Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Rudolf K F Oliveira"'
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 50, Iss 4 (2024)
Externí odkaz:
https://doaj.org/article/4803b0a12307476a9e0e1c89299d565f
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 50, Iss 2 (2024)
Externí odkaz:
https://doaj.org/article/9f8d7560d0484982b86b00b3c28a3e00
Autor:
Ana Paula S Oliveira, Amanda T Campoy, Rudolf K F Oliveira, Jaquelina S Ota-Arakaki, Eloara V M Ferreira
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 49, Iss 5 (2023)
Externí odkaz:
https://doaj.org/article/230a2efbd1484e369a9e7436b61e6d72
Autor:
Annelieke C M J van Riel, David M Systrom, Rudolf K F Oliveira, Michael J Landzberg, Barbara J M Mulder, Berto J Bouma, Bradley A Maron, Amil M Shah, Aaron B Waxman, Alexander R Opotowsky
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179053 (2017)
We recently reported a novel observation that many patients with equal resting supine right ventricular(RV) and pulmonary artery(PA) systolic pressures develop an RV outflow tract(RVOT) pressure gradient during upright exercise. The current work deta
Externí odkaz:
https://doaj.org/article/3d05ec1d6ec74203b007548de3fdec01
Autor:
Michael H. Lee, Thaís C. F. Menezes, Julie A. Reisz, Eloara V. M. Ferreira, Brian B. Graham, Rudolf K. F. Oliveira
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Pulmonary arterial hypertension is an incurable disease marked by dysregulated metabolism, both at the cellular level in the pulmonary vasculature, and at the whole-body level characterized by impaired exercise oxygen consumption. Though both altered
Externí odkaz:
https://doaj.org/article/795a395e5114404493146bab8c48b38b
Autor:
Rudolf K. F. Oliveira, Peter S. Nyasulu, Adeel Ahmed Iqbal, Muhammad Hamdan Gul, Eloara V. M. Ferreira, John William Leclair, Zin Mar Htun, Luke S. Howard, Ana O. Mocumbi, Andrew J. Bryant, Jacques L. Tamuzi, Sergey Avdeev, Nicola Petrosillo, Ahmed Hassan, Ghazwan Butrous, Vinicio de Jesus Perez
Publikováno v:
Frontiers in medicine. 9
COVID-19 infection primarily targets the lungs, which in severe cases progresses to cytokine storm, acute respiratory distress syndrome, multiorgan dysfunction, and shock. Survivors are now presenting evidence of cardiopulmonary sequelae such as pers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4762f281138021f9db3bbc45c4cc25ab
https://pubmed.ncbi.nlm.nih.gov/36530872
https://pubmed.ncbi.nlm.nih.gov/36530872
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 47, Iss 5 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80fb6cf282a303a9edaba590d57478f8
https://doi.org/10.36416/1806-3756/e20210406
https://doi.org/10.36416/1806-3756/e20210406
Autor:
Inderjit, Singh, Farbod N, Rahaghi, Robert, Naeije, Rudolf K F, Oliveira, David M, Systrom, Aaron B, Waxman
Publikováno v:
Chest. 156(5)
Right ventricular (RV) dysfunction is associated with shortened life expectancy in heart failure with preserved ejection fraction (HFpEF). The contribution of pulmonary vascular dysfunction to RV dysfunction in HFpEF is not well understood.We investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::742db8b1d365b74bce006e3de9710041
https://pubmed.ncbi.nlm.nih.gov/31103695
https://pubmed.ncbi.nlm.nih.gov/31103695
Autor:
Rudolf K F, Oliveira, Rudolf K F, de Oliveira, Eloara V M, Ferreira, Roberta P, Ramos, Carolina M S, Messina, Carlos E B, Kapins, Célia M C, Silva, Jaquelina S, Ota-Arakaki
Publikováno v:
The Journal of Heart and Lung Transplantation. 33:157-162
Background Pulmonary arterial hypertension (PAH) is characterized by a pulmonary capillary wedge pressure (PCWP) of ≤15 mm Hg, given a normal left ventricular filling pressure (LVFP). However, recent studies have shown that, in PAH patients, diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fbc098332a4f4e0b2a8f7acc896fd8
https://doi.org/10.1016/j.healun.2013.10.008
https://doi.org/10.1016/j.healun.2013.10.008
Autor:
Jean Pierre Sibomana, Aloma Campeche, Roberto J. Carvalho-Filho, Ricardo Amorim Correa, Helena Duani, Virginia Pacheco Guimaraes, Joan F. Hilton, Biruk Kassa, Rahul Kumar, Michael H. Lee, Camila M. C. Loureiro, Sula Mazimba, Claudia Mickael, Rudolf K. F. Oliveira, Jaquelina S. Ota-Arakaki, Camila Farnese Rezende, Luciana C. S. Silva, Edford Sinkala, Hanan Yusuf Ahmed, Brian B. Graham
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Pulmonary arterial hypertension (PAH) is a disease of the lung blood vessels that results in right heart failure. PAH is thought to occur in about 5% to 10% of patients with hepatosplenic schistosomiasis, particularly due to S. mansoni. The lung bloo
Externí odkaz:
https://doaj.org/article/305f8bf524b54848967de4207fdbe852