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Angela Berardinelli

KU Leuven
H指数:51
被引数:7,459

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Reducing Early-Life Smoke Exposure as a Preventive Strategy for Pediatric Multiple Sclerosis: Results from the PEDIGREE Study

将早期生命期烟雾暴露作为儿童多发性硬化预防策略:PEDIGREE研究的结果

2026-02-180
OAAI
Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies
2025-12-010
OAAI
Landscape Analysis of COL6A1, COL6A2, and COL6A3 Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report

COL6A1、COL6A2和COL6A3致病性变异在呈现VI型胶原蛋白相关肌病的大型意大利队列中的景观分析:一项全国性报告

2025-10-080
OAAI
Upper limb progression in Duchenne muscular dystrophy: Insights from a 36-month longitudinal study using the PUL 20

杜氏肌营养不良症上肢进展:基于36个月纵向研究使用PUL 20的见解

2025-09-180
OA
Quantitative cervical cord MRI in spinal muscular atrophy: a sensitive imaging biomarker of disease evolution and treatment

脊髓性肌萎缩症中定量颈椎脊髓MRI:一种敏感的疾病演变和治疗成像生物标志物

2025-06-240
OAAI
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey

意大利杜氏肌营养不良症的患病率: 一项全国性调查

2024-12-160
PRE
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity

贝克肌营养不良的自然史:DMD基因突变预测临床严重程度

BRAIN
IF11.7
2024-11-050
PRE
Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1-Results from a Retrospective Analysis in Italy

1型强直性肌营养不良儿童报告的睡眠障碍与行为问题之间的关联-意大利回顾性分析的结果

2024-09-140
OAAI
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?

具有四个SMN2拷贝的儿童和成人脊髓性肌萎缩症患者的临床表型: 它们真的都稳定吗?

2023-09-2212
OAAI
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?

动态和非动态Duchenne肌营养不良症患者PUL 2.0域的纵向分析: 它们与功能能力的关系如何变化?

2023-04-123
OAAI
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies An Italian Nationwide Survey

意大利全国性调查显示,在疾病缓解疗法时代,脊髓性肌萎缩症的患病率

2023-03-1414
OAAI
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease

成人脊髓性肌萎缩症: 一项大规模自然史研究显示性别对疾病的影响

2022-10-1113
PRE
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

扩大具有核心和微型核心的RYR1-related先天性肌病的临床病理和遗传谱: 一项意大利人口研究

2022-04-1510
OAAI
6MWT as measure of motor function and endurance in SMA type 3 patients treated with nusinersen
2021-10-010
PRE