Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Nesrin Mogulkoc"'
Autor:
Ondřej Májek, Jakub Gregor, Nesrin Mogulkoć, Katarzyna Lewandowska, Martina Šterclová, Veronika Müller, Marta Hájková, Mordechai R Kramer, Jasna Tekavec-Trkanjec, Dragana Jovanović, Michael Studnicka, Natalia Stoeva, Klaus-Uwe Kirchgässler, Simona Littnerová, Ladislav Dušek, Martina Koziar Vašáková
Publikováno v:
PLoS ONE, Vol 17, Iss 9, p e0273854 (2022)
BackgroundThere is no clear evidence whether pirfenidone has a benefit in patients with probable or possible UIP, i.e. when idiopathic pulmonary fibrosis (IPF) is diagnosed with a lower degree of diagnostic certainty. We report on outcomes of treatme
Externí odkaz:
https://doaj.org/article/62d03fd7fced4bb68c72565e31432e8a
Autor:
Dragana M. Jovanovic, Martina Šterclová, Nesrin Mogulkoc, Katarzyna Lewandowska, Veronika Müller, Marta Hájková, Michael Studnicka, Jasna Tekavec-Trkanjec, Simona Littnerová, Martina Vašáková, the EMPIRE registry investigators
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Patients with idiopathic pulmonary fibrosis (IPF) frequently have multiple comorbidities, which may influence survival but go under-recognised in clinical practice. We therefore report comorbidity, antifibrotic treatment use and s
Externí odkaz:
https://doaj.org/article/3e8acd4648c840be8bf8eb43046c6c69
Autor:
Eyjolfur Gudmundsson, An Zhao, Nesrin Mogulkoc, Frouke van Beek, Tinne Goos, Christopher J. Brereton, Marcel Veltkamp, Robert Chapman, Hendrik W. van Es, Helen Garthwaite, Bahareh Gholipour, Melissa Heightman, Arjun Nair, Katarina Pontoppidan, Recep Savas, Asia Ahmed, Marie Vermant, Omer Unat, Alex Procter, Laurens De Sadeleer, Emma Denneny, Timothy Wallis, Mark Duncan, Magali Taylor, Stijn Verleden, Sam M. Janes, Daniel C. Alexander, Athol U. Wells, Joanna Porter, Mark G. Jones, Iain Stewart, Coline H.M. van Moorsel, Wim Wuyts, Joseph Jacob
Publikováno v:
ERJ Open Research, Vol 9, Iss 2 (2023)
Background Computer quantification of baseline computed tomography (CT) radiological pleuroparenchymal fibroelastosis (PPFE) associates with mortality in idiopathic pulmonary fibrosis (IPF). We examined mortality associations of longitudinal change i
Externí odkaz:
https://doaj.org/article/5fc5df0263ac47c19e2f6c8941a02396
Autor:
Abigél Margit Kolonics-Farkas, Martina Šterclová, Nesrin Mogulkoc, Katarzyna Lewandowska, Veronika Müller, Marta Hájková, Mordechai Kramer, Dragana Jovanovic, Jasna Tekavec-Trkanjec, Michael Studnicka, Natalia Stoeva, Simona Littnerová, Martina Vašáková
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Idiopathic pulmonary fibrosis (IPF) is a rare lung disease with poor prognosis. The diagnosis and treatment possibilities are dependent on the health systems of countries. Hence, comparison among countries is difficult due to data heterogeneity. Our
Externí odkaz:
https://doaj.org/article/b399851ef6f24b1fa825cc97e6b8ce39
Autor:
Tanja Tran, Martina Šterclová, Nesrin Mogulkoc, Katarzyna Lewandowska, Veronika Müller, Marta Hájková, Mordechai R. Kramer, Dragana Jovanović, Jasna Tekavec-Trkanjec, Michael Studnicka, Natalia Stoeva, Karel Hejduk, Ladislav Dušek, Samy Suissa, Martina Vašáková, for the EMPIRE registry
Publikováno v:
Respiratory Research, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Several registries of idiopathic pulmonary fibrosis (IPF) have been established to better understand its natural history, though their size and duration of follow-up are limited. Here, we describe the large European MultiPartner I
Externí odkaz:
https://doaj.org/article/9d4a56a4f4404f718e7719bee03526fd
Autor:
Eyjolfur Gudmundsson, An Zhao, Nesrin Mogulkoc, Iain Stewart, Mark G. Jones, Coline H.M. Van Moorsel, Recep Savas, Christopher J. Brereton, Hendrik W. Van Es, Omer Unat, Katarina Pontoppidan, Frouke Van Beek, Marcel Veltkamp, Bahareh Gholipour, Arjun Nair, Athol U. Wells, Sam M. Janes, Daniel C. Alexander, Joseph Jacob
Publikováno v:
EClinicalMedicine, Vol 38, Iss , Pp 101009- (2021)
Background: Idiopathic pulmonary fibrosis (IPF) and pleuroparenchymal fibroelastosis (PPFE) are known to have poor outcomes but detailed examinations of prognostic significance of an association between these morphologic processes are lacking. Method
Externí odkaz:
https://doaj.org/article/0adf401fc86f4683bd4a4ef3183d2393
Autor:
An Zhao, Eyjolfur Gudmundsson, Nesrin Mogulkoc, Mark G. Jones, Coline van Moorsel, Tamera J. Corte, Chiara Romei, Recep Savas, Christopher J. Brereton, Hendrik W. van Es, Helen Jo, Annalisa De Liperi, Omer Unat, Katarina Pontoppidan, Frouke van Beek, Marcel Veltkamp, Peter Hopkins, Yuben Moodley, Alessandro Taliani, Laura Tavanti, Bahareh Gholipour, Arjun Nair, Sam Janes, Iain Stewart, David Barber, Daniel C. Alexander, Athol U. Wells, Joseph Jacob
Publikováno v:
ERJ Open Research, Vol 7, Iss 3 (2021)
Externí odkaz:
https://doaj.org/article/5fc8a067bf734c7092265fdf13bf4748
Autor:
Argyris Tzouvelekis, Katerina Antoniou, Michael Kreuter, Matthew Evison, Torsten G. Blum, Venerino Poletti, Bogdan Grigoriu, Carlo Vancheri, Paolo Spagnolo, Theodoros Karampitsakos, Francesco Bonella, Athol Wells, Ganesh Raghu, Maria Molina-Molina, Daniel A. Culver, Elisabeth Bendstrup, Nesrin Mogulkoc, Stefano Elia, Jacques Cadranel, Demosthenes Bouros
Publikováno v:
ERJ Open Research, Vol 7, Iss 1 (2021)
Background Currently there is major lack of agreement on the diagnostic and therapeutic management of patients with idiopathic pulmonary fibrosis (IPF) and lung cancer. Our aim was to identify variations in diagnostic and management strategies across
Externí odkaz:
https://doaj.org/article/d91b60e33b774a85a9840f953bfad60f
Autor:
Demet Terek, Meral Kayikcioglu, Hakan Kultursay, Mete Ergenoglu, Mehmet Yalaz, Oktay Musayev, Nesrin Mogulkoc, Ilkben Gunusen, Mete Akisu, Nilgun Kultursay
Publikováno v:
Journal of Research in Medical Sciences, Vol 18, Iss 1, Pp 73-76 (2013)
This is the case report of a pregnant woman who refused pregnancy termination when diagnosed with pulmonary arterial hypertension (PAH) functional class 2-3 at the 24th week of gestation and of her newborn. A pregnant woman with PAH functional class
Externí odkaz:
https://doaj.org/article/b7f5b1c0968547a09985cf7ac465b7e3
Autor:
An Zhao, Eyjolfur Gudmundsson, Nesrin Mogulkoc, Coline van Moorsel, Tamera J. Corte, Chiara Romei, Robert Chapman, Tim J.M. Wallis, Emma Denneny, Tinne Goos, Recep Savas, Asia Ahmed, Christopher J. Brereton, Hendrik W. van Es, Helen Jo, Annalisa De Liperi, Mark Duncan, Katarina Pontoppidan, Laurens J. De Sadeleer, Frouke van Beek, Joseph Barnett, Gary Cross, Alex Procter, Marcel Veltkamp, Peter Hopkins, Yuben Moodley, Alessandro Taliani, Magali Taylor, Stijn Verleden, Laura Tavanti, Marie Vermant, Arjun Nair, Iain Stewart, Sam M. Janes, Alexandra L. Young, David Barber, Daniel C. Alexander, Joanna C. Porter, Athol U. Wells, Mark G. Jones, Wim A. Wuyts, Joseph Jacob
BackgroundIdiopathic pulmonary fibrosis (IPF) with co-existent emphysema, termed combined pulmonary fibrosis and emphysema (CPFE) may be associated with reduced FVC decline compared to non-CPFE IPF patients. We examined associations between mortality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e847c368680bf7fc13e095db02bd2fa0
https://doi.org/10.1101/2023.05.05.23289330
https://doi.org/10.1101/2023.05.05.23289330