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Get Free AccessA primary goal is to ensure high-quality evidence-based treatment for children and adolescents with MS, which will improve our understanding of the safety of these agents and remove regulatory or insurance-based limitations in access to treatment.
Emmanuelle Waubant, Brenda Banwell, Evangeline Wassmer, Maria Pia Sormani, Maria Pia Amato, Rogier Hintzen, Lauren Krupp, Kevin Rostásy, Sílvia Tenembaum, Tanuja Chitnis, Gregory Aaen, Elhachmia Ait Ben Adou, Raed Alroughani, Veronica Gonzalez Alvarez, Maria Anagnostouli, Banu Anlar, Thaís Armangué, Georgina Arrambide, Damiano Baroncini, R Ts Bembeeva, Leslie Benson, Neli Bizjak, Astrid Blaschek, Alexey Boyко, J. Nicholas Brenton, Wolfgang Brück, Bruna Klein da Costa, Dominique Dive, Christiane Elpers, Massimo Filippi, Manuela de Oliveira Fragomeni, Eva Havrdová, Cheryl Hemingway, Barbara Kornek, Kumaran Deiva, Adrian R. Lacy, Zuzana Libá, Ming Lim, Tim Lotze, Jean K. Mah, Naila Makhani, Soe Mar, Kyla A. McKay, Shay Menascu, Lucia Moiola, Patricia Mulero, Moustapha Ndiaye, Rinze F. Neuteboom, Jayne Ness, Enedina Maria Lobato de Oliveira, Scott Otallah, Francesco Patti, José Albino da Paz, Carlos A. Pérez, Daniela Pohl, Anne‐Louise Ponsonby, Mary Rensel, Maria A. Rocca, Nick Rijke, Moses Rodriguez, Ian Rossman, Hiroshi Sakuma, Teri Schreiner, Ángeles Schteinschnaider, E. Morghen Sikes, Isabella Laura Simone, Michael Sweeney, Jan Mendelt Tillema, Regina M. Troxell, Hélène Verhelst, Leidi Vilchez, Liesbeth De Waele, Bianca Weinstock‐Guttman, Colin Wilbur, Mikaeloff Yann, E. Ann Yeh, Dimitrios Zafeiriou (2019). Clinical trials of disease-modifying agents in pediatric MS. , 92(22), DOI: https://doi.org/10.1212/wnl.0000000000007572.
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Type
Article
Year
2019
Authors
77
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1212/wnl.0000000000007572
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