Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
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Contrasting disease patterns in seropositive and seronegative neuromyelitis optica: A multicentre study of 175 patientsInternational consensus diagnostic criteria for neuromyelitis optica spectrum disordersConventional and advanced imaging in neuromyelitis opticaMRI characteristics of neuromyelitis optica spectrum disorder: an international updateThe expanded spectrum of neuromyelitis optica: evidences for a new definition.Clinical spectrum and treatment of neuromyelitis optica spectrum disorders: evolution and current status.Neuromyelitis optica - an update: 2007-2009Recurrent Longitudinally Extensive Myelitis and Aquaporin-4 Seronegativity - The Expanding Spectrum of Neuromyelitis Optica.Differential diagnosis of neuromyelitis optica spectrum disorders.Conventional brain MRI in neuromyelitis optica.A longitudinal brain magnetic resonance imaging study of neuromyelitis optica spectrum disorderAQP4 autoantibody assay performance in clinical laboratory service.The pathology of an autoimmune astrocytopathy: lessons learned from neuromyelitis optica.Update on the diagnosis and treatment of neuromyelitis optica: recommendations of the Neuromyelitis Optica Study Group (NEMOS).Diagnostic utility of aquaporin-4 in the analysis of active demyelinating lesions.Brain abnormalities in neuromyelitis optica spectrum disorder.Magnetic resonance imaging brain findings in a case of aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder, presenting with intractable vomiting and hiccups.EFNS guidelines on diagnosis and management of neuromyelitis optica.Neuromyelitis optica with linear enhancement of corpus callosum in brain magnetic resonance imaging with contrast: a case report.Periventricular lesions help differentiate neuromyelitis optica spectrum disorders from multiple sclerosis.NMO-DBr: the Brazilian Neuromyelitis Optica Database System.Characteristic brain magnetic resonance imaging abnormalities in central nervous system aquaporin-4 autoimmunity.Diffuse and heterogeneous T2-hyperintense lesions in the splenium are characteristic of neuromyelitis optica.Cortical and leptomeningeal involvement in three cases of neuromyelitis optica.Cognitive function, depression, fatigue, and activities of daily living in patients with neuromyelitis optica after acute relapse.Diagnostik und Therapie der Neuromyelitis opticaNeuromyelitis optica should be classified as an astrocytopathic disease rather than a demyelinating diseaseDiagonistic Apraxia: A Unique Case of Corpus Callosal Disconnection Syndrome and Neuromyelitis Optica Spectrum Disorder
P2860
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P2860
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@en
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@nl
type
label
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@en
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@nl
prefLabel
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@en
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@nl
P2093
P2860
P356
P1476
Occurrence of acute large and edematous callosal lesions in neuromyelitis optica.
@en
P2093
I Miyazawa
K Fujihara
M Nakamura
S Watanabe
T Takahashi
P2860
P304
P356
10.1177/1352458509103301
P577
2009-05-12T00:00:00Z