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Results 1-10 of 13 (Search time: 0.055 seconds).
| Issue Date | Title | Author(s) |
|---|---|---|
| 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. |
| 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. |
| 2018 | Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient | CAMARGO, Rosalinda Yasato; KANAMURA, Cristina Takami; FRIGUGLIETTI, Celso Ubirajara; NOGUEIRA, Celia Regina; IORCANSKY, Sonia; TINCANI, Alfio Jose; BEZERRA, Ana Karina; BRUST, Ester; KOYAMA, Fernanda Christtanini; CAMARGO, Anamaria Aranha; REGO, Fernanda Orpinelli R.; GALANTE, Pedro Alexandre Favoretto; MEDEIROS-NETO, Geraldo; RUBIO, Ileana Gabriela Sanchez |
| 2011 | Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism | TUSSET, Cintia; TRARBACH, Ericka B.; SILVEIRA, Leticia Ferreira Gontijo; BENEDUZZI, Daiane; MONTENEGRO, Luciana; LATRONICO, Ana Claudia |
| 2015 | Differential expression of genes encoding proteins of the HGF/MET system in insulinomas | MURAT, Cahue de Bernardis; ROSA, Paula Waki Lopes da; FORTES, Maria Angela Henriques Zanella; CORREA, Luciana; MACHADO, Marcel Cerqueira Cesar; NOVAK, Estela Maria; SIQUEIRA, Sheila Aparecida Coelho; PEREIRA, Maria Adelaide Albergaria; CORREA-GIANNELLA, Maria Lucia; GIANNELLA-NETO, Daniel; GIORGI, Ricardo Rodrigues |
| 2018 | Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1 | MARX, Stephen J.; LOURENCO JR., Delmar M. |
| 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 |
| 2022 | Delayed Puberty Phenotype Observed in Noonan Syndrome Is More Pronounced in Girls than Boys | REZENDE, Raissa C.; NORONHA, Renata Maria; KESELMAN, Ana; QUEDAS, Elisangela P. S.; DANTAS, Naiara C. B.; ANDRADE, Nathalia L. M.; BERTOLA, Debora R.; MALAQUIAS, Alexsandra C.; JORGE, Alexander A. L. |
| 2023 | Clinical and Genetic Characterization of Familial Central Precocious Puberty | TINANO, Flavia Rezende; CANTON, Ana Pinheiro Machado; MONTENEGRO, Luciana R.; LEAL, Andrea de Castro; FARIA, Aline G.; SERAPHIM, Carlos E.; BRAUNER, Raja; JORGE, Alexander A.; MENDONCA, Berenice B.; ARGENTE, Jesus; BRITO, Vinicius N.; LATRONICO, Ana Claudia |
| 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 |