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Anthony Béhin

Sorbonne Universite
H指数:51
被引数:8,787

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T-Cell Acute Lymphoblastic Leukemia in a Young Patient With Andersen-Tawil Syndrome Successfully and Safely Treated With Intensive Chemotherapy Including Potential Precipitating Drugs: A Case Report After 3.5 Years of Follow-up

T细胞急性淋巴细胞白血病合并 Andersen-Tawil 综合征的年轻患者,经包含潜在诱发药物的大剂量化疗成功且安全治疗:随访3.5年的病例报告

2026-05-270
OAAI
Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review

揭示MYH2相关肌病:来自病例系列和系统综述的组织学-遗传学见解

2025-11-180
OA
Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA)

X连锁过度自噬肌病(XMEA)患者的临床、形态学和分子特征

2025-11-010
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
MYH7-related myopathies: clinical, myopathological and genotypic spectrum in a multicentre French cohort
2024-10-240
OAAI
CRITICAL CONTRIBUTION OF MITOCHONDRIA IN THE DEVELOPMENT OF CARDIOMYOPATHY LINKED TO DESMIN MUTATION

线粒体在与DESMIN突变相关的心肌病发展中的关键贡献

2024-06-015
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
Critical contribution of mitochondria in the development of cardiomyopathy linked to desmin mutation

线粒体在与desmin突变相关的心肌病发展中的关键贡献

2024-01-025
OAAI
Characteristics of Patients With Late-Onset Pompe Disease in France
2023-08-293
OA
Prognosis of Right Ventricular Systolic Dysfunction in Patients With Duchenne Muscular Dystrophy

Duchenne型肌营养不良患者右心室收缩功能障碍的预后

2023-08-153
OAAI
Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy
2023-08-016
OAAI
Hypersensitivity infusion-associated reactions induced by enzyme replacement therapy in a cohort of patients with late-onset Pompe disease: An experience from the French Pompe Registry
2023-07-013
OAAI
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort
BRAIN
IF11.7
2023-03-133
OA