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Results 1-10 of 83 (Search time: 0.006 seconds).
Issue DateTitleAuthor(s)
2016The Frequency of Pathogenic Copy Number Variants in Children with Short Stature of Unknown EtiologyCANTON, A.; HOMMA, T.; FURUYA, T.; ROELA, R.; ARNHOLD, I; JORGE, A.
2016Estado MixedematosoDANILOVIC, Debora Lucia Seguro; ALMEIDA, Madson Queiroz de; MARTINS, Herlon Saraiva; BRANDãO NETO, Rodrigo Antonio
2016Crise TireotóxicaDANILOVIC, Debora Lucia Seguro; ALMEIDA, Madson Queiroz de; MARTINS, Herlon Saraiva; BRANDãO NETO, Rodrigo Antonio
2016Growth Hormone (GH) Deficiency Type II: Clinical and Molecular Evidence of Impaired Regulated GH Secretion Due to an Gln181Arg GH-1 Gene MutationMILETTA, Maria Consolata; EBLE, Andree; ARNHOLD, Ivo J. P.; DAUBER, Andrew; FLUCK, Christa; PANDEY, Amit
2016HipopituitarismoCARVALHO, Luciani Renata Silveira de; JALLAD, Raquel Soares; ARNHOLD, Ivo Jorge Prado
2016Hiperparatireoidismo PrimárioMARTIN, Regina Matsunaga; SOUZA, Bruno Ferraz de; CORRêA, Pedro Henrique Silveira
2016Hipercalcemia Independente de PTHSOUZA, Bruno Ferraz de; MARTIN, Regina Matsunaga
2016Displasia FibrosaMACHADO, Luana Gerheim; MARTIN, Regina Matsunaga
2016A META-ANALYSIS OF THE ROLE OF ADJUVANT RADIOTHERAPY AFTER SURGERY FOR ADRENOCORTICAL CARCINOMASROUGI, Victor; BESSA, Jose; TANNO, Fabio; FERREIRA, Amanda; LOUSADA, Lia; ALMEIDA, Madson; ALMEDA, Cristiane; SROUGI, Miguel; MENDONCA, Berenice; HOFF, Ana; CHAMBO, Jose; FRAGOSO, Maria
2016Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic CaseSTECCHINI, M.; MACEDO, D.; REIS, A. C.; ABREU, A. P.; MOREIRA, A.; CASTRO, M.; KAISER, U.; LATRONICO, A. C.; ANTONINI, S.