Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Katarzyna Walicka-Serzysko"'
Autor:
Katarzyna Walicka-Serzysko, Magdalena Postek, Urszula Borawska-Kowalczyk, Katarzyna Szamotulska, Piotr Kwaśniewicz, Krystyna Polak, Ewa Mierzejewska, Dorota Sands, Magdalena Rutkowska
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-14 (2024)
Abstract Background The long-term consequences of prematurity are often not sufficiently recognized. To address this gap, a prospective cohort study, which is a continuation of the multicenter Polish study PREMATURITAS, was conducted, utilizing uniqu
Externí odkaz:
https://doaj.org/article/00300eb2f21440088ec5a7aa58714386
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
IntroductionIn cystic fibrosis (CF), pathological lung changes begin early in life. The technological progress currently gives many diagnostic possibilities. However, pulmonary function testing in children remains problematic.ObjectivesOur study aime
Externí odkaz:
https://doaj.org/article/ad8fd4526f9944afabfc4a0319dde597
Autor:
Dorota Sands, Katarzyna Walicka-Serzysko, Justyna Milczewska, Magdalena Postek, Natalia Jeneralska, Aleksandra Cichocka, Ewa Siedlecka, Urszula Borawska-Kowalczyk, Laurent Morin
Publikováno v:
Children, Vol 10, Iss 2, p 204 (2023)
Background: Cystic fibrosis (CF) patients require regular airway clearance therapy (ACT). The aim of this study was to evaluate homecare therapeutic effects of a new ACT (Simeox®) added to the optimal standard of care, including home chest physiothe
Externí odkaz:
https://doaj.org/article/5f434dab61e8497bbff3d9e0ce2952bc
Autor:
Dorota Sands, Justyna Milczewska, Katarzyna Walicka-Serzysko, Andrzej Pogorzelski, Szczepan Cofta, Wojciech Skorupa
Publikováno v:
Forum Zakażeń. 12:163-173
Przewlekła choroba oskrzelowo-płucna, której postęp spowodowany jest przewlekłymi zakażeniami, stanowi główną przyczynę hospitalizacji i śmierci osób chorych na mukowiscydozę. Wśród bakterii najczęściej powodujących przewlekłe zaka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::186030de2422b66edd684bd30d99ca4a
https://doi.org/10.15374/fz2021025
https://doi.org/10.15374/fz2021025
Autor:
Aurelie Hatton, Anne Bergougnoux, Katarzyna Zybert, Benoit Chevalier, Myriam Mesbahi, Jean Pierre Altéri, Katarzyna Walicka-Serzysko, Magdalena Postek, Magali Taulan-Cadars, Aleksander Edelman, Alexandre Hinzpeter, Mireille Claustres, Emmanuelle Girodon, Caroline Raynal, Isabelle Sermet-Gaudelus, Dorota Sands
Publikováno v:
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis, Elsevier, 2021, ⟨10.1016/j.jcf.2021.12.010⟩
Journal of Cystic Fibrosis, Elsevier, 2021, ⟨10.1016/j.jcf.2021.12.010⟩
Newborn screening for Cystic Fibrosis (CF) is associated with situations where the diagnosis of CF or CFTR related disorders (CFTR-RD) cannot be clearly ruled out.We report a case series of 23 children with unconclusive diagnosis after newborn screen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b889fca7a5e9bb08de2449d8ff7bad23
https://hal.archives-ouvertes.fr/hal-03503341/document
https://hal.archives-ouvertes.fr/hal-03503341/document
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 21
Journal of Clinical Medicine, Vol 10, Iss 4884, p 4884 (2021)
Volume 10
Issue 21
Journal of Clinical Medicine, Vol 10, Iss 4884, p 4884 (2021)
(1) Background: Pulmonary exacerbation (PEx) is one of the main factors affecting the quality of life and life expectancy in patients with cystic fibrosis (CF). Our study aimed to evaluate the change in selected pulmonary function parameters, includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa874a0a73ba52e572eeb7e5217f2750
Autor:
Dorotha Sands, Natalia Jeneralska, Magdalena Postek, Ewa Siedlecka, Justyna Milczewska, Katarzyna Walicka-Serzysko, Laurent Morin, Aleksandra Cichocka
Publikováno v:
Paediatric cystic fibrosis (CF).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ad303b841b87dba75d6d85f2b784000
https://doi.org/10.1183/13993003.congress-2021.pa3379
https://doi.org/10.1183/13993003.congress-2021.pa3379
Autor:
Justyna Milczewska, Ewa Mierzejewska, Katarzyna Walicka-Serzysko, Katarzyna Zacharczuk, Tomasz Wołkowicz, Dorota Sands, Monika Kwiatkowska
Publikováno v:
Pediatric Pulmonology. 55:161-168
Introduction Pseudomonas aeruginosa cross-infections are related to increased morbidity and mortality in cystic fibrosis (CF). Objectives The aim of the study was to evaluate the incidence of cross-infections with P. aeruginosa in children with CF. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1922a1264e855f09a610df416bab7341
https://doi.org/10.1002/ppul.24535
https://doi.org/10.1002/ppul.24535
Publikováno v:
Pediatric pulmonologyREFERENCES. 55(11)
Introduction Lung disease in cystic fibrosis (CF) begins early in life but the capabilities for detecting abnormalities of pulmonary dysfunction in children remain limited. Objective The study aimed to evaluate the early progression of lung function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e672ab16d2982e3e413b0d0b5e15936
https://pubmed.ncbi.nlm.nih.gov/32761970
https://pubmed.ncbi.nlm.nih.gov/32761970