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

Phospholipid-driven conformational switching of HCV NS5A links protein folding to replication membrane remodeling

磷脂驱动的HCV NS5A构象转换将蛋白质折叠与复制膜重塑联系起来

Bulankina, Anna V; Richter, Rebecca M; Nettles, James H; Yamane, Daisuke; Grimm, Christian; Karami, Yasaman; Stanton, Richard A; Introini, Bianca; Hermann, Jonas; Charif, Hanaa; König, Mia S; Stroß, Claudia; Ortiz, Cristina; Kraus, Nico; Wood, Daniel; Galceran, Facundo; Abele, Rupert; Maigret, Bernard; Schinazi, Raymond F; Zeuzem, Stefan; Biondi, Ricardo M; Yi, MinKyung; Tampé, Robert; Kudryashev, Mikhail; Welsch, Christoph

Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic Atrophy

ACO2相关显性视神经萎缩的临床和遗传谱

Beaulieu, Cléis; Bouzidi, Aymane; Desquiret-Dumas, Valérie; Dieu, Xavier; Makam, Rahul; Jurkute, Neringa; Vignal, Catherine; Philibert, Manon; Odent, Sylvie; Zanlonghi, Xavier; Latypov, Marie; Debourdeau, Eloi; Bocquet, Béatrice; Yahia, Raihane; Pons, Linda; Villard, Frédéric Pollet; Jeanjean, Luc; Verrecchia, Sarah; Froment, Caroline; Engel, Camille; Poirsier, Céline; Arndt, Carl; Dollfus, Hélène; Gohier, Philippe; Charif, Majida; Ferré, Marc; Prunier-Mirebeau, Delphine; Meunier, Isabelle; Yu-Wai-Man, Patrick; Amati-Bonneau, Patrizia; Lenaers, Guy; Smirnov, Vasily

Effect on Dyskinesia of the Early Combination of Amantadine to Levodopa-Therapy in Parkinson's Disease: A Randomized, Placebo-Controlled Study (PREMANDYSK)

金刚烷胺与左旋多巴早期联合治疗对帕金森病运动障碍的影响:一项随机、安慰剂对照研究(PREMANDYSK)

Rascol, Olivier; Ory-Magne, Fabienne; Meissner, Wassilios G; Maltête, David; Defebvre, Luc; Azulay, Jean-Philippe; Thobois, Stéphane; Houeto, Jean-Luc; Thalamas, Claire; Sommet, Agnès; Geny, Christian; Damier, Philippe; Anheim, Mathieu; Marquès, Ana; Viallet, François; Giroud, Maurice; Lefaucheur, Romain; Costentin, Guillaume; Spampinato, Umberto; Samier-Foubert, Alexandra; Carrière, Nicolas; Mutez, Eugénie; Mariani, Louise-Laure; Eusebio, Alexandre; Prange, Stéphane; Benatru, Isabelle; Charif, Mahmoud; Brefel-Courbon, Christine; Fabbri, Margherita; Galitzky, Monique; Rousseau, Vanessa; Saubion, Amandine; Catala, Hélène; Ferreira, Joaquim J; Burn, David J; Corvol, Jean-Christophe

Bevacizumab withdrawal–associated cortical hyperperfusion in recurrent high-grade astrocytoma: An underrecognized MRI pitfall

贝伐单抗停药相关复发性高级别星形细胞瘤皮质高灌注:一个未被充分认识的MRI陷阱

Sriwastwa, Aakanksha; Oswald, Michael K; Vagal, Achala S; Demel, Stacie L; Zhang, Bin; Voleti, Sriharsha; Ali, Arafat; Morgan, Daniel; Thompson, Trevor; Vidovich, Johnathan; Aziz, Yasmin N; Wang, Lily Li-Li; Coelho, Alice; Chen, Zhijian; Sidani, Charif; Abrams, Kevin J; Freitas, Leonardo Furtado

Validation of the French Translation of the Movement Disorder Society Non-Motor Symptoms Scale (MDS-NMS) in Parkinson's Disease

帕金森病运动障碍协会非运动症状量表(MDS-NMS)法语版的验证

Desjardins, Clément; Grimaldi, Stéphan; Luo, Sheng; Yu, Luowen; Goetz, Christopher G; Stebbins, Glenn T; Martinez-Martin, Pablo; Kurtis, Monica M; Mestre, Tiago A; Sanchez-Ferro, Alvaro; Tosin, Michelle H S; Balestrino, Roberta; Lin, Chi-Ying R; Gasca-Salas, Carmen; Witjas, Tatiana; Colin, Olivier; Maltete, David; Defebvre, Luc; Giordana, Caroline; Charif, Mahmoud; Thiriez, Claire; Laurencin, Chloé; Tir, Mélissa; Dupont, Gwendoline; Remy, Philippe; Tranchant, Christine; Drapier, Sophie; Samier, Alexandra; Benatru, Isabelle; Sambin, Sara; Corvol, Jean-Christophe; Khelifi, Fatma; Fabbri, Margherita; Rascol, Olivier

A rare case of subclavian steal phenomenon: when a dialysis arm arteriovenous fistula robs the brain

锁骨下静脉盗血现象罕见病例:透析臂动静脉瘘窃取脑血

Freitas, Leonardo Furtado; Hodges, Tate; Sidani, Charif; Abrams, Kevin J

Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic Diagnosis

北非生物样本库中遗传性疾病致病基因的鉴定:对基因诊断的启示

Charif, Majida; Lhousni, Saida; Ghanam, Ayad; Rkain, Maria; Benajiba, Noufissa; Amrani, Rim; Babakhouya, Abdeladim; Messaoudi, Sahar; Elouali, Aziza; Ayyad, Anass; Najib, Abdeljaouad; El Mahi, Omar; Benzirar, Adnane; Moutaouekkil, Mehdi; Allaoui, Sanae; Benahmed, Mohammed; Elidrissi Errahhali, Manal; Elidrissi Errahhali, Mounia; Bouzidi, Aymane; Ouarzane, Meryem; Vincent, Antony T; Sellam, Adnane; Lenaers, Guy; Boulouiz, Redouane; Bellaoui, Mohammed

Incidental finding of "H"-type duplex gallbladder: a case report

偶然发现“H”型重复胆囊:病例报告

Chami Khazraji, Idriss; El Houari, Zainab; Charif Saibari, Rayhana; Bennani, Samia; El Hattab, Meryem; Bouknani, Nawal; Rami, Amal

Corrigendum to Multiomic analysis in fibroblasts of patients with inborn errors of cobalamin metabolism reveals concordance with clinical and metabolic variability [eBioMedicine 99 (2024), 104911]

对患有先天性钴胺素代谢异常患者的成纤维细胞多组学分析揭示了与临床和代谢变异性的一致性[eBioMedicine 99 (2024), 104911]的更正

Wiedemann, Arnaud; Oussalah, Abderrahim; Guéant Rodriguez, Rosa-Maria; Jeannesson, Elise; Merten, Marc; Rotaru, Irina; Alberto, Jean-Marc; Baspinar, Okan; Rashka, Charif; Hassan, Ziad; Siblini, Youssef; Matmat, Karim; Jeandel, Manon; Chery, Celine; Robert, Aurélie; Chevreux, Guillaume; Lignières, Laurent; Camadro, Jean-Michel; Feillet, François; Coelho, David; Guéant, Jean-Louis

Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment

NDUFA13双等位基因变异会导致神经发育表型,并伴有逐渐加重的神经功能障碍。

Kaiyrzhanov, Rauan; Thompson, Kyle; Efthymiou, Stephanie; Mukushev, Askhat; Zharylkassyn, Akbota; Prasad, Chitra; Ghayoor Karimiani, Ehsan; Alvi, Javeria Raza; Niyazov, Dmitriy; Alahmad, Ahmad; Babaei, Meisam; Tajsharghi, Homa; Albash, Buthaina; Alaqeel, Ahmad; Charif, Majida; Hashemi, Narges; Heidari, Morteza; Kalantar, Seyed Mehdi; Lenaers, Guy; Vahidi Mehrjardi, Mohammad Yahya; Srinivasan, Varunvenkat M; Gowda, Vykuntaraju K; Mirabutalebi, Seyed Hamidreza; Carere, Deanna Alexis; Movahedinia, Mojtaba; Murphy, David; McFarland, Robert; Abdel-Hamid, Mohamed S; Elhossini, Rasha M; Alavi, Shahryar; Napier, Melanie; Belanger-Quintana, Amaya; Prasad, Asuri N; Jakobczyk, Jessica; Roubertie, Agathe; Rupar, Tony; Sultan, Tipu; Toosi, Mehran Beiraghi; Sazanov, Leonid; Severino, Mariasavina; Houlden, Henry; Taylor, Robert W; Maroofian, Reza