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

Optimizing Lung Cancer Diagnostics: Insights from a Fast-Track Program in a Complex Healthcare Setting

优化肺癌诊断:来自复杂医疗环境中快速通道项目的启示

Scanagatta, Paolo; Bertolini, Alessandro; Naldi, Giuseppe; Antoniazzi, Francesca; Inzirillo, Francesco; Giorgetta, Casimiro Eugenio; Ravalli, Eugenio; Ancona, Gianluca; Cagnetti, Sara; Barbonetti, Claudio; Stangoni, Fabiano

Imerslund-Gräsbeck Syndrome in an Infant with a Novel Intronic Variant in the AMN Gene: A Case Report

一例携带AMN基因新型内含子变异的婴儿发生伊默斯伦德-格雷斯贝克综合征的病例报告

Pacitto, Alessandra; Prontera, Paolo; Stangoni, Gabriela; Stefanelli, Maurizio; Ceppi, Stefania; Cerri, Carla; Gurdo, Grazia; Mencarelli, Annalisa; Esposito, Susanna

Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene

Schilbach-Rott 综合征与 9q22.32q22.33 重复有关,涉及 PTCH1 基因

Prontera, Paolo; Rogaia, Daniela; Sallicandro, Ester; Mencarelli, Amedea; Imperatore, Valentina; Squeo, Gabriella Maria; Merla, Giuseppe; Elisei, Sandro; Moretti-Ferreira, Danilo; Esposito, Susanna; Stangoni, Gabriela

Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1

患有 1 型额顶鼻骨发育不全症的一个家庭中的神经母细胞瘤扩增序列基因突变

Eleonora Palagano, Giulia Zuccarini, Paolo Prontera, Renato Borgatti, Gabriela Stangoni, Sandro Elisei, Stefano Mantero, Ciro Menale, Antonella Forlino, Paolo Uva, Manuela Oppo, Paolo Vezzoni, Anna Villa, Giorgio R Merlo, Cristina Sobacchi

Epileptogenic Brain Malformations and Mutations in Tubulin Genes: A Case Report and Review of the Literature

致痫性脑畸形和微管蛋白基因突变:病例报告及文献综述

Mencarelli, Annalisa; Prontera, Paolo; Stangoni, Gabriela; Mencaroni, Elisabetta; Principi, Nicola; Esposito, Susanna