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

Tracing neuropathological signatures: TARDBP and C9orf72 double mutations in a Sicilian family

追踪神经病理学特征:西西里家族中的TARDBP和C9orf72双突变

Masrori, Pegah; Tomé, Sandra O; Dedeene, Lieselot; Remiche, Gauthier; Van Esch, Hilde; Thal, Dietmar Rudolf; Van Damme, Philip

Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient-reported outcome measures

对未来贝克尔肌营养不良症成人临床试验的启示:通过肌肉磁共振成像、临床和患者报告结局指标检测疾病进展

De Wel, Bram; Iterbeke, Louise; Huysmans, Lotte; Peeters, Ronald; Goosens, Veerle; Dubuisson, Nicolas; van den Bergh, Peter; Van Parijs, Vinciane; Remiche, Gauthier; De Waele, Liesbeth; Maes, Frederik; Dupont, Patrick; Claeys, Kristl G

Recommendations for the management of myasthenia gravis in Belgium

比利时重症肌无力管理建议

De Bleecker, Jan L; Remiche, Gauthier; Alonso-Jiménez, Alicia; Van Parys, Vinciane; Bissay, Véronique; Delstanche, Stéphanie; Claeys, Kristl G

A First Case of Acute Flaccid Myelitis Related to Enterovirus D68 in Belgium: Case Report

比利时首例与肠道病毒D68相关的急性弛缓性脊髓炎病例报告

Rodesch, Marine; Sculier, Claudine; Lolli, Valentina; Remiche, Gauthier; Delpire, Iris; Fricx, Christophe; Vermeulen, Françoise; Christiaens, Florence

A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium

比利时一项回顾性调查,研究对象为在真实临床实践中使用帕替西兰治疗的遗传性转甲状腺素蛋白介导的(hATTR)淀粉样变性患者。

De Bleecker, Jan L; Claeys, Kristl G; Delstanche, Stéphanie; Van Parys, Vinciane; Baets, Jonathan; Tilleux, Sébastien; Remiche, Gauthier

Antenatal Membranous Nephropathy and Type 2 (Axonal) Charcot-Marie-Tooth With Mutations in the Metallo-Membrane Endopeptidase Gene: A Call for Family Screening and Pharmacovigilance

产前膜性肾病和2型(轴索型)夏科-马里-图斯病伴金属膜内肽酶基因突变:呼吁开展家族筛查和药物警戒

Nortier, Joëlle L; Remiche, Gauthier; Delrée, Paul; Nauta, Jeroen; Notermans, Nicolette C; Vivarelli, Marina; Diodato, Daria; Solé, Guilhem; Debiec, Hanna; Ronco, Pierre

Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation

由AIFM1基因突变引起的共济失调、神经病变、听力丧失和智力障碍

Pandolfo, Massimo; Rai, Myriam; Remiche, Gauthier; Desmyter, Laurence; Vandernoot, Isabelle

Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures

比利时晚发型庞贝病(LOPD):临床特征和预后指标

Vanherpe, P; Fieuws, S; D'Hondt, A; Bleyenheuft, C; Demaerel, P; De Bleecker, J; Van den Bergh, P; Baets, J; Remiche, G; Verhoeven, K; Delstanche, S; Toussaint, M; Buyse, B; Van Damme, P; Depuydt, C E; Claeys, K G

Acute Paraparesis after Epidural Corticosteroid Injection Revealing Spinal Dural Arteriovenous Fistula in a HIV Patient

HIV患者硬膜外皮质类固醇注射后出现急性截瘫,病理诊断为脊髓硬膜动静脉瘘

Le Goueff, Anouk; Mavroudakis, Nicolas; Mine, Benjamin; De Witte, Olivier; Remiche, Gauthier