日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Single-session music therapy reduces anxiety and depression among hospitalized adults in an endocrinology ward

单次音乐疗法可减轻内分泌病房住院成年患者的焦虑和抑郁。

Lima, Veronique; Rios, Izabel Cristina; Inacio, Marlene; Brito, Vinicius Nahime; Mendonca, Berenice B

SUN-465 A Rare Germline Loss-of-Function Variant in the Pyruvate Dehydrogenase Phosphatase Catalytic Subunit 2 Gene in a Patient with Abdominal Paraganglioma

SUN-465:腹部副神经节瘤患者丙酮酸脱氢酶磷酸酶催化亚基 2 基因中罕见的种系功能缺失变异

O'Halloran, Ken D; Iturriaga, Rodrigo; Rocher, Asuncion; Couto, Blas; Pinto, María Jose Angel; Avale, Maria‐Elena; Falzone, Tomas; Gershanik, Oscar; Chade, Anabel; Mizraji, Gabriel; Gonzalez‐Toledo, Maria Eugenia; Peralta, Maria; Gomez‐Arevalo, Gonzalo; Mezmezian, Monica; Marras, Connie; Sevlever, Gustavo; Freitas-Castro, Felipe; Cardoso Fagundes, Gustavo Freitas; Santana, Lucas Santos; Afonso, Ana Caroline F; Ledesma, Felipe L; Soares, Ibere C; Mendonca, Berenice B; Latronico, Ana Claudia; Almeida, Madson Q

SLC25A11, a Novel Gene Associated With Carney-Stratakis Syndrome.

SLC25A11,一种与卡尼-斯特拉塔基斯综合征相关的新基因

Freitas-Castro Felipe, Santana Lucas S, Fagundes Gustavo F C, Lobato Eduardo C, Afonso Ana Caroline F, Nakamura Izabel T, Ledesma Felipe L, Soares Ibere C, Mendonca Berenice B, Latronico Ana Claudia, Stratakis Constantine A, Almeida Madson Q

Pathogenicity of germline VHL variants is associated with renal cell carcinoma size in von Hippel-Lindau disease.

生殖系 VHL 变异的致病性与 von Hippel-Lindau 病中的肾细胞癌大小相关

Mori Gustavo H, Fagundes Gustavo F C, Santana Lucas S, Freitas-Castro Felipe, Afonso Ana Caroline F, Lourenço Delmar M Jr, Pereira Maria Adelaide A, Tanno Fabio Y, Srougi Victor, Chambo Jose L, Cordeiro Mauricio D, Nahas William C, Hoff Ana O, Fragoso Maria Candida B V, Mendonca Berenice B, Latronico Ana Claudia, Almeida Madson Q

MON-295 Histopathological Evaluation (HISTALDO) Predicts Outcome in Unilateral Primary Aldosteronism

MON-295 组织病理学评估 (HISTALDO) 可预测单侧原发性醛固酮增多症的预后

Pasqua, Analia V; Mazza, Oscar M; Goldbaum, Tatiana Silva; Ledesma, Felipe L; Guimaraes, Augusto G; Okubo, Jessica; Kawahara, Eduardo Z; Calsavara, Vinicius; Bortolloto, Luiz A; Chambo, Jose L; Villares Fragoso, Maria Candida Barisson; Pereira, Maria Adelaide A; Pio-Abreu, Andrea; Silva, Giovanio V; Silveira, Joao V; Consolim-Colombo, Fernanda; Drager, Luciano F; Nahas, William C; Latronico, Ana Claudia; Mendonca, Berenice B; Almeida, Madson Q; Zerbini, Maria Claudia N

Intraoperative radiofrequency ablation for unresectable abdominal paraganglioma: a case report

术中射频消融治疗无法切除的腹部副神经节瘤:病例报告

Magalhaes, Isabelle P A; Boger, Bibiana D; Gomes, Nathalia L; Martins, Guilherme L P; Bomfim, Leomarques A Jr; Fagundes, Gustavo F C; Rocha, Roberta S; Coelho, Fernando M A; Chambo, Jose L; Latronico, Ana Claudia; Fragoso, Maria Candida B V; Hoff, Ana O; Mendonca, Berenice B; Menezes, Marcos R; Almeida, Madson Q

Clinical and Pathological Predictors of Death for Adrenocortical Carcinoma

肾上腺皮质癌死亡的临床和病理预测因素

Pato, Eduardo; Srougi, Victor; Zerbini, Claudia; Ledesma, Felipe L; Tanno, Fabio; Almeida, Madson Q; Nahas, William; Latronico, Ana Claudia; Mendonca, Berenice B; Chambô, Jose L; Fragoso, Maria Candida B V

Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

贝克威思-威德曼综合征在新生儿筛查中表现为与经典型先天性肾上腺皮质增生症相似的症状

Martins, Jéssica Mallmann Erbes Schaefer; Braga, Barbara Leitao; Sampaio, Klevia Nunes Feitosa; de Souza Garcia, Tamires; Van de Sande Lee, Juliana; Cechinel, Edson; Simoni, Genoir; Nascimento, Marilza Leal; da Silva, Paulo Cesar Alves; Fragoso, Maria C V; Bachega, Tania A A S; Nishi, Mirian Y; Mendonca, Berenice B

8712 Pediatric Adrenocortical Oncocytic Neoplasm With Central Precocious Puberty: A Case Report

8712 伴有中枢性性早熟的儿童肾上腺皮质嗜酸性肿瘤:病例报告

Conwell, Louise S; Huzita, Claudia H; Lins, Wallison M; Beeby, Stephanie K; Lopes, Roberto I; Denes, Francisco T; Claudia Latronico, Ana; Polo, Marilia; Victor, Carolina R; Hoff, Ana A; Mendonca, Berenice B; Almeida, Madson Q; Barisson Villares Fragoso, Maria Candida

Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study

MECP2基因罕见变异与中枢性性早熟女孩的关系:一项转化队列研究

Canton, Ana P M; Tinano, Flávia R; Guasti, Leonardo; Montenegro, Luciana R; Ryan, Fiona; Shears, Deborah; de Melo, Maria Edna; Gomes, Larissa G; Piana, Mariana P; Brauner, Raja; Espino-Aguilar, Rafael; Escribano-Muñoz, Arancha; Paganoni, Alyssa; Read, Jordan E; Korbonits, Márta; Seraphim, Carlos E; Costa, Silvia S; Krepischi, Ana Cristina; Jorge, Alexander A L; David, Alessia; Kaisinger, Lena R; Ong, Ken K; Perry, John R B; Abreu, Ana Paula; Kaiser, Ursula B; Argente, Jesús; Mendonca, Berenice B; Brito, Vinicius N; Howard, Sasha R; Latronico, Ana Claudia