Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Nicola, Benjamin"'
Autor:
Nicola Benjamin, Ishan Echampati, Satenik Harutyunova, Christina Alessandra Eichstaedt, Benjamin Egenlauf, Silvia Ulrich, Ekkehard Grünig, Panagiota Xanthouli
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Current guidelines recommend oxygen (O2) supplementation in patients with pulmonary hypertension (PH), despite scarce data on long-term O2 therapy (LTOT). The aim of this prospective, randomized, controlled trial was to investigate the effec
Externí odkaz:
https://doaj.org/article/28f7e5426c1c444781cdbe1328ccd1ec
Autor:
Panagiota Xanthouli, Paul Uesbeck, Hanns-Martin Lorenz, Norbert Blank, Christina A. Eichstaedt, Satenik Harutyunova, Benjamin Egenlauf, Jerry G. Coghlan, Christopher P. Denton, Ekkehard Grünig, Nicola Benjamin
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-10 (2024)
Abstract Background In the EDITA trial, patients with systemic sclerosis (SSc) and mild pulmonary vascular disease (PVD) treated with ambrisentan had a significant decline of pulmonary vascular resistance (PVR) but not of mean pulmonary arterial pres
Externí odkaz:
https://doaj.org/article/2e2c26b4390045a1b2e87baf0744e937
Autor:
Eglė Palevičiūtė, Jelena Čelutkienė, Toma Šimbelytė, Lina Gumbienė, Elena Jurevičienė, Diana Zakarkaitė, Sigitas Čėsna, Christina A. Eichstaedt, Nicola Benjamin, Ekkehard Grünig
Publikováno v:
Trials, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background Left heart failure (HF) is characterized by an elevation in left-sided filling pressures, causing symptoms of dyspnea, impairing exercise capacity, and leading to pulmonary venous congestion and secondary pulmonary hypertension (P
Externí odkaz:
https://doaj.org/article/dad2e4a724c847f295d433cd9310b53b
Autor:
Panagiota Xanthouli, Ojan Gordjani, Nicola Benjamin, Satenik Harutyunova, Benjamin Egenlauf, Alberto M. Marra, Simon Haas, Nicklas Milde, Norbert Blank, Hanns-Martin Lorenz, Christoph Fiehn, Silvia Ulrich, Oliver Distler, Ekkehard Grünig, Christina A. Eichstaedt
Publikováno v:
Arthritis Research & Therapy, Vol 25, Iss 1, Pp 1-11 (2023)
Abstract Background Patients with systemic sclerosis (SSc) are frequently affected by iron deficiency, particularly those with pulmonary hypertension (PH). The first data indicate the prognostic importance of hypochromic red cells (% HRC) > 2% among
Externí odkaz:
https://doaj.org/article/bfabf2c64b1646229e90c883e4c2be99
Autor:
Panagiota Xanthouli, Ojan Gordjani, Nicola Benjamin, Franziska C. Trudzinski, Benjamin Egenlauf, Satenik Harutyunova, Alberto M. Marra, Nicklas Milde, Christian Nagel, Norbert Blank, Hanns-Martin Lorenz, Ekkehard Grünig, Christina A. Eichstaedt
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Oxygenated hemoglobin (OxyHem) in arterial blood may reflect disease severity in patients with systemic sclerosis (SSc). The aim of this study was to analyze the predictive value of OxyHem in SSc patients screened for pulmonary hypertension
Externí odkaz:
https://doaj.org/article/ca79233d5db74dda8cf780ae95332587
Autor:
Julia Degering, Benjamin Egenlauf, Satenik Harutyunova, Nicola Benjamin, Amina Salkić, Panagiota Xanthouli, Christina A. Eichstaedt, Rebekka Seeger, Olivier Sitbon, Ekkehard Grünig
Publikováno v:
Respiratory Research, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Background Epoprostenol AS (Veletri®), a thermostable epoprostenol formulation, provides better drug stability and improved clinical use compared to previous epoprostenol formulations. This study aims to expand clinical experience in the us
Externí odkaz:
https://doaj.org/article/856e097475d048c79383c6f372a7dd44
Autor:
Max Wissmüller, Panagiota Xanthouli, Nicola Benjamin, Ekkehard Grünig, Manuel J. Richter, Henning Gall, Hossein Ardeschir Ghofrani, Simon Herkenrath, Dirk Skowasch, Carmen Pizarro, Michael Halank, Christopher Hohmann, Martin Hellmich, Felix Gerhardt, Stephan Rosenkranz
Publikováno v:
ESC Heart Failure, Vol 9, Iss 5, Pp 2873-2885 (2022)
Abstract Aims Guideline recommendations highlight the critical role of combination therapy for the treatment of pulmonary arterial hypertension (PAH). Conversely, registry data demonstrate that a considerable number of PAH patients remain on monother
Externí odkaz:
https://doaj.org/article/67c894d4e963415ba31c6457b88091e3
Autor:
Panagiota Xanthouli, Julia Miazgowski, Nicola Benjamin, Ojan Gordjani, Benjamin Egenlauf, Satenik Harutyunova, Rebekka Seeger, Alberto M. Marra, Norbert Blank, Hanns-Martin Lorenz, Ekkehard Grünig, Christina A. Eichstaedt
Publikováno v:
Arthritis Research & Therapy, Vol 24, Iss 1, Pp 1-16 (2022)
Abstract Background The objective of this study was to investigate the prognostic impact of right ventricular (RV) function at rest and during exercise in patients with systemic sclerosis (SSc) presenting for a screening for pulmonary hypertension (P
Externí odkaz:
https://doaj.org/article/be39144d11724fb5ad34b263576f2534
Autor:
Vivienne Theobald, Ekkehard Grünig, Nicola Benjamin, Hans‐Jürgen Seyfarth, Michael Halank, Marc A. Schneider, Sarah Richtmann, Daniel Kazdal, Katrin Hinderhofer, Panagiota Xanthouli, Benjamin Egenlauf, Satenik Harutyunova, Marius M. Hoeper, Danny Jonigk, Richard Sparla, Martina U. Muckenthaler, Christina A. Eichstaedt
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 2, Pp n/a-n/a (2023)
Abstract Iron deficiency is common in idiopathic and heritable pulmonary arterial hypertension patients (I/HPAH). A previous report suggested a dysregulation of the iron hormone hepcidin, which is controlled by BMP/SMAD signaling involving the bone m
Externí odkaz:
https://doaj.org/article/06906adb9d074ed8bf1540d8e0c8f963
Autor:
Christina A. Eichstaedt, Zoe Saßmannshausen, Memoona Shaukat, Ding Cao, Panagiota Xanthouli, Henning Gall, Natascha Sommer, Hossein-Ardeschir Ghofrani, Hans-Jürgen Seyfarth, Marianne Lerche, Michael Halank, Janina Kleymann, Nicola Benjamin, Satenik Harutyunova, Benjamin Egenlauf, Katrin Milger, Stephan Rosenkranz, Ralf Ewert, Hans Klose, Marius M. Hoeper, Karen M. Olsson, Mareike Lankeit, Tobias J. Lange, Katrin Hinderhofer, Ekkehard Grünig
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-12 (2022)
Abstract Background A genetic predisposition can lead to the rare disease pulmonary arterial hypertension (PAH). Most mutations have been identified in the gene BMPR2 in heritable PAH. However, as of today 15 further PAH genes have been described. Th
Externí odkaz:
https://doaj.org/article/1de528004b62464999a9e805a210de5e