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Expert Opinion on Investigational Drugs Volume 20, 2011 - Issue 5
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Key Paper Evaluation

Inhaled phosphodiesterase type 5 inhibitors for cystic fibrosis: a new therapy for systemic disease?

Evaluation of: Lubamba B, Lebacq J, Reychler G, et al. Inhaled phosphodiesterase type 5 inhibitors restore chloride transport in cystic fibrosis mice. Eur Respir J 37(1):72-78.

Sabina Antonela Antoniu University of Medicine and Pharmacy “Gr.T.Popa” Iasi, Department of Internal Medicine II-Pulmonary Disease, Pulmonary Disease University Hospital, 30 Dr I Cihac Str, 700115 Iasi, Romania +40 232 239408; +40 232 270918; [email protected]
, MD PhD
Pages 713-715 | Published online: 24 Mar 2011

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