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Results of the combined U.S. multicenter postapproval study of the Nit‐Occlud PDA device for percutaneous closure of patent ductus arteriosus

OBJECTIVES: To report the results of the Nit‐Occlud PDA prospective postapproval study (PAS) along with a comparison to the results of the pivotal and continued access trials. BACKGROUND: The Nit‐Occlud PDA (PFM Medical, Cologne, Germany), a nitinol coil patent ductus arteriosus (PDA) occluder, was...

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Detalhes bibliográficos
Publicado no:Catheter Cardiovasc Interv
Main Authors: Kobayashi, Daisuke, Salem, Morris M., Forbes, Thomas J., Gordon, Brent M., Soriano, Brian D., Dimas, Vivian, Goldstein, Bryan H., Owada, Carl, Javois, Alexander, Bass, John, Jones, Thomas K., Berman, Darren P., Gillespie, Matthew J., Moore, John W., Levi, Daniel S.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6587820/
https://ncbi.nlm.nih.gov/pubmed/30511498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccd.27995
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