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Antonella Pini

irccs istituto delle scienze neurologiche di bologna
H指数:38
被引数:4,458

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Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24-Month Follow-Up From the Italian Registry

Onasemnogene Abeparvovec 在I型脊髓性肌萎缩症中的研究:来自意大利登记系统的24个月随访结果

2026-03-190
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
Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts

致纤维化分子在CRISPR编辑的Emery–Dreifuss肌营养不良成纤维细胞中减少

2025-08-270
OA
Clinical Characterization of a Multicenter International Cohort of Patients With Aicardi-Goutières Syndrome Homozygous for the RNASEH2B:p.Ala177Thr Variant: Early Clinical Markers of Disease Severity

Aicardi-Goutières综合征患者(RNASEH2B基因p.Ala177Thr变异纯合子)的多中心国际队列的临床特征:疾病严重程度的早期临床标志物

2025-07-250
OAAI
Patients on treatment with risdiplam in Italy: challenges in the interpretation of the real-world data

意大利接受risdiplam治疗的患者的真实世界数据解读挑战

2025-03-281
PRE
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
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
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation
2024-02-273
OAAI
Onasemnogene abeparvovec in spinal muscular atrophy : predictors of efficacy and safety in naive patients with spinal muscular atrophy and following switch from other therapies

脊髓性肌萎缩症中的Onasemnogene abeparvovec: 幼稚的脊髓性肌萎缩症患者和从其他疗法转换后的疗效和安全性的预测因子

2023-05-0119
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
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
Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Duchenne肌营养不良症呼吸功能的遗传修饰

2020-04-2834
OA
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutieres Syndrome Cohort: Report of 12 New Cases and Literature Review

意大利Aicardi Goutieres综合征队列的分子遗传学和干扰素特征: 12例新病例报告和文献综述

2019-05-2632
OAAI
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1

进行性肌阵挛性癫痫相关的脊髓性肌萎缩症: 由ASAH1突变引起的罕见疾病

2015-04-0339
OAAI