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High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

BACKGROUND: Patients with congenital heart disease (CHD) and heterotaxy show high postsurgical morbidity/mortality, with some developing respiratory complications. Although this finding is often attributed to the CHD, airway clearance and left-right patterning both require motile cilia function. Thu...

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Detalhes bibliográficos
Main Authors: Nakhleh, Nader, Francis, Richard, Giese, Rachel A., Tian, Xin, Li, You, Zariwala, Maimoona A., Yagi, Hisato, Khalifa, Omar, Kureshi, Safina, Chatterjee, Bishwanath, Sabol, Steven L., Swisher, Matthew, Connelly, Patricia S., Daniels, Mathew P., Srinivasan, Ashok, Kuehl, Karen, Kravitz, Nadav, Burns, Kimberlie, Sami, Iman, Omran, Heymut, Barmada, Michael, Olivier, Kenneth, Chawla, Kunal K., Leigh, Margaret, Jonas, Richard, Knowles, Michael, Leatherbury, Linda, Lo, Cecilia W.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3770728/
https://ncbi.nlm.nih.gov/pubmed/22499950
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCULATIONAHA.111.079780
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