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Results 1-10 of 25 (Search time: 0.067 seconds).
Issue DateTitleAuthor(s)
2019M&M: blending medicine and musicBRONSTEIN, Marcello D.
2019Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discoveryCORREA, Fernanda A.; NAKAGUMA, Marilena; MADEIRA, Joao L. O.; NISHI, Mirian Y.; ABRAO, Milena G.; JORGE, Alexander A. L.; CARVALHO, Luciani R.; ARNHOLD, Ivo J. P.; MENDONCA, Berenice B.
2019Brazilian multicenter study on pegvisomant treatment in acromegalyBOGUSZEWSKI, Cesar L.; HUAYLLAS, Martha Katherine P.; VILAR, Lucio; NAVES, Luciana Ansaneli; RIBEIRO-OLIVEIRA JUNIOR, Antonio; SOARES, Beatriz Santana; CZEPIELEWSKI, Mauro Antonio; ABUCHAM, Julio; CORREA-SILVA, Silvia Regina; BRONSTEIN, Marcello Delano; JALLAD, Raquel Soares; DUARTE, Felipe Gaia; MUSOLINO, Nina Rosa; KASUKI, Leandro; GADELHA, Monica Roberto
2019AE&M's first issue of the year: important news!BRONSTEIN, Marcello D.
2019Active surveillance of papillary thyroid microcarcinomas in South America: Are we ready?DANILOVIC, Debora Lucia Seguro; MARTINS, Joao Roberto M.; MAIA, Ana Luiza
2020News for a New YearBRONSTEIN, Marcello D.
2019Diagnostic performance of thyroid ultrasound in Hurthle cell carcinomasSANTANA, Nathalie Oliveira; FREITAS, Ricardo Miguel Costa; MARCOS, Vinicius Neves; CHAMMAS, Maria Cristina; CAMARGO, Rosalinda Yossie Asato; SCHMERLING, Claudia Kliemann; VANDERLEI, Felipe Augusto Brasileiro; HOFF, Ana Oliveira; MARUIL, Suemi; DANILOVIC, Debora Lucia Seguro
2017Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencingCORREA, Fernanda A.; FRANCA, Marcela M.; FANG, Qing; MA, Qianyi; BACHEGA, Tania A.; RODRIGUES, Andresa; OZEL, Bilge A.; LI, Jun Z.; MENDONCA, Berenice B.; JORGE, Alexander A. L.; CARVALHO, Luciani R.; CAMPER, Sally A.; ARNHOLD, Ivo J. P.
2018Critical analysis of molecular tests in indeterminate thyroid nodulesDANILOVIC, Debora L. S.; MARUI, Suemi
2018Controversial issues in the management of hyperprolactinemia and prolactinomas - An overview by the Neuroendocrinology Department of the Brazilian Society of Endocrinology and MetabolismVILAR, Lucio; ABUCHAM, Julio; ALBUQUERQUE, Jose Luciano; ARAUJO, Luiz Antonio; AZEVEDO, Monalisa F.; BOGUSZEWSKI, Cesar Luiz; CASULARI, Luiz Augusto; CUNHA NETO, Malebranche B. C.; CZEPIELEWSKI, Mauro A.; DUARTE, Felipe H. G.; FARIA, Manuel dos S.; GADELHA, Monica R.; GARMES, Heraldo M.; GLEZER, Andrea; GURGEL, Maria Helane; JALLAD, Raquel S.; MARTINS, Manoel; MIRANDA, Paulo A. C.; MONTENEGRO, Renan M.; MUSOLINO, Nina R. C.; NAVES, Luciana A.; RIBEIRO-OLIVEIRA JUNIOR, Antonio; SILVA, Cintia M. S.; VIECCELI, Camila; BRONSTEIN, Marcello D.