期刊
MULTIPLE SCLEROSIS AND RELATED DISORDERS
卷 50, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.msard.2021.102852
关键词
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This report describes a case of a child with early and severe manifestations of AQP-4 positive NMOSD, who had refractory disease despite aggressive immunotherapy and ultimately underwent AHSCT.
We report on a child with an early and severe manifestation of an Aquaporin-4 (AQP-4) positive Neuromyelitis Optica Spectrum Disorder (NMOSD) who had a refractory disease course despite aggressive immunotherapy and underwent autologous hematopoietic stem cell transplant (AHSCT).
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