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

Fungal meningoencephalitis caused by Phanerochaete sp.: Case report

由 Phanerochaete sp. 引起的真菌性脑膜脑炎:病例报告

Sánchez León, Juan Sebastián; Grasel, Michel Cristian; Severo, Cecília Bittencourt; Motta, Heryk; Vieira Reuwsaat, Júlia Catarina; Kmetzsch, Lívia; May, Guilherme Girardi; Petersen Behar, Paulo Renato; Pasqualotto, Alessandro C; Roberto de Mello Rieder, Carlos

Oncogene EVI1 drives acute myeloid leukemia via a targetable interaction with CTBP2

癌基因 EVI1 通过与 CTBP2 的可靶向相互作用驱动急性髓系白血病。

Dorien Pastoors ,Marije Havermans ,Roger Mulet-Lazaro ,Duncan Brian ,Willy Noort ,Julius Grasel ,Remco Hoogenboezem ,Leonie Smeenk ,Jeroen A A Demmers ,Michael D Milsom ,Tariq Enver ,Richard W J Groen ,Eric Bindels ,Ruud Delwel

The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?

有遗传性乳腺癌和卵巢癌风险的家族史:遗传咨询和检测的影响是什么?

Campacci, Natalia; Grasel, Rebeca Silveira; Galvão, Henrique de Campos Reis; Garcia, Lucas França; Ribeiro, Paula Carvalho; Pereira, Kercy Fram de Jesus de Sena; Goldim, José Roberto; Ashton-Prolla, Patricia; Palmero, Edenir Inêz

Optic neuritis and mydriasis after vaccination: a case report

接种疫苗后出现视神经炎和瞳孔散大:一例病例报告

Elcio Luiz Bonamigo, Pamela Kuyava, Taísa Sacomori Paula Zanotto Reginatto, Arthur Gabriel Duran, Luisa Truculo, Eglas Emanuel Rossi, Ricardo Alexandre Stock, Claudia Elisa Grasel

Cost-Effectiveness of BRCA 1/2 Genetic Test and Preventive Strategies: Using Real-World Data From an Upper-Middle Income Country

BRCA1/2基因检测和预防策略的成本效益:基于中高收入国家的真实世界数据

Lourenção, Marina; Simões Correa Galendi, Julia; Galvão, Henrique de Campos Reis; Antoniazzi, Augusto Perazzolo; Grasel, Rebeca Silveira; Carvalho, André Lopes; Mauad, Edmundo Carvalho; de Oliveira, Jorge Henrique Caldeira; Reis, Rui Manuel; Mandrik, Olena; Palmero, Edenir Inêz

Vestibular recruitment: new application for an old concept

前庭募集:旧概念的新应用

Bittar, Roseli Saraiva Moreira; Mezzalira, Raquel; Ramos, Alice Carolina Mataruco; Risso, Gabriel Henrique; Real, Danilo Martin; Grasel, Signe Schuster

Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer

对非BRCA1/BRCA2突变携带者进行全外显子组测序,这些患者罹患遗传性乳腺癌/卵巢癌的风险较高

Felicio, Paula S; Grasel, Rebeca S; Campacci, Natalia; de Paula, Andre E; Galvão, Henrique C R; Torrezan, Giovana T; Sabato, Cristina S; Fernandes, Gabriela C; Souza, Cristiano P; Michelli, Rodrigo D; Andrade, Carlos E; Barros, Bruna Durães De Figueiredo; Matsushita, Marcus M; Revil, Timothée; Ragoussis, Jiannis; Couch, Fergus J; Hart, Steven N; Reis, Rui M; Melendez, Matias E; Tonin, Patricia N; Carraro, Dirce M; Palmero, Edenir I

Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients

使用共分离和杂合性缺失分析来确定遗传性乳腺癌患者中未分类变异的致病性

Rebeca Silveira Grasel, Paula Silva Felicio, André Escremim de Paula, Natalia Campacci, Felipe Antônio de Oliveira Garcia, Edilene Santos de Andrade, Adriane Feijó Evangelista, Gabriela Carvalho Fernandes, Cristina da Silva Sabato, Pedro De Marchi, Cristiano de Pádua Souza, Cláudia Alessandra Andrad

A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58

2p14 中罕见的基因组重复是常染色体显性听力损失 DFNA58 的基础

Karina Lezirovitz, Gleiciele A Vieira-Silva, Ana C Batissoco, Débora Levy, Joao P Kitajima, Alix Trouillet, Ellen Ouyang, Navid Zebarjadi, Juliana Sampaio-Silva, Vinicius Pedroso-Campos, Larissa R Nascimento, Cindy Y Sonoda, Vinícius M Borges, Laura G Vasconcelos, Roberto M O Beck, Signe S Grasel, D

SUBJECTIVE SLEEP NEED AND DAYTIME SLEEPINESS IN ADOLESCENTS

青少年的主观睡眠需求和白天嗜睡情况

Geraldo Jose Ferrari Junior, Diego Grasel Barbosa, Rubian Diego Andrade, Andreia Pelegrini, Thais Silva Beltrame, Érico Pereira Gomes Felden