Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Joanna Goździk-Spychalska

Biographic Data

ID128815
NAMEJoanna Goździk-Spychalska
GIVEN NAMESJoanna
FAMILY NAMEGoździk-Spychalska
SIGNATUREGOŹDZIK-SPYCHALSKA J
AFFILIATIONSPoznan University of Medical Sciences
ORCID0000-0002-4518-7070
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
AUTHOR COUNT2
EDITOR COUNT0
FIRST PUBLICATION YEAR2020
LATEST PUBLICATION YEAR2021
H-INDEX0
  • The determinants of survival among adults with cystic fibrosis-a cohort study

    Open Access•Magdalena Durda‐masny, Magdalena Durda-Masny et al.•ARTICLE•Journal of PHYSIOLOGICAL…•2021•References: 29

    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 infection development by Pseudomonas aeruginosa. The study aimed to evaluate the relationship between the severity of mutation, nutritional status, lung function, and Pseudomonas aeruginosa prevalence …

  • Body composition and lung function in adults with Cystic Fibrosis

    Open Access•Aleksandra John, Joanna Goździk-Spychalska et al.•ARTICLE•Anthropological Review•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) the relationship between lung function and body composition in CF patients. We studied 37 CF patients aged 19 to 51 years, and 41 healthy non-CF volunteers. Nutritional status was evaluated based on …

No prominent works on this page.

  • Body composition and lung function in adults with Cystic Fibrosis

    Open Access•Aleksandra John, Joanna Goździk-Spychalska et al.•ARTICLE•Anthropological Review•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) the relationship between lung function and body composition in CF patients. We studied 37 CF patients aged 19 to 51 years, and 41 healthy non-CF volunteers. Nutritional status was evaluated based on …

  • The determinants of survival among adults with cystic fibrosis-a cohort study

    Open Access•Magdalena Durda‐masny, Magdalena Durda-Masny et al.•ARTICLE•Journal of PHYSIOLOGICAL…•2021•References: 29

    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 infection development by Pseudomonas aeruginosa. The study aimed to evaluate the relationship between the severity of mutation, nutritional status, lung function, and Pseudomonas aeruginosa prevalence …

Body mass index (2 works) · Cystic fibrosis (2 works) · Cystic Fibrosis Research Advances (2 works) · Gastroenterology (2 works) · Internal Medicine (2 works) · Medicine (2 works) · Bacterial biofilms and quorum sensing (1 work) · Bioelectrical impedance analysis (1 work) · Biological Research and Disease Studies (1 work) · Biology (1 work)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae