Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Wojciech Czaiński"'
Autor:
Magdalena Durda-Masny, Joanna Goździk-Spychalska, Aleksandra John, Wojciech Czaiński, Weronika Stróżewska, Natalia Pawłowska, Jolanta Wlizło, Halina Batura-Gabryel, Anita Szwed
Publikováno v:
Journal of Physiological Anthropology, Vol 40, Iss 1, Pp 1-9 (2021)
Abstract Background Cystic fibrosis (CF) is one of the most common autosomal recessive diseases. Factors contributing to disease exacerbations and survival rate of CF patients are type of mutation in the CFTR gene, poor nutritional status, lung failu
Externí odkaz:
https://doaj.org/article/a3b89a401219428aa2292820666691b0
Autor:
Jolanta Wlizło, Anita Szwed, Joanna Goździk-Spychalska, Aleksandra John, Halina Batura-Gabryel, Wojciech Czaiński, Natalia Pawłowska, Magdalena Durda-Masny, Weronika Stróżewska
Publikováno v:
Journal of Physiological Anthropology, Vol 40, Iss 1, Pp 1-9 (2021)
Journal of Physiological Anthropology
Journal of Physiological Anthropology
Background Cystic fibrosis (CF) is one of the most common autosomal recessive diseases. Factors contributing to disease exacerbations and survival rate of CF patients are type of mutation in the CFTR gene, poor nutritional status, lung failure, and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::014841ea0a3904e3023df9909e9e7257
https://doaj.org/article/a3b89a401219428aa2292820666691b0
https://doaj.org/article/a3b89a401219428aa2292820666691b0
Autor:
Wojciech Czaiński, Magdalena Durda-Masny, Halina Batura-Gabryel, Marta Gębala, Aleksandra John, Anita Szwed, Joanna Goździk-Spychalska, Jolanta Wlizło
Publikováno v:
Anthropological Review, Vol 83, Iss 3, Pp 239-250 (2020)
The study aimed to assess: (1) differences in nutritional status and lung function between CF patients and the control group; (2) differences in body composition and lung function between groups of patients with CF designated by type of mutation; (3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09d36896980e4064b5a6bfb6ef02d482
https://doi.org/10.2478/anre-2020-0021
https://doi.org/10.2478/anre-2020-0021
Autor:
Magdalena Durda-Masny, Joanna Gozdzik-Spychalska, Wojciech Czaiński, Anita Szwed, Jolanta Wlizło, Halina Batura-Gabryel, Aleksandra John, Natalia Pawłowska
Background: Cystic fibrosis (CF) is one of the most common autosomal recessive disease, and the type of mutation is recognized as one of the most important factors determining the survival rate. Factors contributing to disease exacerbations, and surv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a9bfaedc5f96e64f56cc83cfffadf65
https://doi.org/10.21203/rs.3.rs-131715/v1
https://doi.org/10.21203/rs.3.rs-131715/v1
Autor:
Halina Batura-Gabryel, Magdalena Durda-Masny, Wojciech Czaiński, Natalia Pawłowska, Joanna Goździk-Spychalska, Jolanta Wlizło, Anita Szwed, Aleksandra John
Publikováno v:
Nutrition. 89:111221
The aim of this study was to describe the relationship between the prevalence of Pseudomonas aeruginosa (PA) and lung function, as well as the nutritional status and type of gene mutation in adult patients with cystic fibrosis (CF).This cross-section
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9503d76904965c3b943e47545563c5f
https://doi.org/10.1016/j.nut.2021.111221
https://doi.org/10.1016/j.nut.2021.111221