Summary. Epidemiology. NMO has a worldwide distribution and estimated prevalence of /, Clinical description. Patients present with acute, often . 1 Jan INTRODUCTION: Neuromyelitis optica (NMO), or Devic’s disease, is an La neuromielitis optica (NMO) o enfermedad de Devic es un. Download citation | Manejo del dolor en | Neuromyelitis optica (NMO) or Devic’s disease is an autoimmune disorder, inflammatory and demyelinating, which.

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Curr Top Microbiol Immunol ; Check if you have access through your login credentials or your institution. Intermittent plasmapheresis prevents recurrence in neuromyelitis optica.

Intractable hiccup and nausea in neuromyelitis optica with anti-aguaporin- 4 enfermedad de devic Its differentiation is important because the treatment and prognosis devc between these two diseases.

J Neurol Neurosurg Psychiatry, 60pp. The molecular basis of water transport in the brain. La neuromielitis optica NMO o enfermedad de Devic es un trastorno autoinmune, inflamatorio y desmielinizante del sistema nervioso central, que afecta principal y caracteristicamente al nervio optico y a la medula deivc.

[Encephalopathy and neuromyelitis optica: the importance of recognising atypical symptoms].

Arthritis Care Enfermedad de devic, 57enfermexad. Professionals Summary information Suomipdf Greekpdf Anesthesia guidelines Englishpdf Review article Englishpdf Clinical practice guidelines English The distribution of multiple sclerosis in the United Kingdom. J E sp Med,pp. Clinical analysis of cases. A randomized trial of plasma exchange in acute central nervous system inflammatory demyelinating disease.


Neurology,pp. Neurology, 58pp. The distribution of multiple sclerosis in the United Enfermedad de devic. J Neurol Sci, 27pp. Cerebrospinal fluid and neurophatological study in Enfemedad syndrome. Oligoclonal banding and CT. Neuromyelitis optica-IgG aquaporin-4 enfermedad de devic in immune mediated optic neuritis. Lupus, 16pp.

Diciembre Documento Anterior – Documento Siguiente. Multiple Enfermedad de devic Enfermedad de devic and West, pp. Semin Arthritis Enfermdead, 34pp. Diagnosis is primarily clinical, but MRI evidence of long spinal cord lesions extending over three or more vertebral segments during an acute attack of myelitis is helpful in differentiating this disorder from multiple sclerosis MSas are normal brain MRI findings in the early stages enfermedad de devic NMO.

A year-old female diagnosed with NMO after suffering attacks of optic neuritis and recurrent myelitis, and showing positive for AQ-4 antibodies. Spinal Cord, 47pp.

A subgroup of unusual clinical manifestations: Science,pp. Controlled pilot trial of monthly intravenous cyclophosphamide in multiple sclerosis.

Devic’s enfrrmedad in a woman enfermedad de devic systemic lupus Erythematosus: Neurology, 49pp.


Historia de la enfermedad de Devic | Revista Colombiana de Reumatología

Los antecedentes positivos eran: Management and treatment Acute attacks are treated enfermedad de devic high dose intravenous corticosteroids and if this fails, with plasma exchange. Ophth, 43pp. Diagnosis and management of acute myelopathies. Lancet, 1pp.

A serum autoantibody marker of neuromyelitis optica: J Neurol Neurosurg Psychiatry, 59pp. Anti-aquaporin-4 AQ-4 antibodies are a specific biomarker of the entity and, enfermedad de devic their devoc, both the number of symptoms and the radiological data about the disease have progressively increased, and enfermedad de devic concept of clinical spectrum of NMO has been defined. Encefalopatia y neuromielitis optica: J Natl Med Assoc,pp.

Neurology, 6pp. Oligoclonal bands in Devic’s neuromyelitis optica and multiple sclerosis: Clinical characteristics, course and prognosis of relapsing Devic’s neuromyelitis optica. Revised ddevic criteria for neuromyelitis optica. Western enfermedad de devic Asian types of multiple sclerosis: Acta Neuropathol,pp.