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Serial anti–myelin oligodendrocyte glycoprotein antibody analyses and outcomes in children with demyelinating syndromes

Abstract:

Importance Identifying the course of demyelinating disease associated with myelin oligodendrocyte glycoprotein (MOG) autoantibodies is critical to guide appropriate treatment choices.

Objective To characterize serial anti-MOG antibody serologies and clinical and imaging features at presentation and during follow-up in an inception cohort of prospectively monitored children with acquired demyelination.

Design, Setting, and Particip...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1001/jamaneurol.2019.2940

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
ORCID:
0000-0003-4142-2667
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
et al.
Publisher:
American Medical Association
Journal:
JAMA Neurology More from this journal
Volume:
77
Issue:
1
Pages:
82-93
Publication date:
2019-09-23
Acceptance date:
2019-06-21
DOI:
EISSN:
2168-6157
ISSN:
2168-6149
Language:
English
Keywords:
Pubs id:
pubs:1020872
UUID:
uuid:215c5f4a-f681-4934-9b5b-d656bcd345ec
Local pid:
pubs:1020872
Source identifiers:
1020872
Deposit date:
2019-06-24

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