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Anti-cytokine therapy in fibrosing alveolitis: where are we now?

Idiopathic pulmonary fibrosis (IPF) is a condition that has a poor prognosis, with a median survival of 4-5 years irrespective of treatment. Ziesche et al (N Engl J Med 1999, 341: 1264-1269) describe an open randomised trial of 18 patients with IPF, unresponsive to corticosteroid treatment at high d...

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Dades bibliogràfiques
Autor principal: Millar, Ann
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2000
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC59532/
https://ncbi.nlm.nih.gov/pubmed/11667955
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/rr2
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