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Issue Date | Title | Author(s) |
---|---|---|
2016 | The Frequency of Pathogenic Copy Number Variants in Children with Short Stature of Unknown Etiology | CANTON, A.; HOMMA, T.; FURUYA, T.; ROELA, R.; ARNHOLD, I; JORGE, A. |
2016 | Estado Mixedematoso | DANILOVIC, Debora Lucia Seguro; ALMEIDA, Madson Queiroz de; MARTINS, Herlon Saraiva; BRANDãO NETO, Rodrigo Antonio |
2016 | Crise Tireotóxica | DANILOVIC, Debora Lucia Seguro; ALMEIDA, Madson Queiroz de; MARTINS, Herlon Saraiva; BRANDãO NETO, Rodrigo Antonio |
2016 | Growth Hormone (GH) Deficiency Type II: Clinical and Molecular Evidence of Impaired Regulated GH Secretion Due to an Gln181Arg GH-1 Gene Mutation | MILETTA, Maria Consolata; EBLE, Andree; ARNHOLD, Ivo J. P.; DAUBER, Andrew; FLUCK, Christa; PANDEY, Amit |
2016 | Hipopituitarismo | CARVALHO, Luciani Renata Silveira de; JALLAD, Raquel Soares; ARNHOLD, Ivo Jorge Prado |
2016 | Hiperparatireoidismo Primário | MARTIN, Regina Matsunaga; SOUZA, Bruno Ferraz de; CORRêA, Pedro Henrique Silveira |
2016 | Hipercalcemia Independente de PTH | SOUZA, Bruno Ferraz de; MARTIN, Regina Matsunaga |
2016 | Displasia Fibrosa | MACHADO, Luana Gerheim; MARTIN, Regina Matsunaga |
2016 | A META-ANALYSIS OF THE ROLE OF ADJUVANT RADIOTHERAPY AFTER SURGERY FOR ADRENOCORTICAL CARCINOMA | SROUGI, Victor; BESSA, Jose; TANNO, Fabio; FERREIRA, Amanda; LOUSADA, Lia; ALMEIDA, Madson; ALMEDA, Cristiane; SROUGI, Miguel; MENDONCA, Berenice; HOFF, Ana; CHAMBO, Jose; FRAGOSO, Maria |
2016 | Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case | STECCHINI, M.; MACEDO, D.; REIS, A. C.; ABREU, A. P.; MOREIRA, A.; CASTRO, M.; KAISER, U.; LATRONICO, A. C.; ANTONINI, S. |