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

Diagnostic Criteria and Management of MELAS and Stroke-Like Episodes: Consensus-Based Statements

MELAS 和卒中样发作的诊断标准和管理:基于共识的声明

Mancuso, Michelangelo; Bellusci, Marcello; Carelli, Valerio; de Coo, Irenaeus; Diodato, Daria; Distelmaier, Felix; Hikmat, Omar; Hirano, Michio; Horvath, Rita; Karaa, Amel; Klopstock, Thomas; Koenig, Mary Kay; Kornblum, Cornelia; La Morgia, Chiara; Lopriore, Piervito; Martikainen, Mika Henrik; McFarland, Robert; Musumeci, Olimpia; Pitceathly, Robert D S; Primiano, Guido; Rahman, Shamima; Scaglia, Fernando; Schaefer, Andrew; Schiff, Manuel; Semmler, Luisa; Lamperti, Costanza; Servidei, Serenella

Cross-cultural adaptation of the Italian version of the "Child and Youth Mental Health Instrument for Developmental Disabilities" (I-ChYMH-DD)

“儿童和青少年发育障碍心理健康评估工具”(I-ChYMH-DD)意大利语版的跨文化适应性研究

Sforza, Elisabetta; Leoni, Chiara; De Rosa, Elena; Bellani, Jacopo; Viscogliosi, Germana; Di Paola, Antonella; Zampino, Marta; Fischetto, Rita; Pane, Marika; Rigante, Donato; Servidei, Serenella; Primiano, Guido; Onesimo, Roberta; Carfì, Angelo; Giuseppe, Zampino

Author Correction: Macrophages excite muscle spindles with glutamate to bolster locomotion

作者更正:巨噬细胞利用谷氨酸兴奋肌梭,从而增强运动能力

Yan, Yuyang; Antolin, Nuria; Zhou, Luming; Xu, Luyang; Vargas, Irene Lisa; Gomez, Carlos Daniel; Kong, Guiping; Palmisano, Ilaria; Yang, Yi; Chadwick, Jessica; Müller, Franziska; Bull, Anthony M J; Lo Celso, Cristina; Primiano, Guido; Servidei, Serenella; Perrier, Jean François; Bellardita, Carmelo; Di Giovanni, Simone

Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8

由MT-ATP6和MT-ATP8致病变异引起的线粒体ATPase缺乏症患者的自然病程

Carli, Sara; Levarlet, Anna; Diodato, Daria; Bertini, Enrico Silvio; Martinelli, Diego; Malandrini, Alessandro; Lopergolo, Diego; Gallus, Gian Nicola; Ganetzky, Rebecca D; La Morgia, Chiara; Carelli, Valerio; Primiano, Guido; Domínguez-González, Cristina; Serrano-Lorenzo, Pablo; Martín, Miguel A; Ardissone, Anna; Lamperti, Costanza; Nicoletta, Valeria; Klopstock, Thomas; Distelmaier, Felix; Zeng, Leopold; Büchner, Boriana; Mancuso, Michelangelo; Schuelke, Markus; Prigione, Alessandro; Garone, Caterina

Urinary Multi-Omics Profiling Reveals Systemic Molecular Alterations in Progressive External Ophthalmoplegia

尿液多组学分析揭示进行性眼外肌麻痹症的系统性分子改变

Cicchinelli, Michela; Primiano, Guido; Canu, Francesca; Gervasoni, Jacopo; Primiano, Aniello; Santucci, Lavinia; Percio, Anna; Greco, Viviana; Leoni, Chiara; Sabino, Andrea; Ardito, Michelangelo; Zampino, Giuseppe; Servidei, Serenella; Urbani, Andrea; Iavarone, Federica

Sudoscan in ATTRv Amyloidosis: A Potential Marker of Disease Progression?

Sudoscan在ATTRv淀粉样变性中的应用:疾病进展的潜在标志物?

Romano, Angela; Guglielmino, Valeria; Vitali, Francesca; Sciarrone, Maria Ausilia; Siconolfi, Giovanni; Di Paolantonio, Andrea; Primiano, Guido; Luigetti, Marco

Neurofilament Light Chain Levels as Diagnostic and Prognostic Biomarkers in Guillain-Barré Syndrome: An Updated Systematic Review and Meta-Analysis

神经丝轻链水平作为格林-巴利综合征的诊断和预后生物标志物:一项更新的系统评价和荟萃分析

Siconolfi, Giovanni; Vitali, Francesca; Sciarrone, Maria Ausilia; Guglielmino, Valeria; Primiano, Guido; Luigetti, Marco

Serum Biomarkers in Transthyretin Amyloidosis: An Overview of Neurofilaments, Cardiac, Renal, and Gastrointestinal Involvement

转甲状腺素蛋白淀粉样变性血清生物标志物:神经丝、心脏、肾脏和胃肠道受累概述

Guglielmino, Valeria; Vitali, Francesca; Romano, Angela; Primiano, Guido; Sciarrone, Maria Ausilia; Luigetti, Marco

Elevated serum concentrations of GFAP in hereditary transthyretin amyloidosis since pre-symptomatic stages

遗传性转甲状腺素蛋白淀粉样变性患者自症状出现前阶段起,血清中GFAP浓度即升高。

Plantone, Domenico; Luigetti, Marco; Manco, Carlo; Romano, Angela; Leonardi, Luca; Guglielmino, Valeria; Forcina, Francesca; Ceccanti, Marco; Inghilleri, Maurizio; Manganelli, Fiore; Tozza, Stefano; Sciarrone, Maria Ausilia; Vitali, Francesca; Sabino, Andrea; Righi, Delia; Stufano, Angela; Stromillo, Maria Laura; De Stefano, Nicola; Calabresi, Paolo; Primiano, Guido

Serum neuronal, glial and mitochondrial markers in autosomal dominant optic atrophy and Leber hereditary optic neuropathy

常染色体显性遗传性视神经萎缩和莱伯遗传性视神经病变患者的血清神经元、胶质细胞和线粒体标志物

Rufa, Alessandra; Plantone, Domenico; Bargagli, Alessia; Righi, Delia; Bacci, Tommaso; Serchi, Valeria; Primiano, Guido; Gallus, Gian Nicola; Lopergolo, Diego; Pretegiani, Elena; Rosini, Francesca; Locci, Sara; Tosi, Gian Marco; De Stefano, Nicola