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Jolanta Wlizło

Datos Biográficos

ID128819
NOMBREJolanta Wlizło
NOMBRESJolanta
APELLIDOWlizło
FIRMAWLIZŁO J
AFILIACIONESPoznan University of Medical Sciences
VERIFICADONo
TOTAL DE OBRAS2
TOTAL DE CITAS0
OBRAS COMO AUTOR2
OBRAS COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2020
AÑO MÁS RECIENTE DE PUBLICACIÓN2021
ÍNDICE H0
  • 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•Referencias: 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 …

Sin obras prominentes en esta página.

  • 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•Referencias: 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 obras) · Cystic fibrosis (2 obras) · Cystic Fibrosis Research Advances (2 obras) · Gastroenterology (2 obras) · Internal Medicine (2 obras) · Medicine (2 obras) · Bacterial biofilms and quorum sensing (1 obra) · Bioelectrical impedance analysis (1 obra) · Biological Research and Disease Studies (1 obra) · Biology (1 obra)

Ethnos_APP • Proyecto Open Source • Licencia MIT • Frontend v2.0.0 • Privacidad y Cookies • Documentación de la API: api.ethnos.app/docs • Código de la API: GitHub • DOI: 10.5281/zenodo.17049435 • Código del Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae