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Results 1-10 of 37 (Search time: 0.036 seconds).
| Issue Date | Title | Author(s) |
|---|---|---|
| 2013 | PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation | ARAUJO, Ricardo V.; CHANG, Claudia V.; CESCATO, Valter A. S.; FRAGOSO, Maria Candida B. V.; BRONSTEIN, Marcello D.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; CARVALHO, Luciani R. S. |
| 2013 | Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome | MONTENEGRO, Luciana Ribeiro; SILVEIRA, Leticia F. G.; TUSSET, Cintia; CASTRO, Margaret de; VERSIANI, Beatriz R.; LATRONICO, Ana Claudia; MENDONCA, Berenice Bilharinho; TRARBACH, Ericka B. |
| 2013 | Molecular and Gene Network Analysis of Thyroid Transcription Factor 1 (TTF1) and Enhanced at Puberty (EAP1) Genes in Patients with GnRH-Dependent Pubertal Disorders | CUKIER, Priscilla; WRIGHT, Hollis; RULFS, Tomke; SILVEIRA, Leticia Ferreira Gontijo; TELES, Milena Gurgel; MENDONCA, Berenice Bilharinho; ARNHOLD, Ivo J. P.; HEGER, Sabine; LATRONICO, Ana Claudia; OJEDA, Sergio R.; BRITO, Vinicius Nahime |
| 2011 | 46,XY Disorders of Sex Development (46,XY DSD) due to Androgen Receptor Defects: Androgen Insensitivity Syndrome | ARNHOLD, Ivo J. P.; MELO, Karla; COSTA, Elaine M. F.; DANILOVIC, Debora; INACIO, Marlene; DOMENICE, Sorahia; MENDONCA, Berenice B. |
| 2019 | Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR | NAKAGUMA, Marilena; CORREA, Fernanda A.; SANTANA, Lucas S.; BENEDETTI, Anna F. F.; V, Ricardo Perez; HUAYLLAS, Martha K. P.; MIRAS, Mirta B.; FUNARI, Mariana F. A.; LERARIO, Antonio M.; MENDONCA, Berenice B.; CARVALHO, Luciani R. S.; JORGE, Alexander A. L.; ARNHOLD, Ivo J. P. |
| 2018 | Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region | MACEDO, Delanie B.; FRANCA, Monica M.; MONTENEGRO, Luciana R.; CUNHA-SILVA, Marina; BESSA, Danielle S.; ABREU, Ana Paula; KAISER, Ursula B.; MENDONCA, Berenice B.; JORGE, Alexander A. L.; BRITO, Vinicius N.; LATRONICO, Ana Claudia |
| 2019 | Giant Prolactinoma Causing Hydrocephalus and Intracranial Hypertension as First Manifestations of Multiple Endocrine Neoplasia Type 1 | DANTAS, Naiara C. B.; SOARES, Carlos E. L.; MARTINS, Manoel R. A.; LOURENCO JR., Delmar M.; QUIDUTE, Ana R. P. |
| 2019 | Targeted sequencing identifies novel variants in common and rare MODY genes | SANTANA, Lucas S. de; CAETANO, Lilian A.; COSTA-RIQUETTO, Aline D.; FRANCO, Pedro C.; DOTTO, Renata P.; REIS, Andre F.; WEINERT, Leticia S.; SILVEIRO, Sandra P.; VENDRAMINI, Marcio F.; PRADO, Flaviene A. do; ABRAHAO, Giovanna C. P.; ALMEIDA, Ana Gregoria F. P. de; TAVARES, Maria da G. Rodrigues; GONCALVES, Wagner Rodrigo B.; SANTOMAURO JUNIOR, Augusto C.; HALPERN, Bruno; JORGE, Alexander A. L.; NERY, Marcia; TELES, Milena G. |
| 2012 | Surgical approach to medullary thyroid carcinoma associated with multiple endocrine neoplasia type 2 | TAVARES, Marcos R.; TOLEDO, Sergio P. A.; MONTENEGRO, Fabio L. M.; MOYSES, Raquel A.; TOLEDO, Rodrigo A.; SEKYIA, Tomoko; CERNEA, Claudio R.; BRANDAO, Lenine G. |
| 2012 | Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 | COUTINHO, Flavia L.; LOURENCO JR., Delmar M.; TOLEDO, Rodrigo A.; MONTENEGRO, Fabio L. M.; TOLEDO, Sergio P. A. |