Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Klinger, James R"'
Autor:
DuBrock, Hilary M., Burger, Charles D., Bartolome, Sonja D., Feldman, Jeremy P., Ivy, D. Dunbar, Rosenzweig, Erika B., Sager, Jeffrey S., Presberg, Kenneth W., Mathai, Stephen C., Lammi, Matthew R., Klinger, James R., Eggert, Michael, De Marco, Teresa, Elwing, Jean M., Badesch, David, Bull, Todd M., Cadaret, Linda M., Ramani, Gautam, Thenappan, Thenappan, Ford, H. James, Al-Naamani, Nadine, Simon, Marc A., Mazimba, Sula, Runo, James R., Chakinala, Murali, Horn, Evelyn M., Ryan, John J., Frantz, Robert P., Krowka, Michael J.
Supplemental material, sj-pdf-1-pul-10.1177_20458940211020913 for Health disparities and treatment approaches in portopulmonary hypertension and idiopathic pulmonary arterial hypertension: an analysis of the Pulmonary Hypertension Association Registr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a87cc429550960e3513cc71363c090b4
Autor:
Ventetuolo, Corey, Aliotta, Jason, Braza, Julie, Chichger, Havovi, Dooner, Mark, McGuirl, Donald, Mullin, Chris, Newton, Julie, Pereira, Mandy, Princiotto, Amy, Quesenberry, Peter, Walsh, Thomas, Whittenhall, Mary, Klinger, James R., Harrington, Elizabeth O.
Endothelial dysfunction is a hallmark of pulmonary arterial hypertension (PAH) but there are no established methods to study pulmonary artery endothelial cells (PAECs) from living patients. We sought to culture PAECs from pulmonary artery catheter (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::2c046682e3f46214d669e00f58735bd5
https://arro.anglia.ac.uk/id/eprint/705034/4/Chichger_2019_2.docx
https://arro.anglia.ac.uk/id/eprint/705034/4/Chichger_2019_2.docx
Autor:
Taichman, Darren B, Ornelas, Joe, Chung, Lorinda, Klinger, James R, Lewis, Sandra, Mandel, Jess, Palevsky, Harold I, Rich, Stuart, Sood, Namita, Rosenzweig, Erika B, Trow, Terence K, Yung, Rex, Elliott, C Gregory, Badesch, David B
Publikováno v:
Chest, vol 146, iss 2
ObjectiveChoices of pharmacologic therapies for pulmonary arterial hypertension (PAH) are ideally guided by high-level evidence. The objective of this guideline is to provide clinicians advice regarding pharmacologic therapy for adult patients with P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::93815c1dfaf89eb659d1d65132516241
https://escholarship.org/uc/item/2gv951wx
https://escholarship.org/uc/item/2gv951wx
Publikováno v:
Pulmonary Medicine.
Pulmonary arterial hypertension is a rare disease, which requires a high index of suspicion to diagnose when patients initially present. Initial symptoms can be nonspecific and include complaints such as fatigue and mild dyspnea. Once the disease is
Autor:
Klinger, James R., Benza, Raymond L., Ghofrani, Hossein-Ardeschir, Jansa, Pavel, Gruenig, Ekkehard, Vizza, Dario, Meier, Christian, Busse, Dennis, Marius Hoeper
Publikováno v:
Publons
Web of Science
Web of Science
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::be9deaa54c48d6a969a271a65ff4bb9c
https://publons.com/publon/25943768/
https://publons.com/publon/25943768/