Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Dorota Sands"'
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
Autor:
Anne Munck, Kevin W. Southern, Jared Murphy, Karin M. de Winter-de Groot, Silvia Gartner, Bülent Karadag, Nataliya Kashirskaya, Barry Linnane, Marijke Proesmans, Dorota Sands, Olaf Sommerburg, Carlo Castellani, Jürg Barben
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 4, p 65 (2023)
Repeated European surveys of newborn bloodspot screening (NBS) have shown varied strategies for collecting missed cases, and information on data collection differs among countries/regions, hampering data comparison. The ECFS Neonatal Screening Workin
Externí odkaz:
https://doaj.org/article/b5f12209c8cb410c8b86b75d266ab8ce
Autor:
Katarzyna Zybert, Urszula Borawska-Kowalczyk, Lukasz Wozniacki, Malwina Dawidziuk, Mariusz Ołtarzewski, Dorota Sands
Publikováno v:
Jornal de Pediatria, Vol 98, Iss 4, Pp 419-424 (2022)
Objective: To present signs and symptoms and clinical course in cystic fibrosis patients with false-negative newborn screening (CF NBS). Materials and methods: All children presented in this paper were covered by CF NBS. The group of 1.869.246 newbor
Externí odkaz:
https://doaj.org/article/6b1e6c8eb58747399ac5347c54ad51c5
Autor:
Grażyna Dykowska, Ewa Śmigrocka, Urszula Borawska-Kowalczyk, Dorota Sands, Zofia Sienkiewicz, Anna Leńczuk-Gruba, Damian Gorczyca, Mariola Głowacka
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 16, p 5214 (2023)
Parental perspective on the health, safety, and quality of life in children and adolescents with cystic fibrosis (CF). Aim of the study: Assessment of the impact of a chronic disease such as cystic fibrosis (CF) on the quality of life and safety of c
Externí odkaz:
https://doaj.org/article/6562b54798a94f36bf9e680c0a0ae8b7
Autor:
Katarzyna Walicka-Serzysko, Magdalena Postek, Urszula Borawska-Kowalczyk, Justyna Milczewska, Dorota Sands
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 14, p 4735 (2023)
Background: Properly evaluating respiratory system dysfunction is essential in children with cystic fibrosis (CF). This prospective study aimed to assess the course of early lung disease based on multiple breath nitrogen washout (MBNW), impulse oscil
Externí odkaz:
https://doaj.org/article/fb0bb32ca7ce458d952c5a28b19e4a33
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 9, p 3086 (2023)
With the increasing longevity of cystic fibrosis (CF), there is a growing need to minimise exposure to ionising radiation in patients who undergo regular imaging tests while monitoring the course of the lung disease. This study aimed to define the ro
Externí odkaz:
https://doaj.org/article/1debdcb753ee4e289759430648089a03
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
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
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Cystic fibrosis (CF) is the most common, life-threatening, autosomal-recessive disorder among Caucasians. To date, approximately 2000 mutations in the CFTR gene have been reported. Some of these mutations are very rare, and some r
Externí odkaz:
https://doaj.org/article/8d1f9ceb841a4c3c9dedac08b3821fbd
Autor:
Karolina Anna Mielko, Sławomir Jan Jabłoński, Łukasz Pruss, Justyna Milczewska, Dorota Sands, Marcin Łukaszewicz, Piotr Młynarz
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 19, p 10820 (2021)
Pseudomonas aeruginosa is a common human pathogen belonging to the ESKAPE group. The multidrug resistance of bacteria is a considerable problem in treating patients and may lead to increased morbidity and mortality rate. The natural resistance in the
Externí odkaz:
https://doaj.org/article/d027bd2a2a334197b2073cb4ae19ab5e