Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Bruna Rubbo"'
Autor:
Renate Kos, Myrofora Goutaki, Helene E. Kobbernagel, Bruna Rubbo, Amelia Shoemark, Stefano Aliberti, Josje Altenburg, Pinelopi Anagnostopoulou, Rodrigo A. Athanazio, Nicole Beydon, Sharon D. Dell, Nagehan Emiralioglu, Thomas W. Ferkol, Michael R. Loebinger, Natalie Lorent, Bernard Maître, June Marthin, Lucy C. Morgan, Kim G. Nielsen, Felix C. Ringshausen, Michal Shteinberg, Harm A.W.M. Tiddens, Anke H. Maitland-Van der Zee, James D. Chalmers, Jane S.A. Lucas, Eric G. Haarman
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Background Consistent use of reliable and clinically appropriate outcome measures is a priority for clinical trials, with clear definitions to allow comparability. We aimed to develop a core outcome set (COS) for pulmonary disease interventions in pr
Externí odkaz:
https://doaj.org/article/206a1713eedc40ba92a771037176fcd8
Autor:
Chiara Dall’Ora, Bruna Rubbo, Christina Saville, Lesley Turner, Jane Ball, Cheska Ball, Peter Griffiths
Publikováno v:
Human Resources for Health, Vol 21, Iss 1, Pp 1-17 (2023)
Abstract Objectives Health systems worldwide are faced with the challenge of adequately staffing their hospital services. Much of the current research and subsequent policy has been focusing on nurse staffing and minimum ratios to ensure quality and
Externí odkaz:
https://doaj.org/article/ed85be2c1a224fc69576d8ce57527265
Autor:
Mihaela Alexandru, Raphaël Veil, Bruna Rubbo, Myrofora Goutaki, Sookyung Kim, Yin Ting Lam, Jérôme Nevoux, Jane S. Lucas, Jean-François Papon
Publikováno v:
European Respiratory Review, Vol 32, Iss 169 (2023)
Background Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by pulmonary, otological and sino-nasal manifestations. Well-defined clinical outcome measures are needed in such rare diseases research to improve follow-up and tre
Externí odkaz:
https://doaj.org/article/ed6bed3cdcb24ebc8519e9a6e1b93913
Autor:
Peter Griffiths, Chiara Dall'Ora, Jeremy Jones, Bruna Rubbo, Jane Ball, David Culliford, Christina Saville, Lesley Turner
Publikováno v:
BMJ Open, Vol 13, Iss 5 (2023)
Objectives Examine the association between multiple clinical staff levels and case-mix adjusted patient mortality in English hospitals. Most studies investigating the association between hospital staffing levels and mortality have focused on single p
Externí odkaz:
https://doaj.org/article/b091554381d64fa8974d8fe4fa5a7ecc
Autor:
Nisreen Rumman, Mahmoud R. Fassad, Corine Driessens, Patricia Goggin, Nader Abdelrahman, Adel Adwan, Mutaz Albakri, Jagrati Chopra, Regan Doherty, Bishara Fashho, Grace M. Freke, Abdallah Hasaballah, Claire L. Jackson, Mai A. Mohamed, Reda Abu Nema, Mitali P. Patel, Reuben J. Pengelly, Ahmad Qaaqour, Bruna Rubbo, N. Simon Thomas, James Thompson, Woolf T. Walker, Gabrielle Wheway, Hannah M. Mitchison, Jane S. Lucas
Publikováno v:
ERJ Open Research, Vol 9, Iss 2 (2023)
Background Diagnostic testing for primary ciliary dyskinesia (PCD) started in 2013 in Palestine. We aimed to describe the diagnostic, genetic and clinical spectrum of the Palestinian PCD population. Methods Individuals with symptoms suggestive of PCD
Externí odkaz:
https://doaj.org/article/f2c51f09226b40409f9747ca8c6802ba
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:
Florian Gahleitner, James Thompson, Claire L. Jackson, Jana F. Hueppe, Laura Behan, Eleonora Dehlink, Myrofora Goutaki, Florian Halbeisen, Ana Paula L. Queiroz, Guillaume Thouvenin, Claudia E. Kuehni, Philipp Latzin, Jane S. Lucas, Bruna Rubbo
Publikováno v:
ERJ Open Research, Vol 7, Iss 4 (2021)
Objectives Disease-specific, well-defined and validated clinical outcome measures are essential in designing research studies. Poorly defined outcome measures hamper pooling of data and comparisons between studies. We aimed to identify and describe p
Externí odkaz:
https://doaj.org/article/ce34efca1d914674ae85924056fb2ce0
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:
Myrofora Goutaki, Jean-François Papon, Mieke Boon, Carmen Casaulta, Ernst Eber, Estelle Escudier, Florian S. Halbeisen, Amanda Harris, Claire Hogg, Isabelle Honore, Andreas Jung, Bulent Karadag, Cordula Koerner-Rettberg, Marie Legendre, Bernard Maitre, Kim G. Nielsen, Bruna Rubbo, Nisreen Rumman, Lynne Schofield, Amelia Shoemark, Guillaume Thouvenin, Hannah Willkins, Jane S. Lucas, Claudia E. Kuehni
Publikováno v:
ERJ Open Research, Vol 6, Iss 1 (2020)
Clinical data on primary ciliary dyskinesia (PCD) are limited, heterogeneous and mostly derived from retrospective chart reviews, leading to missing data and unreliable symptoms and results of physical examinations. We need standardised prospective d
Externí odkaz:
https://doaj.org/article/c2d4bc651d864dd7bfd06d0e99f42061
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