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

Epstein-Barr Virus Antibodies to Differentiate Multiple Sclerosis From Other Neuroinflammatory Diseases

利用 Epstein-Barr 病毒抗体鉴别多发性硬化症与其他神经炎症性疾病

Vietzen, Hannes; Kühner, Laura M; Berger, Sarah M; Reinecke, Raphael; Rostásy, Kevin; Saucke, Henrieke; Kauth, Franziska; Koukou, Georgia; Sommer, Simon; Wendel, Eva-Maria; Graninger, Marianne; Camp, Jeremy V; Waubant, Emmanuelle L; Casper, T Charles; Benson, Leslie A; Chitnis, Tanuja; Aaen, Gregory S; Mar, Soe; Weinstock-Guttman, Bianca; Lotze, Timothy E; Krupp, Lauren B; Lassmann, Hans; Weidner, Lisa; Pistorius, Charlotte; Jungbauer, Christof; Ponleitner, Markus; Reindl, Markus; Kornek, Barbara; Breu, Markus; Bsteh, Gabriel; Höftberger, Romana; Berger, Thomas; Puchhammer-Stöckl, Elisabeth; Rommer, Paulus

Real-World Effectiveness of Switching to Oral or Infusion Versus Injectable Disease-Modifying Therapy in Pediatric Multiple Sclerosis

儿童多发性硬化症中,改用口服或输注疗法与注射疗法相比的实际疗效

Abrams, Aaron W; Waltz, Michael; Casper, T Charles; Aaen, Gregory; Benson, Leslie A; Bernfeld, Eva-Chava M; Charvet, Leigh E; Chitnis, Tanuja; Francisco, Carla; Gorman, Mark P; Graves, Jennifer S; Krupp, Lauren; O'Neill, Kimberly; Lotze, Timothy E; Mar, Soe; Ness, Jayne; Rensel, Mary; Rodriguez, Moses; Rose, John; Rutatangwa, Alice; Schreiner, Teri; Shukla, Nikita; Tillema, Jan-Mendelt; Weinstock-Guttman, Bianca; Wheeler, Yolanda; Waubant, Emmanuelle; Krysko, Kristen M

Epigenetic Aging in Pediatric-Onset Multiple Sclerosis

儿童期发病的多发性硬化症中的表观遗传衰老

Goyne, Christopher; Fair, Ashley E; Yilmaz, Defne; Race, Jonathan; Schuette, Allison; Caillier, Stacy J; Aaen, Gregory S; Abrams, Aaron W; Benson, Leslie A; Casper, T Charles; Chitnis, Tanuja; Gorman, Mark P; Lotze, Timothy E; Krupp, Lauren B; Mar, Soe S; Ness, Jayne M; Rensel, Mary; Rodriguez, Moses; Rose, John W; Schreiner, Teri L; Tillema, Jan-Mendelt; Waldman, Amy Tara; Wheeler, Yolanda S; Barcellos, Lisa F; Waubant, Emmanuelle; Graves, Jennifer S

Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variants.

由双等位基因 COL12A1 变异引起的 XII 型胶原蛋白相关疾病的临床特征

McCarty Riley M, Saade Dimah, Munot Pinki, Laverty Chamindra G, Pinz Hailey, Zou Yaqun, McAnally Meghan, Yun Pomi, Tian Cuixia, Hu Ying, Feng Lucy, Phadke Rahul, Ceulemans Sophia, Magoulas Pilar, Skalsky Andrew J, Friedman Jennifer R, Braddock Stephen R, Neuhaus Sarah B, Malicki Denise M, Bainbridge Matthew N, Nahas Shareef, Dimmock David P, Kingsmore Stephen F, Lotze Timothy E, Foley A Reghan, Muntoni Francesco, Straub Volker, Donkervoort Sandra, Bönnemann Carsten G

Early Adversity and Socioeconomic Factors in Pediatric Multiple Sclerosis: A Case-Control Study

儿童多发性硬化症早期逆境和社会经济因素:一项病例对照研究

Jensen, Sarah K G; Camposano, Susana; Berens, Anne; Waltz, Michael; Krupp, Lauren B; Charvet, Leigh; Belman, Anita L; Aaen, Gregory S; Benson, Leslie A; Candee, Meghan; Casper, Theron C; Chitnis, Tanuja; Graves, Jennifer; Wheeler, Yolanda S; Kahn, Ilana; Lotze, Timothy E; Mar, Soe S; Rensel, Mary; Rodriguez, Moses; Rose, John W; Rubin, Jennifer P; Tillema, Jan-Mendelt; Waldman, Amy T; Weinstock-Guttman, Bianca; Barcellos, Lisa F; Waubant, Emmanuelle; Gorman, Mark P

Predictors of a relapsing course in myelin oligodendrocyte glycoprotein antibody-associated disease

髓鞘少突胶质细胞糖蛋白抗体相关疾病复发病程的预测因素

Virupakshaiah, Akash; Schoeps, Vinicius A; Race, Jonathan; Waltz, Michael; Sharayah, Siefaddeen; Nasr, Zahra; Moseley, Carson E; Zamvil, Scott S; Gaudioso, Cristina; Schuette, Allison; Casper, Theron Charles; Rose, John; Flanagan, Eoin P; Rodriguez, Moses; Tillema, Jan-Mendelt; Chitnis, Tanuja; Gorman, Mark P; Graves, Jennifer S; Benson, Leslie A; Rensel, Mary; Abrams, Aaron; Krupp, Lauren; Lotze, Timothy E; Aaen, Gregory; Wheeler, Yolanda; Schreiner, Teri; Waldman, Amy; Chong, Janet; Mar, Soe; Waubant, Emmanuelle

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

胆碱和乙醇胺转运蛋白FLVCR1的双等位基因变异是多种疾病谱的基础,涵盖从成人神经退行性疾病到严重发育障碍。

Calame, Daniel G; Wong, Jovi Huixin; Panda, Puravi; Nguyen, Dat Tuan; Leong, Nancy C P; Sangermano, Riccardo; Patankar, Sohil G; Abdel-Hamid, Mohamed; AlAbdi, Lama; Safwat, Sylvia; Flannery, Kyle P; Dardas, Zain; Fatih, Jawid M; Murali, Chaya; Kannan, Varun; Lotze, Timothy E; Herman, Isabella; Ammouri, Farah; Rezich, Brianna; Efthymiou, Stephanie; Alavi, Shahryar; Murphy, David; Firoozfar, Zahra; Nasab, Mahya Ebrahimi; Bahreini, Amir; Ghasemi, Majid; Haridy, Nourelhoda A; Goldouzi, Hamid Reza; Eghbal, Fatemeh; Karimiani, Ehsan Ghayoor; Srinivasan, Varunvenkat M; Gowda, Vykuntaraju K; Du, Haowei; Jhangiani, Shalini N; Coban-Akdemir, Zeynep; Marafi, Dana; Rodan, Lance; Isikay, Sedat; Rosenfeld, Jill A; Ramanathan, Subhadra; Staton, Michael; Kerby C Oberg; Clark, Robin D; Wenman, Catharina; Loughlin, Sam; Saad, Ramy; Ashraf, Tazeen; Male, Alison; Tadros, Shereen; Boostani, Reza; Abdel-Salam, Ghada M H; Zaki, Maha; Abdalla, Ebtesam; Manzini, M Chiara; Pehlivan, Davut; Posey, Jennifer E; Gibbs, Richard A; Houlden, Henry; Alkuraya, Fowzan S; Bujakowska, Kinga; Maroofian, Reza; Lupski, James R; Nguyen, Long Nam

Therapeutic Response in Pediatric Neuromyelitis Optica Spectrum Disorder

儿童视神经脊髓炎谱系障碍的治疗反应

Pizzolato Umeton, Raffaella; Waltz, Michael; Aaen, Gregory S; Benson, Leslie; Gorman, Mark; Goyal, Manu; Graves, Jennifer S; Harris, Yolanda; Krupp, Lauren; Lotze, Timothy E; Shukla, Nikita M; Mar, Soe; Ness, Jayne; Rensel, Mary; Schreiner, Teri; Tillema, Jan-Mendelt; Roalstad, Shelly; Rodriguez, Moses; Rose, John; Waubant, Emmanuelle; Weinstock-Guttman, Bianca; Casper, Charles; Chitnis, Tanuja

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

HMGCR基因的双等位基因变异会导致常染色体隐性遗传的进行性肢带型肌营养不良症。

Morales-Rosado, Joel A; Schwab, Tanya L; Macklin-Mantia, Sarah K; Foley, A Reghan; Pinto E Vairo, Filippo; Pehlivan, Davut; Donkervoort, Sandra; Rosenfeld, Jill A; Boyum, Grace E; Hu, Ying; Cong, Anh T Q; Lotze, Timothy E; Mohila, Carrie A; Saade, Dimah; Bharucha-Goebel, Diana; Chao, Katherine R; Grunseich, Christopher; Bruels, Christine C; Littel, Hannah R; Estrella, Elicia A; Pais, Lynn; Kang, Peter B; Zimmermann, Michael T; Lupski, James R; Lee, Brendan; Schellenberg, Matthew J; Clark, Karl J; Wierenga, Klaas J; Bönnemann, Carsten G; Klee, Eric W

Familial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis

儿童多发性硬化症患者的自身免疫性疾病家族史

Greenberg, Benjamin M; Casper, Theron Charles; Mar, Soe S; Ness, Jayne M; Plumb, Patricia; Liang, Shannon; Goyal, Manu; Weinstock-Guttman, Bianca; Rodriguez, Moses; Aaen, Gregory S; Belman, Anita; Barcellos, Lisa F; Rose, John W; Gorman, Mark P; Benson, Leslie A; Candee, Meghan; Chitnis, Tanuja; Harris, Yolanda C; Kahn, Ilana L; Roalstad, Shelly; Hart, Janace; Lotze, Timothy E; Rensel, Mary; Rubin, Jennifer P; Schreiner, Teri L; Tillema, Jan-Mendelt; Waldman, Amy Tara; Krupp, Lauren; Graves, Jennifer; Drake, Kaylea; Waubant, Emmanuelle