Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia von Harrison, R E, Flanagan, J A, Sankelo, M, Abdalla, S A, Rowell, J, Machado, R D, Elliott, C G, Robbins, I M, Olschewski, H, McLaughlin, V, Gruenig, E, Kermeen, F, Laitinen, T, Morrell, N W, Trembath, R C

Volltext

Macitentan tadalafil Fixed Dose Combination (FDC) in treatment-naive and prior monotherapy patients with Pulmonary Arterial Hypertension (PAH): insights from A DUE von Gruenig, E, Jansa, P, Fan, F, Friberg, M, Lassen, C, Pannaux, M, Rofael, H, Chin, K

Volltext

Efficacy and dose-response relationship of oral treprostinil in PAH patients on monotherapy or dual background therapy von Barbera, J A, Kiely, D, Gruenig, E, Balasubramanian, V, Vizza, C D, Elwing, J, Sood, N, Rao, Y, Holdstock, L, Seaman, S, Broderick, M, White, R J

Volltext

Changes in cMRI parameters following a switch to riociguat from phosphodiesterase type 5 inhibitors (PDE5i) in patients with pulmonary arterial hypertension: a REPLACE substudy von Rosenkranz, S, Benza, R L, Ghofrani, H A, Gruenig, E, Hoeper, M M, Peacock, A, Simonneau, G, Vizza, D, Meier, C, Vogtlaender, K, Vonk-Noordegraaf, A

Volltext

P1628Safety and efficacy of immunoadsorption as an add-on to medical treatment in patients with severe idiopathic pulmonary arterial hypertension (IPAH) von Egenlauf, B, Nagel, C, Ewert, R, Lehmkuhl, H, Rosenkranz, S, Benjamin, N, Schwenger, V, Herth, F, Gruenig, E

Volltext

C71 CRYSTAL BALL: CLINICAL FEATURES OF PULMONARY VASCULAR DISEASE II: Circulating Micro-Rna In Pulmonary Arterial Hypertension In Patients Who Receive Add-On Therapy With Exercise... von Grunig, G, Eichstaedt, C A, Saxer, S, Bloch, K E, Ulrich, S, Gruenig, E, Pylawka, S

Volltext

Pulmonary arterial hypertension-related myopathy: An overview of current data and future perspectives von Marra, A.M, Arcopinto, M, Bossone, E, Ehlken, N, Cittadini, A, Grünig, E

Volltext

Genetic counselling and testing in pulmonary arterial hypertension - A consensus statement on behalf of the International Consortium for Genetic Studies in PAH - French version von Montani, D, Eichstaedt, C.A, Belge, C, Chung, W.K, Graef, S, Gruenig, E, Humbert, M, Quarck, R, Tenorio-Castano, J.A, Soubrier, F, Trembath, R.C, Morrell, N.W

Volltext

P4534Reduced right ventricular contractile reserve in patients with systemic sclerosis and borderline pulmonary arterial pressures von Marra, A M, Nagel, C, Benjamin, N, Blank, N, Cittadini, A, Coghlan, G, Distler, O, Denton, C P, Fiehn, C, Egenlauf, B, Xanthouli, P, Hoeper, M M, Lorenz, H M, Bossone, E, Gruenig, E

Volltext

Clinical outcomes stratified by baseline functional class after initial combination therapy for pulmonary arterial hypertension von White, RJ, Vonk-Noordegraaf, A, Rosenkranz, S, Oudiz, RJ, McLaughlin, VV, Hoeper, MM, Gruenig, E, Ghofrani, H-A, Chakinala, MM, Barbera, JA, Blair, C, Langley, J, Frost, AE

Volltext

Solvent-Induced Crystallization of Poly(phenylene sulfone) von Grünig, Lara E, Meyer, Andreas, Emmler, Thomas, Abetz, Volker, Handge, Ulrich A

Volltext

The role of gas exchange measurements during exercise in the detection of early pulmonary arterial hypertension in scleroderma patients - a multi-center analysis von Dumitrescu, D., Kovacs, G., Nagel, C., Halank, M., Winkler, J., Gruenig, E., Olschewski, H., Ewert, R., Rosenkranz, S.

Volltext

Genetic Association of the Serotonin Transporter in Pulmonary Arterial Hypertension von Machado, Rajiv D, Koehler, Rolf, Glissmeyer, Eric, Veal, Colin, Suntharalingam, Jay, Kim, Miryoung, Carlquist, John, Town, Margaret, Elliott, C. Gregory, Hoeper, Marius, Fijalkowska, Anna, Kurzyna, Marcin, Thomson, Jennifer R, Gibbs, Simon R, Wilkins, Martin R, Seeger, Werner, Morrell, Nicholas W, Gruenig, Ekkehard, Trembath, Richard C, Janssen, Bart

Volltext

Pulmonary hypertension: Possible genetic causes and therapeutic options von Grünig, E, Eichstaedt, C A, Ehlken, N, Mayer, E, Klose, H

Volltext

Assessment of reproducibility and stability of different breath-hold maneuvres by dynamic MRI: comparison between healthy adults and patients with pulmonary hypertension von Plathow, Christian, Ley, Sebastian, Zaporozhan, Julia, Schöbinger, Max, Gruenig, Ekkehard, Puderbach, Michael, Eichinger, Monika, Meinzer, Hans-Peter, Zuna, Ivan, Kauczor, Hans-Ulrich

Volltext

First experiences with the stable prostacyclin analog iloprost in the evaluation of heart transplant candidates with increased pulmonary vascular resistance von Sablotzki, Armin, Czeslick, Elke, Gruenig, Ekkehard, Friedrich, Ivar, Schubert, Susann, Börgermann, Jochen, Hentschel, Thomas

Volltext

Multicenter standardization of phase-resolved functional lung MRI in patients with suspected chronic thromboembolic pulmonary hypertension von Moher Alsady, T, Voskrebenzev, A, Behrendt, L, Olsson, K, Heußel, C.P, Gruenig, E, Gall, H, Ghofrani, A, Roller, F, Harth, S, Marshall, H, Hughes, P.J.C, Wild, J, Swift, A.J, Kiely, D.G, Behr, J, Dinkel, J, Beitzke, D, Lang, I.M, Schmidt, K.H, Kreitner, K.F, Frauenfelder, T, Ulrich, S, Hamer, O.W, Vogel‐Claussen, J

Volltext bestellen

Exercise induced increase of pulmonary artery pressure (PAP) is associated with ventilation/perfusion missmatch in healthy family members of primary pulmonary hypertension (PPH) in... von Dehnert, C, Gruenig, E, Mereles, D, Arnold, K, Kuebler, W, Baertsch, P

Volltext

Niedrig dosierte Atem- und Bewegungstherapie verbessert die körperliche Leistungsfähigkeit und die Lebensqualität bei Patienten mit schwerer chronischer pulmonaler Hypertonie von Ehlken, N, Mereles, D, Ghofrani, A, Hoeper, M, Halank, M, Meyer, J, Karger, G, Wilkens, H, Herth, F, Olschewski, H, Gruenig, E

Volltext

1138 Assessment of right ventricular function during exercise by strain or strain rate imaging and ventilatory response in patients with severe pulmonary arterial hypertension von FILUSCH, A, SCHOENE, P, HANSEN, A, BUSS, S, GRUENIG, E, MEYER, F, KUECHERER, H

Volltext