 2025
Pituitary macroadenoma: less common neuroimaging features in a common lesionFernanda Veloso Pereira, Natália Yaktine Yoshida, Davi Ferreira Soares, et al.
The Journal of Clinical Endocrinology and Metabolism|August 7, 2008
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndromeAna Paula Abreu, Ericka Barbosa Trarbach, Margaret de Castro, et al.
Archives of Endocrinology and Metabolism|June 25, 2026
Catheterization of the petrosal sinus: possible advantage of desmopressin stimulation in Cushing diseaseHeraldo Mendes Garmes, Sara Calazans de Siqueira, Karla Borges Daniel, et al.
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