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Results 1-10 of 22 (Search time: 0.004 seconds).
| Issue Date | Title | Author(s) |
|---|---|---|
| 2014 | Fatal Factitious Cushing's Syndrome (Munchhausen's syndrome) in a Patient with a Prolactinoma and Silent Corticotrophinoma: Case Report and Literature Review | MINANNI, Carlos Andre; CARDOSO, Ana Luiza de Almeida; ALBUQUERQUE, Edoarda Vasco de Albuquerque; LOPES, Ludmilla Malveira Lima; GLEZER, Andrea; VERDUGUEZ, Elisa Del Rosario Ugarte; GALLUCCI-NETO, Jose; GATTAZ, Wagner Farid; MENDONCA, Berenice B.; BRONSTEIN, Marcello D.; MACHADO, Marcia Carlos; FRAGOSO, Maria Candida Barisson Villares |
| 2014 | Inherited Autosomal Dominant Mutations in ARMC5 Gene a Frequent Cause of Primary Macronodular Adrenal Hyperplasia | ALENCAR, Guilherme Asmar; LERARIO, Antonio M.; NISHI, Mirian Yumie; MARIANI, Beatriz M. P.; ALMEIDA, Madson Q.; TREMBLAY, Johanne; HAMET, Pavel; BOURDEAU, Isabelle; ZERBINI, Maria Claudia N.; PEREIRA, Maria Adelaide Albergaria; GOMES, Gilberto Carlos; ROCHA, Manoel Souza; CHAMBO, Jose Luiz; LACROIX, Andre; MENDONCA, Berenice B.; FRAGOSO, Maria Candida Barisson Villares |
| 2014 | Mutation and Expression Analysis of DICER1 and Mir-103 in Pediatric and Adult Adrenocortical Tumors | SOUSA, Gabriela R. V.; RIBEIRO, Tamaya C.; FARIA, Andre M.; MARIANI, Beatriz M. P.; LERARIO, Antonio M.; ZERBINI, Maria Claudia N.; SOARES, Ibere C.; WAKAMATSU, Alda; ALVES, Venancio A. F.; MENDONCA, Berenice B.; FRAGOSO, Maria Candida B. V.; LATRONICO, Ana Claudia; ALMEIDA, Madson Q. |
| 2014 | A Novel OTX2 Mutation, p.H230L, Causes Hypopituitarism with Incomplete Penetrance: Exome Sequencing to Identify Modifier Genes | FOYOUZI, Nastaran; CAMPER, Sally Ann; MOREIRA, Michele; FRANCA, Marcela M.; OTTO, Aline P.; CORREA, Fernanda de Azevedo; ARNHOLD, Ivo J. P.; MENDONCA, Berenice B.; MA, Qianyi; LI, Jun Z.; FANG, Qing; CARVALHO, Luciani R. S. |
| 2014 | Inherited Digenic Missense Variants in FGFR2 and MAP3K1 Genes in Two Siblings with 46,XY Partial Gonadal Dysgenesis | MACHADO, Aline Zamboni; NISHI, Mirian Yumie; COSTA, Elaine Maria Frade; MENDONCA, Berenice B.; DOMENICE, Sorahia |
| 2014 | High Frequency of Subclinical Cushing's Syndrome in the Inherited Autosomal Dominant Primary Macronodular Adrenal Hyperplasia Due to ARMC5 Mutations | ALENCAR, Guilherme Asmar; ALMEIDA, Madson Q.; LERARIO, Antonio Marcondes; RESENDE, Gabriela; NISHI, Mirian Yumie; PEREIRA, Maria Adelaide Albergaria; MENDONCA, Berenice B.; FRAGOSO, Maria Candida B. V. |
| 2014 | Improving the Effectiveness of CAH Newborn Screening Adjusting 17OHP Levels According to Degree of Prematurity and Age at Sample Collection | CARYALHO, Daniel Fiordelisio de; HAYASHI, Giselle Yuri; FAURE, Claudia; VALLEJOS, Carla Gabriella; BRITO, Vinicius N.; MENDONCA, Berenice B.; BACHEGA, Tania A. |
| 2014 | Sorafenib Treatment Improves Refractory Hypercalcemia in a Patient with Metastatic Parathyroid Carcinoma: A Case Report | LERARIO, Antonio M.; MARTIN, Regina M.; HOFF, Ana Oliveira; NAKAGUMA, Marilena; CASTRO, Gilberto; TEIXEIRA, Carlos Henrique; MENEZES, Marcos; DALALIO, Vanessa; MENDONCA, Berenice B. |
| 2014 | Analysis of Predictive Factors for Low Bone Mineral Density in Young Adults with 21-Hydroxylase Deficiency | TAVARES, Maria da Glori; ALVARENGA, Tassiane; MOREIRA, Ricardo Paranhos; CARVALHO, Daniel Fiordelisio de; GOMES, Larissa Garcia; MADUREIRA, Guiomar; MENDONCA, Berenice B.; BACHEGA, Tania A. |
| 2014 | Image-Guided Percutaneous Cryoablation of Sclerotic Bone Metastases from Adrenocortical Carcinoma: A New Approach to a Multimodality Palliative Care | FREITAS, Ricardo Miguel Costa de; FRAGOSO, Maria Candida Barisson Villares; LERARIO, Antonio M.; BEZERRA NETO, Joao Evangelista; ALMEIDA, Cristiane Maria; MENDONCA, Berenice B.; GANGI, Afshin |
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