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Neuromyelitis Optica [PDF]

open access: yesIndian Journal of Physical Medicine & Rehabilitation, 2009
Neuromyelitis optica (NMO) is a rare, idiopathic,inflammatory disease affecting the spine andcharacteristically sparing the brain. It mimics multiplesclerosis (MS) in many aspects.
Goyal V, Rooru S, Gafoor AS, Sreekala VK
doaj   +4 more sources

Neuromyelitis optica

open access: yesAnnals of Indian Academy of Neurology, 2007
Neuromyelitis optica (NMO) or Devic′s disease was until recently regarded as an unusual or severe variant of multiple sclerosis. However the last decade has seen major advances in our understanding of the etiopathogenesis of NMO. Though unsettled,
Jacob Anu, Boggild Mike
doaj   +5 more sources

Co-occurrence of aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder and hepatocellular carcinoma: A case report [PDF]

open access: yesJournal of International Medical Research
Neuromyelitis optica spectrum disorder is a rare, relapsing autoimmune disease in which the immune system attacks the central nervous system, primarily the optic nerves and spinal cord.
Cheng Li, Weijing Liao, Di Long
doaj   +2 more sources

The patient journey with NMOSD: From initial diagnosis to chronic condition

open access: yesFrontiers in Neurology, 2022
ObjectiveTo better understand the patient experience with neuromyelitis optica spectrum disorder (NMOSD) through the course of the illness.BackgroundNMOSD is a rare autoimmune disorder that causes recurrent inflammatory attacks of the optic nerve, spinal
Guillermo Delgado-Garcia   +4 more
doaj   +1 more source

Neuromyelitis optica spectrum disorders [PDF]

open access: yesTherapeutic Advances in Neurological Disorders
Mohammad Ali Sahraian, Kazuo Fujihara
doaj   +2 more sources

Neuromyelitis Optica [PDF]

open access: yesRheumatic Disease Clinics of North America, 2017
Neuromyelitis optica (NMO), formerly known as Devic disease, is an autoimmune astrocytopathic disease characterized by transverse myelitis and optic neuritis. Most patients demonstrate a relapsing course with incomplete recovery between attacks, resulting in progressive disability.
Sarah L, Patterson, Sarah E, Goglin
openaire   +6 more sources

Neuromyelitis optica is an HLA associated disease different from Multiple Sclerosis: a systematic review with meta-analysis

open access: yesScientific Reports, 2021
Neuromyelitis Optica and Multiple Sclerosis are idiopathic inflammatory demyelinating diseases of the central nervous system that currently are considered distinct autoimmune diseases, so differences in genetic susceptibility would be expected.
Marcos Papais Alvarenga   +9 more
doaj   +1 more source

Neuromyelitis optica [PDF]

open access: yesTidsskrift for Den norske legeforening, 2013
Neuromyelitis optica (NMO) is a rare autoimmune inflammatory disease of the central nervous system that is characterized mainly by recurrent optic neuritis and longitudinally extensive transverse myelitis. The aim of this article is to present current knowledge on the clinical features, diagnosis, pathogenesis and treatment of the condition.The article
Silje Agnethe Stokke, Kvistad   +4 more
openaire   +2 more sources

Neuromyelitis optica

open access: yesAktuelle Neurologie, 2012
The discovery of serum autoantibodies against the astrocytic water channel aquaporin-4 (AQP4) as a biomarker of neuromyelitis optica (NMO, Devic syndrome) has revolutionized our understanding of this rare immune-mediated clinical entity and has provided a rationale for the use of therapeutic strategies targeting the humoral effector arm of autoimmune ...
B, Wildemann, S, Jarius, F, Paul
  +8 more sources

Epidemiology of myelin oligodendrocyte glycoprotein antibody-associated disease: a review of prevalence and incidence worldwide

open access: yesFrontiers in Neurology, 2023
Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is an inflammatory demyelinating disease of the central nervous system (CNS) with the presence of conformation-sensitive antibodies against MOG.
Jyh Yung Hor   +2 more
doaj   +1 more source

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