TY - JOUR
T1 - The Ariane-IPF ERS Clinical Research Collaboration: seeking collaboration through launch of a federation of European registries on idiopathic pulmonary fibrosis
AU - Cottin, V.
AU - Annesi-Maesano, I.
AU - Gunther, A.
AU - Galvin, L.
AU - Kreuter, M.
AU - Powell, P.
AU - Prasse, A.
AU - Reynolds, G.
AU - Richeldi, Luca
AU - Spagnolo, P.
AU - Valenzuela, C.
AU - Wijsenbeek, M.
AU - Wuyts, W. A.
AU - Crestani, B.
PY - 2019
Y1 - 2019
N2 - Rationale for a multinational registry\r\nIdiopathic pulmonary fibrosis (IPF) is the most prevalent of rare pulmonary diseases [1], and the most\r\nsevere of the chronic forms of idiopathic interstitial pneumonias, with rising incidence and prevalence [2–4].\r\nThe prognosis for people diagnosed with IPF is a median survival of 3–3.5 years [1].
AB - Rationale for a multinational registry\r\nIdiopathic pulmonary fibrosis (IPF) is the most prevalent of rare pulmonary diseases [1], and the most\r\nsevere of the chronic forms of idiopathic interstitial pneumonias, with rising incidence and prevalence [2–4].\r\nThe prognosis for people diagnosed with IPF is a median survival of 3–3.5 years [1].
KW - idiopathic pulmonary fibrosis
KW - idiopathic pulmonary fibrosis
UR - https://publicatt.unicatt.it/handle/10807/147405
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85066842194&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85066842194&origin=inward
U2 - 10.1183/13993003.00539-2019
DO - 10.1183/13993003.00539-2019
M3 - Article
SN - 1399-3003
VL - 53
SP - 1
EP - 6
JO - European Respiratory Journal
JF - European Respiratory Journal
IS - 5
ER -