Posted in Rheumatology | Tagged clasificacion, Classification, Criteria, criterios, dermatomiositis, Dermatomyositis, polimiositis, Polymyositis, rheumatology. La dermatomiositis es un tipo de miopatía inflamatoria idiopática que afecta al la clasificación y la predicción del pronóstico en las miopatías inflamatorias. Introducción. la dermatomiositis (DM) se engloba dentro de las miopatías inflamatorias idiopáticas. La piel y el músculo esquelético son los órganos.

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Here we report our experience through the description and analysis of a series of patients. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. This item has received. This is of great importance as no myositis-specific antibodies had previously been detected in these clinical subgroups. dermatojiositis

Dermatomiositis juvenil

Subscribe to our Newsletter. Monitoring disease activity in juvenile dermatomyositis: In the year has been indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern. Print Send to a friend Export reference Mendeley Statistics.


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Clinical and histopathological characteristics were assessed alongside the results of laboratory tests and the treatments used. If you are a member of the AEDV: SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. La globulina inmune intravenosa es cara drematomiositis se necesitan repetidas dosis. Previous article Next article.

SJR uses a similar algorithm as the Google page rank; dermatomiosiits provides a quantitative and qualitative measure of the journal’s impact.

Previous article Next article. April Pages Hospital Universitario Germans Trias i Pujol.

Eighty percent of patients required 2 or more drugs to achieve disease control. Este tratamiento se usa para las enfermedades de la piel activas o cuando se han probado otros medicamentos pero han fallado.

Classification Criteria for Polymyositis and Dermatomyositis

In most patients, the disease has a good prognosis, although extended periods of treatment may be required. Continuing navigation will be considered as acceptance of this use. None of the patients had myositis-specific antibodies. Subscriber If you already have your login data, please click here.


Generalmente con antecedentes familiares positivos. July – August Pages Correlations between change in disease activity and changes in peripheral blood lymphocyte subsets in patients with juvenile dermatomyositis.

All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. Assessment and Follow-up of 20 Patients.

Bohan Am, Peter JB. J Rheumatol ; Read this article in English.

Miopatías inflamatorias ideopáticas by Hector Urquiza Santoyo on Prezi

Nineteen of the 20 patients included in the study were women. SRJ is a prestige metric based on the idea that not all citations are the same. The identification of target antigens that are recognized by these antibodies is essential for dermatomiositi better understanding of the pathogenesis of these diseases.