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Ter Arkh ; 73(5): 43-5, 2001.
Artigo em Russo | MEDLINE | ID: mdl-11517747

RESUMO

AIM: To evaluate efficacy of synthetic leukocytic interferon (SLI) in patients with severe Adamantiadi-Behçet syndrome (ABS). MATERIALS AND METHODS: The trial enrolled 18 patients (11 men and 7 women aged 25 to 43 years) with severe ABS. The duration of the disease ranged from 1 to 12 years. Subcutaneous ABS injections in a dose 5 x 10(6) U/m2 for 8 weeks followed by 3 x 10(6) for 16 weeks. The results were estimated by standard clinical and biochemical indices. RESULTS: All 18 patients responded to the treatment. After the course of treatment 13 patients were in remission for 4-52 months. The rest of the patients were given one more course of treatment.


Assuntos
Antivirais/uso terapêutico , Síndrome de Behçet/tratamento farmacológico , Interferon Tipo I/uso terapêutico , Adulto , Antivirais/administração & dosagem , Síndrome de Behçet/diagnóstico , Feminino , Seguimentos , Humanos , Interferon Tipo I/administração & dosagem , Masculino , Proteínas Recombinantes , Fatores de Tempo
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