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

Second-Generation RT-QuIC Assay for the Diagnosis of Creutzfeldt-Jakob Disease Patients in Brazil

巴西用于诊断克雅氏病患者的第二代RT-QuIC检测

Barbosa, Breno José Alencar Pires; Castrillo, Bruno Batitucci; Alvim, Ricardo Pires; de Brito, Marcelo Houat; Gomes, Helio R; Brucki, Sônia M D; Smid, Jerusa; Nitrini, Ricardo; Landemberger, Michele C; Martins, Vilma R; Silva, Jerson L; Vieira, Tuane C R G

First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease

巴西一名克雅氏病患者首次发现V180I罕见突变

De Souza, Ricardo Krause Martinez; Josviak, Nalini Drieli; Batistela, Meire Silva; Santos, Paulo Sergio Faro; Landemberger, Michele Christine; Ramina, Ricardo

Disease-associated mutations in the prion protein impair laminin-induced process outgrowth and survival

朊病毒蛋白中与疾病相关的突变会损害层粘连蛋白诱导的突起生长和存活。

Machado, Cleiton F; Beraldo, Flavio H; Santos, Tiago G; Bourgeon, Dominique; Landemberger, Michele C; Roffé, Martin; Martins, Vilma R

Prion diseases are undercompulsory notification in Brazil: Surveillance of cases evaluated by biochemicaland/or genetic markers from 2005 to 2007

在巴西,朊病毒疾病并非强制报告:2005年至2007年间,通过生化和/或遗传标记评估的病例监测结果

Martins, Vilma Regina; Gomes, Hélio Rodrigues; Chimelli, Leila; Rosemberg, Sergio; Landemberger, Michele Christine

Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil

巴西一例与朊病毒蛋白基因200号密码子错义突变相关的克雅氏病

Smid, Jerusa; Martins, Vilma Regina; Landemberger, Michele Christine; Riva, Daniele; Anghinah, Renato; Nitrini, Ricardo