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Results 1-10 of 12 (Search time: 0.121 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. |
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 |
2015 | Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center | OTTO, Aline P.; FRANCA, Marcela M.; CORREA, Fernanda A.; COSTALONGA, Everlayny F.; LEITE, Claudia C.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; CARVALHO, Luciani R. S.; JORGE, Alexander A. L. |
2015 | Role of GLI2 in hypopituitarism phenotype | ARNHOLD, Ivo J. P.; FRANCA, Marcela M.; CARVALHO, Luciani R.; MENDONCA, Berenice B.; JORGE, Alexander A. L. |
2014 | Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort | LIDO, Andria C. V.; FRANCA, Marcela M.; CORREA, Fernanda A.; OTTO, Aline P.; CARVALHO, Luciani R.; QUEDAS, Elisangela P. S.; NISHI, Mirian Y.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; JORGE, Alexander A. L. |
2019 | DLK1 Is a Novel Link Between Reproduction and Metabolism | GAMES, Larissa G.; CUNHA-SILVA, Marina; CRESPO, Raiane P.; RAMOS, Carolina O.; MONTENEGRO, Luciana R.; CANTON, Ana; LEES, Melissa; SPOUDEAS, Helen; DAUBER, Andrew; MACEDO, Delanie B.; BESSA, Danielle S.; MACIEL, Gustavo A.; BARACAT, Edmund C.; JORGE, Alexander A. L.; MENDONCA, Berenice B.; BRITO, Vinicius N.; LATRONICO, Ana Claudia |
2019 | Exome Sequencing Reveals the POLR3H Gene as a Novel Cause of Primary Ovarian Insufficiency | FRANCA, Monica M.; HAN, Xingfa; FUNARI, Mariana F. A.; LERARIO, Antonio M.; NISHI, Mirian Y.; FONTENELE, Eveline G. P.; DOMENICE, Sorahia; JORGE, Alexander A. L.; GARCIA-GALIANO, David; ELIAS, Carol F.; MENDONCA, Berenice B. |
2020 | Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis | ROCHA-BRAZ, Manuela G. M.; FRANCA, Monica M.; FERNANDES, Adriana M.; LERARIO, Antonio M.; ZANARDO, Evelin A.; SANTANA, Lucas S. de; KULIKOWSKI, Leslie D.; MARTIN, Regina M.; MENDONCA, Berenice B.; FERRAZ-DE-SOUZA, Bruno |