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Armelle Magot

centre de référence des maladies neuromusculaires aoc
H指数:30
被引数:3,150

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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
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study

肢带型肌营养不良与TRIM32变异相关:一项全国队列研究

2026-04-060
PRE
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
SMCHD1 genetic variants in type 2 facioscapulohumeral dystrophy and challenges in predicting pathogenicity and disease penetrance
2024-12-260
PRE
Spinal muscular atrophy is also a disorder of spermatogenesis
2024-12-200
OAAI
Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis
BRAIN
IF11.7
2024-05-021
OAAI
Multidisciplinary team meetings in treatment of spinal muscular atrophy adult patients: a real-life observatory for innovative treatments

脊髓性肌萎缩症成人患者治疗中的多学科团队讨论会:创新疗法的真实世界观察研究

2024-01-244
OAAI
Characteristics of Patients With Late-Onset Pompe Disease in France
2023-08-293
OA
Convergence of patient-and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy
2022-03-023
OAAI
Human MuStem cells repress T-cell proliferation and cytotoxicity through both paracrine and contact-dependent pathways
2022-01-104
OAAI
A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases
2021-10-2610
OAAI
A recurrent RYR1 mutation associated with early-onset hypotonia and benign disease course
2021-09-175
OAAI
Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders
2021-09-016
OAAI