Publisher Full Text
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.
Links
MeSH
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 -