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Issue Date | Title | Author(s) |
---|---|---|
2022 | Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant | LABELLO, Julia Haddad; BENEDETTI, Anna Flavia Figueredo; AZEVEDO, Bruna Viscardi; JORGE, Alexander Augusto de Lima; CESCATO, Valter Angelo Sperling; ROSEMBERG, Sergio; FRASSETO, Fernando Pereira; ARNHOLD, Ivo Jorge Prado; CARVALHO, Luciani Renata Silveira de |
2022 | Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature | ANDRADE, Nathalia Liberatoscioli Menezes; FUNARI, Mariana Ferreira de Assis; MALAQUIAS, Alexsandra Christianne; COLLETT-SOLBERG, Paulo Ferrez; GOMES, Nathalia L. R. A.; SCALCO, Renata; DANTAS, Naiara Castelo Branco; REZENDE, Raissa C.; TIBURCIO, Angelica M. F. P.; SOUZA, Micheline A. R.; FREIRE, Bruna L.; V, Ana C. Krepischi; LONGUI, Carlos Alberto; LERARIO, Antonio Marcondes; ARNHOLD, Ivo J. P.; JORGE, Alexander A. L.; VASQUES, Gabriela Andrade |
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