Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Catherine Kruljac"'
Autor:
Eva S.L. Pedersen, Myrofora Goutaki, Leonie D. Schreck, Bernhard Rindlisbacher, Lucy Dixon, Jane S. Lucas, Claudia E. Kuehni, the COVID-PCD patient advisory group, Sara Bellu, Isabelle Cizeau, Katie Dexter, Trini López Fernández, Susanne Grieder, Catherine Kruljac, Michele Manion, Hansruedi Silberschmidt, Emilie Wattellier
Publikováno v:
ERJ Open Research, Vol 10, Iss 5 (2024)
Externí odkaz:
https://doaj.org/article/32cbfbcba1ea4c50a691410254657f66
Autor:
Leonie Daria Schreck, Eva Sophie Lunde Pedersen, Isabelle Cizeau, Loretta Müller, Catherine Kruljac, Jane S Lucas, Myrofora Goutaki, COVID-PCD patient advisory group, Claudia E Kuehni
Publikováno v:
PLOS Global Public Health, Vol 3, Iss 9, p e0001522 (2023)
Diagnostic tests are important in primary ciliary dyskinesia (PCD), a rare disease, to confirm the diagnosis and characterize the disease. We compared diagnostic tests for PCD between countries worldwide, assessed whether people with PCD recall their
Externí odkaz:
https://doaj.org/article/8aea4f457ae74805968f0d03250d0dba
Autor:
Anne B Chang, Keith Grimwood, Yuejen Zhao, Gabrielle B McCallum, Peter S Morris, Andre Schultz, Emma L Duncan, Aideen M McInerney-Leo, Stephanie T Yerkovich, Steven M McPhail, Danielle Wurzel, Julie M Marchant, Paul J Leo, Anne L Cook, Lucy C Morgan, Margaret S McElrea, Lesley Versteegh, Mark D Chatfield, Catherine Kruljac, Heidi C Smith-Vaughan, Hannah O’Farrell, Sabine Fletcher, Heather D'Antoine, Enna Stroil-Salama, Phil J Robinson
Publikováno v:
BMJ Open Respiratory Research, Vol 9, Iss 1 (2022)
Introduction Primary ciliary dyskinesia (PCD) is a rare, progressive, inherited ciliopathic disorder, which is incurable and frequently complicated by the development of bronchiectasis. There are few randomised controlled trials (RCTs) involving chil
Externí odkaz:
https://doaj.org/article/4c36499478d34d1899fd92d8874d598c
Autor:
Eva S. L. Pedersen, Eugenie N. R. Collaud, Rebeca Mozun, Katie Dexter, Catherine Kruljac, Hansruedi Silberschmidt, Jane S. Lucas, COVID-PCD patient advisory group, Myrofora Goutaki, Claudia E. Kuehni, Rindlisbacher Bernhard, Kruljac Catherine, Copeland Fiona, Silberschmidt Hansruedi, Dexter Katie, Dixon Lucy, Manion Michelle, Bellu Sara, Grieder Susanne
Publikováno v:
International Journal of Public Health, Vol 66 (2021)
Objectives: Primary ciliary dyskinesia (PCD) is a rare genetic disease that causes recurrent respiratory infections. People with PCD may be at high risk of severe COVID-19 and protection against SARS-CoV-2 is therefore important. We studied facemask
Externí odkaz:
https://doaj.org/article/6118527b1beb4ce9885cc730510d698b
Autor:
Rebeca Mozun, Myrofora Goutaki, Hansruedi Silberschmidt, Claudia E. Kuehni, Katie Dexter, Jane S. Lucas, Eva S.L. Pedersen, Catherine Kruljac, Eugénie N.R. Collaud
Publikováno v:
Paediatric respiratory epidemiology.
Autor:
Eugénie N.R. Collaud, Hansruedi Silberschmidt, Claudia E. Kuehni, Rebeca Mozun, Jane S. Lucas, Myrofora Goutaki, Catherine Kruljac, Eva S.L. Pedersen, Katie Dexter
BackgroundFacemasks help prevent transmission of SARS-CoV-2 and are particularly important for people with chronic respiratory disease such as primary ciliary dyskinesia (PCD). We studied the usage of facemasks and its consequences among people with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bd40380d96b25f839810f094c0121cc
https://doi.org/10.1101/2021.04.13.21255393
https://doi.org/10.1101/2021.04.13.21255393