Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Ana, Reula"'
Autor:
Yin Ting Lam, Jean-François Papon, Mihaela Alexandru, Andreas Anagiotos, Miguel Armengot, Mieke Boon, Andrea Burgess, Nathalie Caversaccio, Suzanne Crowley, Sinan Ahmed D. Dheyauldeen, Nagehan Emiralioglu, Ela Erdem, Christine van Gogh, Yasemin Gokdemir, Onder Gunaydın, Eric G. Haarman, Amanda Harris, Isolde Hayn, Hasnaa Ismail-Koch, Bulent Karadag, Céline Kempeneers, Sookyung Kim, Natalie Lorent, Ugur Ozcelik, Charlotte Pioch, Anne-Lise ML Poirrier, Ana Reula, Jobst Roehmel, Panayiotis Yiallouros, Myrofora Goutaki
Publikováno v:
Clinical and Experimental Otorhinolaryngology, Vol 16, Iss 4, Pp 407-412 (2023)
Externí odkaz:
https://doaj.org/article/b2b677241c6f446290767afbff9355b3
Autor:
Ana Reula, Silvia Castillo-Corullón, Miguel Armengot, Guadalupe Herrera, Amparo Escribano, Francisco Dasí
Publikováno v:
Antioxidants, Vol 13, Iss 2, p 190 (2024)
Background: Primary Ciliary Dyskinesia (PCD) represents a rare condition marked by an abnormal mobility pattern of cilia and flagella, resulting in impaired mucociliary clearance. This deficiency leads to recurrent infections and persistent inflammat
Externí odkaz:
https://doaj.org/article/82454b6930a74902924213f8e528e496
Autor:
Yin Ting Lam, Jean-François Papon, Mihaela Alexandru, Andreas Anagiotos, Miguel Armengot, Mieke Boon, Andrea Burgess, Suzanne Crowley, Sinan Ahmed D. Dheyauldeen, Nagehan Emiralioglu, Ela Erdem Eralp, Christine van Gogh, Yasemin Gokdemir, Onder Gunaydın, Eric G. Haarman, Amanda Harris, Isolde Hayn, Hasnaa Ismail-Koch, Bülent Karadag, Céline Kempeneers, Sookyung Kim, Philipp Latzin, Natalie Lorent, Ugur Ozcelik, Charlotte Pioch, Anne-Lise M.L. Poirrier, Ana Reula, Jobst Roehmel, Panayiotis Yiallouros, on behalf of the EPIC-PCD team, Myrofora Goutaki
Publikováno v:
ERJ Open Research, Vol 9, Iss 3 (2023)
Background Sinonasal symptoms are a common feature of primary ciliary dyskinesia (PCD); however, literature about their severity and frequency, particularly during the life course, is scarce. Using baseline data from the Ear, nose and throat (ENT) Pr
Externí odkaz:
https://doaj.org/article/af2659ccbe26408ba0bf123c0d1ed6c3
Autor:
Laura E. Gardner, Katie L. Horton, Amelia Shoemark, Jane S. Lucas, Kim G. Nielsen, Helene Kobbernagel, Bruna Rubbo, Robert A. Hirst, Panayiotis Kouis, Nicola Ullmann, Ana Reula, Nisreen Rumman, Hannah M. Mitchison, Andreia Pinto, Charlotte Richardson, Anne Schmidt, James Thompson, René Gaupmann, Maciej Dabrowski, Pleasantine Mill, Siobhan B. Carr, Dominic P. Norris, Claudia E. Kuehni, Myrofora Goutaki, Claire Hogg
Publikováno v:
BMC Proceedings, Vol 14, Iss S8, Pp 1-17 (2020)
Abstract Primary ciliary dyskinesia (PCD) is an inherited ciliopathy leading to chronic suppurative lung disease, chronic rhinosinusitis, middle ear disease, sub-fertility and situs abnormalities. As PCD is rare, it is important that scientists and c
Externí odkaz:
https://doaj.org/article/5ddaaec13100438fb611c709038b90fa
Autor:
Andreas Anagiotos, Myrofora Goutaki, André Coste, Nagehan Emiralioglu, Amanda Harris, Andrea Burgess, Mieke Boon, Philipp Latzin, Jean François Papon, Eric G Haarman, Natalie Lorent, Yin Ting Lam, Mihaela Alexandru, Miguel Armengot, Emilie Bequignon, Ela Erdem, Sara-Lynn Hool, Bulent Karadag, Sookyung Kim, Ugur Ozcelik, Ana Reula, Jobst Roehmel, Christine van Gogh, Panayiotis Yiallouros, Soeren Marian Zappe
Publikováno v:
BMJ Open, Vol 11, Iss 10 (2021)
Introduction Primary ciliary dyskinesia (PCD) is a rare, genetic, multiorgan disease with an estimated prevalence of 1 in 10 000. It affects mainly the upper and lower airways due to impaired mucociliary clearance. Almost all patients have sinonasal
Externí odkaz:
https://doaj.org/article/5e574ce429674f9a97c4b49e0130f59d
Autor:
Hannah Farley, Bruna Rubbo, Zuzanna Bukowy-Bieryllo, Mahmoud Fassad, Myrofora Goutaki, Katharine Harman, Claire Hogg, Claudia E. Kuehni, Susana Lopes, Kim G. Nielsen, Dominic P. Norris, Ana Reula, Nisreen Rumman, Amelia Shoemark, Hannah Wilkins, Agatha Wisse, Jane S. Lucas, June K. Marthin
Publikováno v:
BMC Proceedings, Vol 12, Iss S16, Pp 1-15 (2018)
Abstract Primary ciliary dyskinesia (PCD) is a chronic suppurative airways disease that is usually recessively inherited and has marked clinical phenotypic heterogeneity. Classic symptoms include neonatal respiratory distress, chronic rhinitis since
Externí odkaz:
https://doaj.org/article/af2d9c8b8e4d402d92c1f423fc75cbfa
Autor:
Manuel Mata PhD, Javier Zurriaga PhD, Lara Milian PhD, Ana Reula PhD, Miguel Armengot PhD, Amparo Ruiz-Sauri PhD, Carmen Carda PhD
Publikováno v:
Allergy & Rhinology, Vol 12 (2021)
Background Primary ciliary dyskinesia (PCD) is characterised by an imbalance in mucociliary clearance leading to chronic respiratory infections. Cilia length is considered to be a contributing factor in cilia movement. Recently, IFT46 protein has bee
Externí odkaz:
https://doaj.org/article/a9ceed264cc049c68b83952d104341e0
Autor:
Florian Halbeisen, Claire Hogg, Mikkel C. Alanin, Zuzanna Bukowy-Bieryllo, Francisco Dasi, Julie Duncan, Amanda Friend, Myrofora Goutaki, Claire Jackson, Victoria Keenan, Amanda Harris, Robert A. Hirst, Philipp Latzin, Gemma Marsh, Kim Nielsen, Dominic Norris, Daniel Pellicer, Ana Reula, Bruna Rubbo, Nisreen Rumman, Amelia Shoemark, Woolf T. Walker, Claudia E. Kuehni, Jane S. Lucas
Publikováno v:
BMC Proceedings, Vol 12, Iss S2, Pp 1-17 (2018)
Abstract Primary ciliary dyskinesia (PCD) is a rare heterogenous condition that causes progressive suppurative lung disease, chronic rhinosinusitis, chronic otitis media, infertility and abnormal situs. ‘Better Experimental Approaches to Treat Prim
Externí odkaz:
https://doaj.org/article/29ca8ce040c442819bc271f723d9c151
Autor:
Ana Reula, Javier Pitarch-Fabregat, Javier Milara, Julio Cortijo, Manuel Mata-Roig, Lara Milian, Miguel Armengot
Publikováno v:
Diagnostics, Vol 11, Iss 7, p 1301 (2021)
Primary ciliary dyskinesia (PCD) is a rare disease resulting from a defect in ciliary function that generates, among other issues, chronic upper and lower respiratory tract infections. European guidelines recommend studying ciliary function (pattern
Externí odkaz:
https://doaj.org/article/944b69d51a064056b0adcb838d986196
Autor:
Myrofora Goutaki, Yin Ting Lam, Mihaela Alexandru, Andreas Anagiotos, Miguel Armengot, Mieke Boon, Andrea Burgess, Nathalie Caversaccio, Suzanne Crowley, Sinan Ahmed D. Dheyauldeen, Nagehan Emiralioglu, Ela Erdem, Christine van Gogh, Onder Gunaydın, Eric G. Haarman, Amanda Harris, Isolde Hayn, Hasnaa Ismail-Koch, Bulent Karadag, Céline Kempeneers, Sookyung Kim, Natalie Lorent, Ugur Ozcelik, Charlotte Pioch, Anne-Lise ML Poirrier, Ana Reula, Jobst Roehmel, Panayiotis Yiallouros, Ali Cemal Yumusakhuylu, Jean-François Papon
ImportanceOtologic disease is common among people with primary ciliary dyskinesia, yet little is known about its spectrum and severity.ObjectiveWe characterized otologic disease among participants with primary ciliary dyskinesia using data from the E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08d84f4e3c430d96091142a88ace2132
https://doi.org/10.1101/2022.11.16.22282340
https://doi.org/10.1101/2022.11.16.22282340
