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

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy

常染色体显性遗传WFS1相关视神经病变的特征及其与OPA1相关常染色体显性遗传视神经萎缩的比较

de Muijnck, Cansu; Haer-Wigman, Lonneke; van Everdingen, Judith A M; Lushchyk, Tanya; Heutinck, Pam A T; van Dooren, Marieke F; Kievit, Anneke J A; Verhoeven, Virginie J M; Simon, Marleen E H; Wasmann, Rosemarie A; Notting, Irene C; De Baere, Elfride; Walraedt, Sophie; De Zaeytijd, Julie; Van den Broeck, Filip; Leroy, Bart P; Boon, Camiel J F; van Genderen, Maria M

Leber's hereditary optic neuropathy like disease in MT-ATP6 variant m.8969G>A

MT-ATP6 变异 m.8969G>A 引起的 Leber 遗传性视神经病变样疾病

de Muijnck, Cansu; van Schooneveld, Mary J; Plomp, Astrid S; Rodenburg, Richard J; van Genderen, Maria M; Boon, Camiel J F

Evaluation of EphB4 as Target for Image-Guided Surgery of Breast Cancer

评估 EphB4 作为乳腺癌影像引导手术靶点的作用

Cansu de Muijnck, Yoren van Gorkom, Maurice van Duijvenvoorde, Mina Eghtesadi, Geeske Dekker-Ensink, Shadhvi S Bhairosingh, Alessandra Affinito, Peter J K Kuppen, Alexander L Vahrmeijer, Cornelis F M Sier