Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Shahin, Moledina"'
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 6 (2023)
Background Transthoracic echocardiography is part of the regular follow‐up protocol at most pediatric pulmonary arterial hypertension (PAH) centers. We aimed to develop a comprehensive and simple echocardiographic risk stratification for children w
Externí odkaz:
https://doaj.org/article/e1a9f707a10f4444a277e50c74d6e48e
Publikováno v:
Breathe, Vol 18, Iss 4 (2022)
Pulmonary hypertension (PH) can develop in babies with bronchopulmonary dysplasia (BPD). PH is common in those with severe BPD and is associated with a high mortality rate. However, in babies surviving beyond 6 months, resolution of PH is likely. The
Externí odkaz:
https://doaj.org/article/fb17ee9d866246c4b1160b1c88b73b13
Autor:
Humberto García Aguilar, Matthias Gorenflo, D. Dunbar Ivy, Shahin Moledina, Biagio Castaldi, Hidekazu Ishida, Paweł Cześniewicz, Jacek Kusa, Oliver Miera, Joseph Pattathu, Ken‐Pen Weng, Laszlo Ablonczy, Christian Apitz, Marta Katona, Kenichi Kurosaki, Tomas Pulido, Hiroyuki Yamagishi, Kazushi Yasuda, Galia Cisternas, Melanie Goth, Susanne Lippert, Anna Radomskyj, Soundos Saleh, Stefan Willmann, Gabriela Wirsching, Damien Bonnet, Maurice Beghetti
Publikováno v:
Pulmonary Circulation, Vol 12, Iss 3, Pp n/a-n/a (2022)
Abstract Riociguat, a soluble guanylate cyclase stimulator, is approved for treatment of adults with pulmonary arterial hypertension (PAH). The safety, tolerability, and pharmacokinetics (PK) of oral riociguat in a pediatric population with PAH was a
Externí odkaz:
https://doaj.org/article/b9ede33b5c434f00ad5c57409c295608
Autor:
Hythem Nawaytou, Jeffrey R. Fineman, Shahin Moledina, Dunbar Ivy, Steven H. Abman, Maria J. Del Cerro
Publikováno v:
Pulmonary Circulation, Vol 11 (2021)
Development of pulmonary hypertension (PH) in patients with left side heart disease (LHD) is a predictor of poor prognosis. The use of pulmonary vasodilators in PH associated with LHD (PH-LHD) is controversial. In this study, we describe the practice
Externí odkaz:
https://doaj.org/article/578b4bb3b7024207bab63c6d9e2d90c6
Autor:
Stefan Gräf, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen M. Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Micheala Aldred, Harm J. Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Cesare Danesino, Mélanie Eyries, Henning Gall, Stefano Ghio, Hossein-Ardeschir Ghofrani, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Luke Howard, Marc Humbert, David G. Kiely, Gabor Kovacs, Robert V. MacKenzie Ross, Shahin Moledina, David Montani, Michael Newnham, Andrea Olschewski, Horst Olschewski, Andrew J. Peacock, Joanna Pepke-Zaba, Inga Prokopenko, Christopher J. Rhodes, Laura Scelsi, Werner Seeger, Florent Soubrier, Dan F. Stein, Jay Suntharalingam, Emilia M. Swietlik, Mark R. Toshner, David A. van Heel, Anton Vonk Noordegraaf, Quinten Waisfisz, John Wharton, Stephen J. Wort, Willem H. Ouwehand, Nicole Soranzo, Allan Lawrie, Paul D. Upton, Martin R. Wilkins, Richard C. Trembath, Nicholas W. Morrell
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-16 (2018)
Pulmonary arterial hypertension (PAH) is a rare lung disorder characterised by narrowing and obliteration of small pulmonary arteries ultimately leading to right heart failure. Here, the authors sequence whole genomes of over 1000 PAH patients and id
Externí odkaz:
https://doaj.org/article/cb3171b4e79940aa9ab812b5a9ce621a
Autor:
Lina Caicedo, Rachel Hopper, Humberto Garcia Aguilar, Dunbar Ivy, Dora Haag, Jeff Fineman, Tillman Humpl, Omar Al-Tamimi, Jeff A. Feinstein, Rolf Berger, Erika Rosenzweig, Tarek Kashour, Gabriel Fernando Diaz, Alberto Mendoza, Usha Krishnan, Prashant Bobhate, Stephanie Handler, Antonio Augusto Lopes, Manoj Kumar Rahit, Parag Barward, Carlos Labrandero de Lera, Ian Adatia, Shahin Moledina, Steven Abman, Maria Jesus del Cerro
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
The aim of this study was to determine practice patterns and inter-institutional variability in how acute vasoreactivity testing (AVT) is performed and interpreted in pediatrics throughout the world. A survey was offered to physicians affiliated with
Externí odkaz:
https://doaj.org/article/db2439c1407645bdab4dd5ea64be3cae
Autor:
David G. Kiely, David L. Levin, Paul M. Hassoun, Dunbar Ivy, Pei-Ni Jone, Jumaa Bwika, Steven M. Kawut, Jim Lordan, Angela Lungu, Jeremy A. Mazurek, Shahin Moledina, Horst Olschewski, Andrew J. Peacock, G.D. Puri, Farbod N. Rahaghi, Michal Schafer, Mark Schiebler, Nicholas Screaton, Merryn Tawhai, Edwin J.R. van Beek, Anton Vonk-Noordegraaf, Rebecca Vandepool, Stephen J. Wort, Lan Zhao, Jim M. Wild, Jens Vogel-Claussen, Andrew J. Swift
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
Pulmonary hypertension (PH) is highly heterogeneous and despite treatment advances it remains a life-shortening condition. There have been significant advances in imaging technologies, but despite evidence of their potential clinical utility, practic
Externí odkaz:
https://doaj.org/article/07df8bbb28ba42c3be4075e16f90f3ba
Autor:
Javier Gavela, Sudivya Sharma, Dominic Thompson, Alessandra Cocca, Timothy Thiruchelvam, Shahin Moledina
Publikováno v:
Journal of Paediatrics and Child Health. 58:1872-1875
Autor:
R. Mark Grady, Matthew W. Canter, Fei Wan, Anton A. Shmalts, Ryan D. Coleman, Maurice Beghetti, Rolf M.F. Berger, Maria J. del Cerro Marin, Scott E. Fletcher, Russel Hirsch, Tilman Humpl, D. Dunbar Ivy, Edward C. Kirkpatrick, Thomas J. Kulik, Marilyne Levy, Shahin Moledina, Delphine Yung, Pirooz Eghtesady, Damien Bonnet, S. Melissa Magness, Venus R. Anderson, Mary M. Mullen, Sergey V. Gorbachevsky, Sergey B. Zaets, Meindina G. Haarman, Isabelle Szezepanski
Publikováno v:
Journal of the American College of Cardiology, 78(5), 468-477. ELSEVIER SCIENCE INC
J Am Coll Cardiol
J Am Coll Cardiol
BACKGROUND: The placement of a pulmonary-to-systemic arterial shunt in children with severe pulmonary hypertension (PH) has been demonstrated, in relatively small studies, to be an effective palliation for their disease.OBJECTIVES: The aim of this st
Autor:
Andrew Constantine, Konstantinos Dimopoulos, Sheila G. Haworth, Vivek Muthurangu, Shahin Moledina
Publikováno v:
American journal of respiratory and critical care medicine. 206(6)
Rationale: Pediatric pulmonary hypertension is an important cause of childhood morbidity and mortality, but there are limited data on the range of associated diseases, contributions of different pulmonary hypertension subtypes, therapeutic strategies