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

Investigating the Frequency and Outcome of Central Vein Sign and Paramagnetic Rim Lesions in Children With MOGAD

探讨MOGAD患儿中心静脉征和顺磁性环状病变的发生频率和预后

Nistri, Riccardo; Cacciaguerra, Laura; Sacco, Simone; Virupakshaiah, Akash; De Meo, Ermelinda; Papinutto, Nico; Henry, Roland G; Meirson, Hadas; Hemingway, Cheryl; Rossor, Thomas; Wassmer, Evangeline; Bensira, Liat; Pratt, Li-Tal; Biswas, Asthik; Sudhakar, Sniya; Mankad, Kshitij; Chen, John J; Pittock, Sean J; Barkhof, Frederik; Ciccarelli, Olga; Waubant, Emmanuelle; Flanagan, Eoin P; Hacohen, Yael

Paramagnetic Rim Lesions in Pediatric Multiple Sclerosis and Their Association With Brain Tissue Atrophy

儿童多发性硬化症中的顺磁性环状病变及其与脑组织萎缩的关系

Nistri, Riccardo; De Meo, Ermelinda; Kim, Nee Na; Pozzilli, Valeria; Goebl, Philip; Sa, Mario; Ramdas, Sithara; Parida, Amitav; Wright, Sukhvir; Wassmer, Evangeline; Eyre, Michael; Lim, Ming; Rossor, Thomas; Hemingway, Cheryl; Biswas, Asthik; Sudhakar, Sniya; Mankad, Kshitij; Eshaghi, Arman; Barkhof, Frederik; Ciccarelli, Olga; Hacohen, Yael

Topological modelling of urban air pollution and cognition

城市空气污染与认知的拓扑建模

Engleitner, Holger; Suárez Pinilla, Marta; Rossor, Martin; Nachev, Parashkev

Slowly Expanding Lesions in Pediatric-Onset Multiple Sclerosis

儿童期发病的多发性硬化症中缓慢扩展的病灶

Pozzilli, Valeria; Prados Carrasco, Ferran; Kim, Neena; Abdel-Mannan, Omar; Nistri, Riccardo; Goebl, Philipp; Hemingway, Cheryl; Biswas, Asthik; Mankad, Kshitij; Sudhakar, Sniya; Parida, Amitav; Wright, Sukhvir; Wassmer, Evangeline; Eyre, Michael; Lim, Ming; Rossor, Thomas; Eshaghi, Arman; Barkhof, Frederik; De Meo, Ermelinda; Ciccarelli, Olga; Hacohen, Yael

Enabling new insights from old scans by repurposing clinical MRI archives for multiple sclerosis research

通过重新利用临床磁共振成像档案,从旧扫描中获得新的见解,用于多发性硬化症研究

Goebl, Philipp; Wingrove, Jed; Abdelmannan, Omar; Brito Vega, Barbara; Stutters, Jonathan; Ramos, Silvia Da Graca; Kenway, Owain; Rossor, Thomas; Wassmer, Evangeline; Arnold, Douglas L; Collins, D Louis; Hemingway, Cheryl; Narayanan, Sridar; Chataway, Jeremy; Chard, Declan; Iglesias, Juan Eugenio; Barkhof, Frederik; Parker, Geoff J M; Oxtoby, Neil P; Hacohen, Yael; Thompson, Alan; Alexander, Daniel C; Ciccarelli, Olga; Eshaghi, Arman

Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy

ARHGAP19基因的双等位基因变异会导致进行性遗传性运动为主的神经病。

Dominik, Natalia; Efthymiou, Stephanie; Record, Christopher J; Miao, Xinyu; Lin, Renee Q; Parmar, Jevin M; Scardamaglia, Annarita; Maroofian, Reza; Lowe, Simon A; Aughey, Gabriel N; Wilson, Abigail D; Curro, Riccardo; Schnekenberg, Ricardo P; Alavi, Shahryar; Leclaire, Leif; He, Yi; Zhelcheska, Kristina; Bellaïche, Yohanns; Gaugué, Isabelle; Skorupinska, Mariola; Van de Vondel, Liedewei; Da'as, Sahar I; Turchetti, Valentina; Güngör, Serdal; Monahan, Gavin V; Ghayoor Karimiani, Ehsan; Jamshidi, Yalda; Lamont, Phillipa J; Armirola-Ricaurte, Camila; Topaloglu, Haluk; Jordanova, Albena; Zaman, Mashaya; Banu, Selina H; Marques, Wilson; Tomaselli, Pedro J; Aynekin, Busra; Cansu, Ali; Per, Huseyin; Güleç, Ayten; Alvi, Javeria Raza; Sultan, Tipu; Khan, Arif; Zifarelli, Giovanni; Ibrahim, Shahnaz; Mancini, Grazia M S; Motazacker, M M; Brusse, Esther; Lupo, Vincenzo; Sevilla, Teresa; Başak, A Nazli; Tekgul, Seyma; Palvadeau, Robin J; Baets, Jonathan; Parman, Yesim; Çakar, Arman; Horvath, Rita; Haack, Tobias B; Stahl, Jan-Hendrik; Grundmann-Hauser, Kathrin; Park, Joohyun; Zuchner, Stephan; Laing, Nigel G; Wilson, Lindsay A; Rossor, Alexander M; Polke, James; Figueiredo, Fernanda Barbosa; Pessoa, André; Kok, Fernando; Coimbra-Neto, Antônio Rodrigues; Franca, Marcondes C Jr; Ravenscroft, Gianina; Hamed, Sherifa A; Chung, Wendy K; Pittman, Alan M; Osborn, Daniel P; Hanna, Michael; Cortese, Andrea; Reilly, Mary M; Jepson, James Ec; Lamarche-Vane, Nathalie; Houlden, Henry

Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD

由SORD基因突变引起的夏科-马里-图斯病的基因型和表型谱

Cortese, Andrea; Dohrn, Maike F; Curro, Riccardo; Negri, Sara; Lassuthova, Petra; Pisciotta, Chiara; Tozza, Stefano; Al-Ajmi, Abdullah; Feng, Changyong; Tomaselli, Pedro J; Fernandez-Eulate, Gorka; Haddad, Saif; Laurà, Matilde; Rossor, Alexander M; Vegezzi, Elisa; Facchini, Stefano; Sleigh, James N; Rebelo, Adriana; Beijer, Danique; Raposo, Jacquelyn; Saporta, Mario; Lauerova, Barbora; Pernice, Helena F; Achenbach, Pascal; Schöne, Ulrike; Alon, Tayir; Deschauer, Marcus; Cordts, Isabell; Obermaier, Carolin D; Winter, Natalie; Creigh, Peter D; Sowden, Janet E; Rehbein, Tyler; Magri, Stefania; Bertini, Alessandro; Saveri, Paola; Ripellino, Paolo; Huang, Jingyu; Nadaj-Pakleza, Aleksandra; Ross, Alison; Holt, James K L; Brennan, Kathryn M; Sukenik-Halevy, Rivka; Bizaoui, Varoona; Parman, Yesim; Battaloglu, Esra; Cakar, Arman; Alrohaif, Hadil; Hammans, Simon; Kumar, Kishore R; Kennerson, Marina L; Kayserili, Hülya; Amado, Defne A; Hahn, Katrin; Valentino, Paola; Cavalcanti, Francesca; Gaetano, Carlo; Taroni, Franco; Braathen, Geir J; Houlden, Henry; Stojkovic, Tanya; Peric, Stojan; Bolino, Alessandra; Previtali, Stefano C; Yi-Chung, Lee; Başak, Ayşe N; Hamed, Sherifa A; Rojas-Garcia, Ricardo; Claeys, Kristl G; Marques, Wilson; Sevilla, Teresa; Schlotter-Weigel, Beate; Manganelli, Fiore; Zhang, Ruxu; Herrmann, David N; Scherer, Steven S; Seeman, Pavel; Pareyson, Davide; Reilly, Mary M; Shy, Michael E; Züchner, Stephan

Perspectives on the diagnosis and management of functional cognitive disorder: An international Delphi study

关于功能性认知障碍的诊断和治疗的观点:一项国际德尔菲研究

Cabreira, Verónica; Alty, Jane; Antic, Sonja; Araújo, Rui; Aybek, Selma; Ball, Harriet A; Baslet, Gaston; Bhome, Rohan; Coebergh, Jan; Dubois, Bruno; Edwards, Mark; Filipović, Saša R; Frederiksen, Kristian Steen; Harbo, Thomas; Hayhow, Bradleigh; Howard, Robert; Huntley, Jonathan; Isaacs, Jeremy; LaFrance, William Curt Jr; Larner, Andrew J; Di Lorenzo, Francesco; Main, James; Mallam, Elizabeth; Marra, Camillo; Massano, João; McGrath, Emer R; McWhirter, Laura; Moreira, Isabel Portela; Nobili, Flavio; Pennington, Catherine; Tábuas-Pereira, Miguel; Perez, David L; Popkirov, Stoyan; Rayment, Dane; Rossor, Martin; Russo, Mirella; Santana, Isabel; Schott, Jonathan; Scott, Emmi P; Taipa, Ricardo; Tinazzi, Michele; Tomic, Svetlana; Toniolo, Sofia; Tørring, Caroline Winther; Wilkinson, Tim; Frostholm, Lisbeth; Stone, Jon; Carson, Alan

Understanding Mechanisms of Whole Brain and Regional Grey Matter Atrophy in Children With MOGAD

了解 MOGAD 患儿全脑和区域灰质萎缩的机制

De Meo, Ermelinda; Nistri, Riccardo; Eyre, Michael; Hemingway, Cheryl; Lim, Ming; Rossor, Thomas; Biswas, Asthik; Mankad, Kshitij; Siddiqui, Ata; Sudhakar, Sniya; Chard, Declan; Barkhof, Frederik; Eshaghi, Arman; Ciccarelli, Olga; Hacohen, Yael

Heterozygous PNPT1 Variants Cause a Sensory Ataxic Neuropathy

PNPT1杂合变异导致感觉性共济失调神经病

Haddad, Saif; Record, Christopher J; Self, Eleanor; Skorupinska, Mariola; Rossor, Alexander M; Laura, Matilde; Ingle, Gordon; Manzur, Adnan; Muntoni, Francesco; Blake, Julian C; Reilly, Mary M