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American Journal of Human Genetics|July 3, 2021
Targeted long-read sequencing identifies missing disease-causing variationDanny E Miller, Arvis Sulovari, Tianyun Wang, et al.Neurology(R) Neuroimmunology & Neuroinflammation|August 4, 2015
Update on biomarkers in neuromyelitis opticaEsther Melamed, Michael Levy, Patrick J Waters, et al.Multiple Sclerosis and Related Disorders|July 7, 2020
Treatment of MOG-IgG-associated disorder with rituximab: An international study of 121 patientsDaniel H Whittam, Alvaro Cobo-Calvo, A Sebastian Lopez-Chiriboga, et al.Proceedings of the National Academy of Sciences of the United States of America|February 2, 2021
Cytoplasmic synthesis of endogenous Alu complementary DNA via reverse transcription and implications in age-related macular degenerationShinichi Fukuda, Akhil Varshney, Benjamin J Fowler, et al.JAMA Neurology|July 13, 2026
Interleukin 6 Receptor Blockade for Relapse Prevention in Myelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseAndreu Vilaseca, Philippe A Bilodeau, Georgios Gakis, et al.Journal of Neurology|July 6, 2020
Treatment of MOG antibody associated disorders: results of an international surveyD H Whittam, V Karthikeayan, E Gibbons, et al.Genome Biology|August 19, 2007
A physical map of the bovine genomeWarren M Snelling, Readman Chiu, Jacqueline E Schein, et al.Neurology(R) Neuroimmunology & Neuroinflammation|July 30, 2019
Collaborative International Research in Clinical and Longitudinal Experience Study in NMOSDLawrence J Cook, John W Rose, Jessica S Alvey, et al.Nature|June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.Brain : a Journal of Neurology|September 28, 2023
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.Pageof 267