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

Metronome-guided training accelerates the adaptation to an aerobic training pace in swimming

节拍器引导训练可以加快游泳运动员对有氧训练节奏的适应。

Fassone, Marco; Puce, Luca; Biggio, Monica; Avanzino, Laura; Bove, Marco; Bisio, Ambra

Muscle Fatigue and Swimming Efficiency in Behind and Lateral Drafting

肌肉疲劳与后方和侧向跟游时的游泳效率

Puce, Luca; Chamari, Karim; Marinelli, Lucio; Mori, Laura; Bove, Marco; Faelli, Emanuela; Fassone, Marco; Cotellessa, Filippo; Bragazzi, Nicola Luigi; Trompetto, Carlo

Expanding the phenotypic spectrum of BCS1L-related mitochondrial disease

扩大BCS1L相关线粒体疾病的表型谱

Hikmat, Omar; Isohanni, Pirjo; Keshavan, Nandaki; Ferla, Matteo P; Fassone, Elisa; Abbott, Mary-Alice; Bellusci, Marcello; Darin, Niklas; Dimmock, David; Ghezzi, Daniele; Houlden, Henry; Invernizzi, Federica; Kamarus Jaman, Nazreen B; Kurian, Manju A; Morava, Eva; Naess, Karin; Ortigoza-Escobar, Juan Darío; Parikh, Sumit; Pennisi, Alessandra; Barcia, Giulia; Tylleskär, Karin B; Brackman, Damien; Wortmann, Saskia B; Taylor, Jenny C; Bindoff, Laurence A; Fellman, Vineta; Rahman, Shamima

Quality of Life in Electrochemotherapy for Cutaneous and Mucosal Head and Neck Tumors

电化学疗法治疗头颈部皮肤和黏膜肿瘤的生活质量

Riva, Giuseppe; Salonia, Laura; Fassone, Elisabetta; Sapino, Silvia; Piano, Fabrizio; Pecorari, Giancarlo

Head and neck cancer surgery in COVID-19 pandemic in Northern Italy

意大利北部新冠疫情期间的头颈癌手术

Riva, Giuseppe; Pizzo, Claudia; Fassone, Elisabetta; Pecorari, Giancarlo

The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndrome

癸酸处理对复合体I缺陷型莱氏综合征患者成纤维细胞线粒体功能的多效性影响

Kanabus, Marta; Fassone, Elisa; Hughes, Sean David; Bilooei, Sara Farahi; Rutherford, Tricia; Donnell, Maura O'; Heales, Simon J R; Rahman, Shamima

TRNT1 deficiency: clinical, biochemical and molecular genetic features

TRNT1 缺乏症:临床、生化和分子遗传学特征

Wedatilake, Yehani; Niazi, Rojeen; Fassone, Elisa; Powell, Christopher A; Pearce, Sarah; Plagnol, Vincent; Saldanha, José W; Kleta, Robert; Chong, W Kling; Footitt, Emma; Mills, Philippa B; Taanman, Jan-Willem; Minczuk, Michal; Clayton, Peter T; Rahman, Shamima

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

FOXRED1 编码一种 FAD 依赖性氧化还原酶复合物 I 特异性分子伴侣,其突变与婴儿期发病的线粒体脑病有关。

Fassone, Elisa; Duncan, Andrew J; Taanman, Jan-Willem; Pagnamenta, Alistair T; Sadowski, Michael I; Holand, Tatjana; Qasim, Waseem; Rutland, Paul; Calvo, Sarah E; Mootha, Vamsi K; Bitner-Glindzicz, Maria; Rahman, Shamima

Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability

DNA2基因突变将进行性肌病与线粒体DNA不稳定性联系起来

Ronchi, Dario; Di Fonzo, Alessio; Lin, Weiqiang; Bordoni, Andreina; Liu, Changwei; Fassone, Elisa; Pagliarani, Serena; Rizzuti, Mafalda; Zheng, Li; Filosto, Massimiliano; Ferrò, Maria Teresa; Ranieri, Michela; Magri, Francesca; Peverelli, Lorenzo; Li, Hongzhi; Yuan, Yate-Ching; Corti, Stefania; Sciacco, Monica; Moggio, Maurizio; Bresolin, Nereo; Shen, Binghui; Comi, Giacomo Pietro

The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment

线粒体tRNAAsn基因m.5709T>C突变是一种新型突变,可导致眼肌麻痹和呼吸功能障碍。

Ronchi, Dario; Sciacco, Monica; Bordoni, Andreina; Raimondi, Monika; Ripolone, Michela; Fassone, Elisa; Di Fonzo, Alessio; Rizzuti, Mafalda; Ciscato, Patrizia; Cosi, Alessandra; Servida, Maura; Moggio, Maurizio; Corti, Stefania; Bresolin, Nereo; Comi, Giacomo P