日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Interleukin-6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

白细胞介素-6作为面肩肱型肌营养不良症的关键生物标志物：来自纵向分析的证据

期刊:Annals of Clinical and Translational Neurology
影响因子:3.9
doi:10.1002/acn3.70210
Pini, Jonathan; Martinuzzi, Emanuela; Dhifallah, Sandra; Slioui, Abderhmane; Puma, Angela; Villa, Luisa; Cavalli, Michele; Ezaru, Andra; Garcia, Jérémy; Gambella, Manuela; Torre, Federico; Pavan, Luca Jacopo; Glaichenhaus, Nicolas; Sacconi, Sabrina
细胞生物学
发表日期：2026
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Co-Occurrence of Myasthenia Gravis and Facioscapulohumeral Muscular Dystrophy: A Case Series and Review of Literature

重症肌无力与面肩肱型肌营养不良症的共病：病例系列及文献综述

期刊:European Journal of Neurology
影响因子:3.9
doi:10.1111/ene.70477
Tammam, Giulia; Villa, Luisa; Lemmers, Richard J L F; Pini, Jonathan; Slioui, Abderhmane; Bouchareychas, Laura; David, Yann; Ioncea, Mihai-Bogdan; Salviati, Leonardo; Cavalli, Michele; Ezaru, Andra; Puma, Angela; Verschuuren, Jan J; van der Maarel, Silvère M; Sacconi, Sabrina
重症肌无力
免疫/内分泌
发表日期：2026
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French National Protocol for Diagnosis and Care of Calpainopathy (LGMD R1/LGMD D4): consensus guidelines for clinical practice

法国国家钙质沉着症诊断和治疗方案（LGMD R1/LGMD D4）：临床实践共识指南

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-026-04279-5
Severa, Gianmarco; Souvannanorath, Sarah; Tahiri, Iman; Alimi, Christophe; Slioui, Abderhmane; Villa, Luisa; Salort-Campana, Emmanuelle; Leturcq, France; Streichenberger, Nathalie; Krahn, Martin; Solé, Guilhem; Feasson, Léonard; Nadaj-Pakleza, Aleksandra; Tard, Celine; Stojkovic, Tanya; Sacconi, Sabrina; Malfatti, Edoardo
发表日期：2026
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Double trouble: a comprehensive study into unrelated genetic comorbidities in adult patients with Facioscapulohumeral Muscular Dystrophy Type I

双重困扰：一项针对I型面肩肱型肌营养不良症成年患者无关遗传合并症的综合研究

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-024-01770-0
Puma, Angela; Tammam, Giulia; Ezaru, Andra; Slioui, Abderhmane; Torchia, Eleonora; Tasca, Giorgio; Villa, Luisa; Cavalli, Michele; Salviati, Leonardo; van der Vliet, Patrick J; Lemmers, Richard Jlf; Pini, Jonathan; van der Maarel, Silvère M; Sacconi, Sabrina
发表日期：2025
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Toward European harmonization of national myasthenia gravis registries: modified Delphi procedure-based expert consensus on collectable data

迈向欧洲各国重症肌无力登记系统协调统一：基于改进的德尔菲法的专家共识，探讨可收集数据

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-024-03520-3
Slioui, Abderhmane; Tammam, Giulia; Vanoli, Fiammetta; Marina, Adela Della; Vohanka, Stanislav; Gilhus, Nils Erik; Moroni, Isabella; Leite, Maria Isabel; Piehl, Fredrik; Antozzi, Carlo; Pini, Jonathan; Stascheit, Frauke; Attarian, Shahram; Santos, Ernestina; Verschuuren, Jan; Canonge, Lou; Garcia, Jeremy; Perriard, Caroline; Cortés-Vicente, Elena; Mantegazza, Renato; Meisel, Andreas; Sacconi, Sabrina
重症肌无力
免疫/内分泌
发表日期：2025
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Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry

FSHD1患者罕见特征的患病率和预测因素：来自法国FSHD注册研究的启示

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-03877-z
Sanson, Benoît; Slioui, Abderhmane; Garcia, Jérémy; Klouvi, Lori; Lejeune, Julie; Stalens, Caroline; Guien, Céline; Rabarimeriarijaona, Sitraka; Bernard, Rafaëlle; Nectoux, Juliette; Attarian, Sharham; Bédat-Millet, Anne-Laure; Bouhour, Françoise; Boyer, François Constant; Chanson, Jean-Baptiste; Choumert, Ariane; Cintas, Pascal; De La Cruz, Elisa; Féasson, Léonard; Fournier, Maxime; Ghorab, Karima; Jacquin-Piques, Agnès; Laforêt, Pascal; Magot, Armelle; Michaud, Maud; Noury, Jean-Baptiste; Solé, Guilhem; Spinazzi, Marco; Stojkovic, Tanya; Tard, Céline; Villa, Luisa; Béroud, Christophe; Sacconi, Sabrina
FSH
发表日期：2025
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