2012
DOI: 10.1590/s0004-282x2012000100023
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Corrections

Abstract: In the paper: Sato Douglas, Fujihara Kazuo. Atypical presentations of neuromyelitis optica. Arq Neuro-Psiquiatr 2011; 69(5): 824-828, Table 1, the line: "Transient asymptomatic elevation of CK levels; observed few weeks prior to a NMO attack" must be placed in the thirth column, instead of the second column:

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“…Neuromyelitis optica (NMO) and neuromyelitis optica spectrum disorders (NMOSD) are a group of inflammatory disorders of the CNS characterized by immune-mediated demyelination and axonal damage, with primary target sites being the optic nerves and the spinal cord [1]. The usual presentation often involves sudden onset, severe episodes of optic neuritis and longitudinally extensive transverse myelitis [3]. The disease is most commonly associated with the presence of serum NMO-IgG antibodies that selectively bind aquaporin-4 (AQP4) and are highly disease specific [1].…”
Section: Discussionmentioning
confidence: 99%
“…Neuromyelitis optica (NMO) and neuromyelitis optica spectrum disorders (NMOSD) are a group of inflammatory disorders of the CNS characterized by immune-mediated demyelination and axonal damage, with primary target sites being the optic nerves and the spinal cord [1]. The usual presentation often involves sudden onset, severe episodes of optic neuritis and longitudinally extensive transverse myelitis [3]. The disease is most commonly associated with the presence of serum NMO-IgG antibodies that selectively bind aquaporin-4 (AQP4) and are highly disease specific [1].…”
Section: Discussionmentioning
confidence: 99%