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Pascal Cintas

referral center for neuromuscular diseases
H指数:29
被引数:3,663

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Rituximab With or Without Chemotherapy for Anti-MAG Neuropathy: A Retrospective Multicenter Real-World Study

利妥昔单抗联合或不联合化疗治疗抗-MAG神经病的回顾性多中心真实世界研究

2026-10-010
PRE
Subtype-specific mortality in idiopathic inflammatory myopathies: A hospital-based cohort

特发性炎症性肌病中的分型特异性死亡率:一项基于医院的队列研究

2026-08-010
PRE
A qualitative study of the discrepancy between patient expectations and assessment practices in 5q-adult spinal muscular atrophy in France

对法国5q型成人脊髓性肌萎缩症患者期望与评估实践差异的定性研究

2026-04-240
PRE
Real-world effectiveness and safety of zilucoplan in patients with anti-AChR myasthenia gravis: A retrospective cohort study in France

在抗乙酰胆碱受体(anti-AChR)重症肌无力患者中,zilucoplan的实效性与安全性:一项法国回顾性队列研究

2026-03-290
PRE
Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case Series

人微小病毒B19感染继发多发性单神经病变:病例系列研究

2026-03-010
OAAI
Causes of Death and Comorbidities in Adult Patients With Late-Onset Pompe Disease: A French Pompe Registry Retrospective Study

成人迟发性庞贝病患者死亡原因及合并症:一项法国庞贝注册登记研究

2025-10-270
OAAI
Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR)

罕见神经肌肉疾病患者的诊断困境与诊断延迟:来自法国罕见神经肌肉疾病国家网络(FILNEMUS)和法国国家罕见病数据库(BNDMR)的患者特征洞察

2025-09-010
OAAI
Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy

全国范围内103例SH3TC2基因相关脱髓鞘周围神经病的表型和基因型特征分析

2025-07-310
OA
Spectrum of Phenotypes in SMA Patients With 4 SMN2 Copies in the French Population
2025-04-010
OAAI
SMCHD1 genetic variants in type 2 facioscapulohumeral dystrophy and challenges in predicting pathogenicity and disease penetrance
2024-12-260
PRE
Caffeine consumption outcomes on amyotrophic lateral sclerosis disease progression and cognition

咖啡因摄入对肌萎缩侧索硬化疾病进展和认知的影响

2024-09-012
OAAI
Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis
BRAIN
IF11.7
2024-05-021
OAAI