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Results 21-30 of 44 (Search time: 0.05 seconds).
Issue DateTitleAuthor(s)
2020The molecular landscape of osteogenesis imperfecta in a Brazilian tertiary service cohortFERNANDES, A. M.; ROCHA-BRAZ, M. G. M.; FRANCA, M. M.; LERARIO, A. M.; SIMOES, V. R. F.; ZANARDO, E. A.; KULIKOWSKI, L. D.; MARTIN, R. M.; MENDONCA, B. B.; FERRAZ-DE-SOUZA, B.
2016Determination of nighttime salivary cortisol during pregnancy: comparison with values in non-pregnancy and Cushing's diseaseLOPES, Ludmilla Malveira Lima; FRANCISCO, Rossana Pulcineli Vieira; GALLETTA, Marco Aurelio Knippel; BRONSTEIN, Marcello Delano
2016Nutritional Aspects of Noonan Syndrome and Noonan-Related DisordersSILVA, Fernanda Marchetto da; JORGE, Alexander Augusto; MALAQUIAS, Alexandra; PEREIRA, Alexandre da Costa; YAMAMOTO, Guilherme Lopes; KIM, Chong Ae; BERTOLA, Debora
2016SAGIT (R): clinician-reported outcome instrument for managing acromegaly in clinical practice-development and results from a pilot studyGIUSTINA, Andrea; BEVAN, John S.; BRONSTEIN, Marcello D.; CASANUEVA, Felipe F.; CHANSON, Philippe; PETERSENN, Stephan; THANH, Xuan-Mai Truong; SERT, Caroline; HOUCHARD, Aude; GUILLEMIN, Isabelle; MELMED, Shlomo
2014Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian CohortPASQUALIN, Livia M. A.; REED, Umbertina C.; COSTA, Thais V. M. M.; QUEDAS, Elisangela; ALBUQUERQUE, Marco A. V.; RESENDE, Maria B. D.; RUTKOWSKI, Anne; CHADI, Gerson; ZANOTELI, Edmar
2014Prolactinomas, cabergoline, and pregnancyGLEZER, Andrea; BRONSTEIN, Marcello D.
2015Influence of growth hormone receptor (GHR) exon 3 and-202A/C IGFBP-3 genetic polymorphisms on clinical and biochemical features and therapeutic outcome of patients with acromegalyJALLAD, Raquel S.; TRARBACH, Ericka B.; DUARTE, Felipe H.; JORGE, Alexander A. L.; BRONSTEIN, Marcello D.
2021Pituitary Neoplasm Nomenclature Workshop: Does Adenoma Stand the Test of Time?HO, Ken; FLESERIU, Maria; KAISER, Ursula; SALVATORI, Roberto; BRUE, Thierry; LOPES, M. Beatriz; KUNZ, Pamela; MOLITCH, Mark; CAMPER, Sally A.; GADELHA, Monica; V, Luis Syro; LAWS, Edward; REINCKE, Martin; NISHIOKA, Hiroshi; GROSSMAN, Ashley; BARKAN, Ariel; CASANUEVA, Felipe; WASS, John; MAMELAK, Adam; KATZNELSON, Laurence; LELY, Aart J. van der; RADOVICK, Sally; BIDLINGMAIER, Martin; BOGUSZEWSKI, Margaret; BOLLERSLEV, Jens; HOFFMAN, Andrew R.; OYESIKU, Nelson; RAVEROT, Gerald; BEN-SHLOMO, Anat; FOWKES, Rob; SHIMON, Ilan; FUKUOKA, Hidenori; PEREIRA, Alberto M.; GREENMAN, Yona; HEANEY, Anthony P.; GURNELL, Mark; JOHANNSSON, Gudmundur; OSAMURA, Robert Y.; BUCHFELDER, Michael; ZATELLI, Maria Chiara; KORBONITS, Marta; CHANSON, Philippe; BIERMASZ, Nienke; CLEMMONS, David R.; KARAVITAKI, Niki; BRONSTEIN, Marcello D.; TRAINER, Peter; MELMED, Shlomo
2020Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in BrazilBERTOLA, Debora R.; CASTRO, Matheus A. A.; YAMAMOTO, Guilherme L.; HONJO, Rachel S.; CERONI, Jose Ricardo; BUSCARILLI, Michele M.; FREITAS, Amanda B.; MALAQUIAS, Alexsandra C.; PEREIRA, Alexandre C.; JORGE, Alexander A. L.; PASSOS-BUENO, Maria Rita; KIM, Chong A.
2022Clinical and genetic characterization and long-term evaluation of individuals with maturity-onset diabetes of the young (MODY): The journey towards appropriate treatmentFRANCO, Pedro Campos; SANTANA, Lucas Santos de; COSTA-RIQUETTO, Aline Dantas; SANTOMAURO JUNIOR, Augusto Cezar; JORGE, Alexander A. L.; TELES, Milena Gurgel