Protocol for the EARCO Registry: a pan-European observational study in patients with α(1)-antitrypsin deficiency

RATIONALE AND OBJECTIVES: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to an increased risk of emphysema and liver disease. Despite extensive investigation, there remain unanswered questions concerning the natural history, pathophysiology, genetics and the prognosis of the...

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Detaylı Bibliyografya
Yayımlandı:ERJ Open Res
Asıl Yazarlar: Greulich, Timm, Altraja, Alan, Barrecheguren, Miriam, Bals, Robert, Chlumsky, Jan, Chorostowska-Wynimko, Joanna, Clarenbach, Christian, Corda, Luciano, Corsico, Angelo Guido, Ferrarotti, Ilaria, Esquinas, Cristina, Gouder, Caroline, Hećimović, Ana, Ilic, Aleksandra, Ivanov, Yavor, Janciauskiene, Sabina, Janssens, Wim, Kohler, Malcolm, Krams, Alvils, Lara, Beatriz, Mahadeva, Ravi, McElvaney, Gerry, Mornex, Jean-François, O'Hara, Karen, Parr, David, Piitulainen, Eava, Schmid-Scherzer, Karin, Seersholm, Niels, Stockley, Robert A., Stolk, Jan, Sucena, Maria, Tanash, Hanan, Turner, Alice, Ulmeanu, Ruxandra, Wilkens, Marion, Yorgancioğlu, Arzu, Zaharie, Ana, Miravitlles, Marc
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: European Respiratory Society 2020
Konular:
Study Protocol
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7049712/
https://ncbi.nlm.nih.gov/pubmed/32154291
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1183/23120541.00181-2019
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