Latest Articles
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- ArticleGray matter–related proteins are associated with childhood-onset multiple sclerosisVaibhav Singh, E. Daniëlle van Pelt, Marcel P. Stoop, et al.September 24, 2015
- ArticleGRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitisGregory S. Day, Harald Prüss, Susanne M. Benseler, et al.September 24, 2015
- Clinical/Scientific NotesPediatric anti-Hu–associated encephalitis with clinical features of Rasmussen encephalitisBhooma R. Aravamuthan, Iván Sánchez Fernández, Jonathan Zurawski, et al.September 24, 2015
- Clinical/Scientific NotesIncomplete Susac syndrome exacerbated after natalizumabLana Zhovtis Ryerson, Ilya Kister, Matija Snuderl, et al.September 24, 2015
- Clinical/Scientific NotesPlasticity-related gene 5: A novel surface autoantigen in paraneoplastic cerebellar degenerationMarleen H. van Coevorden-Hameete, Esther de Graaff, Maarten J. Titulaer, et al.September 24, 2015
- ArticlePharmacogenomic study in patients with multiple sclerosisResponders and nonresponders to IFN-βMarta F. Bustamante, Carlos Morcillo-Suárez, Sunny Malhotra, et al.September 24, 2015
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Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
Dr. Robert Pitceathly and Dr. William Macken