Idiopathic pulmonary arterial hypertension phenotypes determined by cluster analysis from the COMPERA registry

The term idiopathic pulmonary arterial hypertension (IPAH) is used to categorize patients with pre-capillary pulmonary hypertension of unknown origin. There is considerable variability in the clinical presentation of these patients. Using data from the Comparative, Prospective Registry of Newly Init...

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Vydáno v:	The Journal of heart and lung transplantation Ročník 39; číslo 12; s. 1435
Hlavní autoři:	Hoeper, Marius M, Pausch, Christine, Grünig, Ekkehard, Klose, Hans, Staehler, Gerd, Huscher, Doerte, Pittrow, David, Olsson, Karen M, Vizza, Carmine Dario, Gall, Henning, Benjamin, Nicola, Distler, Oliver, Opitz, Christian, Gibbs, J Simon R, Delcroix, Marion, Ghofrani, H Ardeschir, Rosenkranz, Stephan, Ewert, Ralf, Kaemmerer, Harald, Lange, Tobias J, Kabitz, Hans-Joachim, Skowasch, Dirk, Skride, Andris, Jureviciene, Elena, Paleviciute, Egle, Miliauskas, Skaidrius, Claussen, Martin, Behr, Juergen, Milger, Katrin, Halank, Michael, Wilkens, Heinrike, Wirtz, Hubert, Pfeuffer-Jovic, Elena, Harbaum, Lars, Scholtz, Werner, Dumitrescu, Daniel, Bruch, Leonhard, Coghlan, Gerry, Neurohr, Claus, Tsangaris, Iraklis, Gorenflo, Matthias, Scelsi, Laura, Vonk-Noordegraaf, Anton, Ulrich, Silvia, Held, Matthias
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	United States 01.12.2020
Témata:	mortality cluster phenotypes pulmonary arterial hypertension survival
ISSN:	1557-3117, 1557-3117
On-line přístup:	Zjistit podrobnosti o přístupu
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