Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
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Myelin Oligodendrocyte Glycoprotein: Deciphering a Target in Inflammatory Demyelinating Diseases.MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 1: Frequency, syndrome specificity, influence of disease activity, long-term course, association with AQP4-IgG, and origin.Anti-myelin oligodendrocyte glycoprotein antibodies: Magnetic resonance imaging findings in a case series and a literature review.Clinical spectrum and IgG subclass analysis of anti-myelin oligodendrocyte glycoprotein antibody-associated syndromes: a multicenter study.Immunopathogenesis in Myasthenia Gravis and Neuromyelitis Optica.Emerging Role of Immunity in Cerebral Small Vessel Disease.MOG-IgG-Associated Optic Neuritis, Encephalitis, and Myelitis: Lessons Learned From Neuromyelitis Optica Spectrum Disorder.
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Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 26 February 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
@en
Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
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label
Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
@en
Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
@nl
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Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
@en
Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
@nl
P2093
P2860
P1476
Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD.
@en
P2093
Aimee Borazanci
Fu-Dong Shi
Jeffrey L Bennett
Kaibin Shi
Timothy L Vollmer
P2860
P2888
P304
P356
10.1007/S11427-015-4997-Y
P577
2016-02-26T00:00:00Z