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Maria Gioulvanidou

Biographic Data

ID8254192
NAMEMaria Gioulvanidou
GIVEN NAMESMaria
FAMILY NAMEGioulvanidou
SIGNATUREGIOULVANIDOU M
AFFILIATIONSAristotle University of Thessaloniki
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2022
LATEST PUBLICATION YEAR2025
H-INDEX0
  • The Feasibility and Validity of Home Spirometry for People with Cystic Fibrosis

    Open Access•Athina Sopiadou, Maria Gioulvanidou et al.•ARTICLE•Children•2025

    Background/Objectives : Home spirometry allows people with cystic fibrosis (CF) to monitor their lung function from home. However, there are concerns about its feasibility and validity compared to traditional clinic spirometry. The aim of this study was to evaluate the feasibility and validity of telehealth spirometry for patients with CF living in a regional setting. Methods : This retrospective study included forty-eight people with cystic fibr…

  • Physical Activity and Quality of Life among Patients with Cystic Fibrosis

    Open Access•Stavros Giannakoulakos, Maria Gioulvanidou et al.•ARTICLE•Children•2022

    The children with CF showed satisfactory PA levels, which positively correlated to their QoL. More research is needed on the effect of increased levels of habitual physical activity to establish the decline in pulmonary function among pwCF

No prominent works on this page.

  • Physical Activity and Quality of Life among Patients with Cystic Fibrosis

    Open Access•Stavros Giannakoulakos, Maria Gioulvanidou et al.•ARTICLE•Children•2022

    The children with CF showed satisfactory PA levels, which positively correlated to their QoL. More research is needed on the effect of increased levels of habitual physical activity to establish the decline in pulmonary function among pwCF

  • The Feasibility and Validity of Home Spirometry for People with Cystic Fibrosis

    Open Access•Athina Sopiadou, Maria Gioulvanidou et al.•ARTICLE•Children•2025

    Background/Objectives : Home spirometry allows people with cystic fibrosis (CF) to monitor their lung function from home. However, there are concerns about its feasibility and validity compared to traditional clinic spirometry. The aim of this study was to evaluate the feasibility and validity of telehealth spirometry for patients with CF living in a regional setting. Methods : This retrospective study included forty-eight people with cystic fibr…

Asthma (2 works) · Cystic fibrosis (2 works) · Cystic Fibrosis Research Advances (2 works) · Internal Medicine (2 works) · Lung (2 works) · Lung function (2 works) · Medicine (2 works) · Physical therapy (2 works) · Spirometry (2 works) · Child Nutrition and Feeding Issues (1 work)

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