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MOG antibody-associated encephalomyelitis/encephalitis.
Mult Scler. 2019 10; 25(11):1427-1433.MS

Abstract

Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a rare autoimmune disorder with antibodies against the MOG predominantly involving the optic nerve and spinal cord leading to vision loss and paralysis. When MOG antibody disease involves the brain, the phenotype is similar to acute disseminated encephalomyelitis (ADEM). In this review, we discuss MOG-positive cases presenting with encephalitis, encephalopathy, or ADEM-like presentation based on recently published series.

Authors+Show Affiliations

Department of Neurology, Johns Hopkins University, Baltimore, MD, USA/Department of Neurology, University of Alexandria, Alexandria, Egypt.Department of Neuroradiology, Johns Hopkins University, Baltimore, MD, USA.Department of Neurology,Johns Hopkins University,Baltimore, MD,USA.Department of Neuroradiology, Johns Hopkins University, Baltimore, MD, USA.Department of Neurology, Johns Hopkins University, Baltimore, MD, USA/Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review

Language

eng

PubMed ID

30907249

Citation

Salama, Sara, et al. "MOG Antibody-associated Encephalomyelitis/encephalitis." Multiple Sclerosis (Houndmills, Basingstoke, England), vol. 25, no. 11, 2019, pp. 1427-1433.
Salama S, Khan M, Pardo S, et al. MOG antibody-associated encephalomyelitis/encephalitis. Mult Scler. 2019;25(11):1427-1433.
Salama, S., Khan, M., Pardo, S., Izbudak, I., & Levy, M. (2019). MOG antibody-associated encephalomyelitis/encephalitis. Multiple Sclerosis (Houndmills, Basingstoke, England), 25(11), 1427-1433. https://doi.org/10.1177/1352458519837705
Salama S, et al. MOG Antibody-associated Encephalomyelitis/encephalitis. Mult Scler. 2019;25(11):1427-1433. PubMed PMID: 30907249.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - MOG antibody-associated encephalomyelitis/encephalitis. AU - Salama,Sara, AU - Khan,Majid, AU - Pardo,Santiago, AU - Izbudak,Izlem, AU - Levy,Michael, Y1 - 2019/03/25/ PY - 2019/3/26/pubmed PY - 2020/6/23/medline PY - 2019/3/26/entrez KW - MOG antibody disease KW - MOG encephalomyelitis KW - MOG-EM KW - anti-MOG KW - myelin oligodendrocyte glycoprotein KW - optic neuritis KW - transverse myelitis SP - 1427 EP - 1433 JF - Multiple sclerosis (Houndmills, Basingstoke, England) JO - Mult Scler VL - 25 IS - 11 N2 - Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a rare autoimmune disorder with antibodies against the MOG predominantly involving the optic nerve and spinal cord leading to vision loss and paralysis. When MOG antibody disease involves the brain, the phenotype is similar to acute disseminated encephalomyelitis (ADEM). In this review, we discuss MOG-positive cases presenting with encephalitis, encephalopathy, or ADEM-like presentation based on recently published series. SN - 1477-0970 UR - https://www.unboundmedicine.com/medline/citation/30907249/MOG_antibody_associated_encephalomyelitis/encephalitis_ L2 - https://journals.sagepub.com/doi/10.1177/1352458519837705?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -