Phivos Ioannou
Nicosia, Cyprus
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
The CARMUCI Study Design: A Double-Blind, Cross-Over Sham-Controlled Trial of Indoor Air Purification in People With Cystic Fibrosis and Primary Ciliary Dyskinesia.
Journal: Pediatric pulmonology
Published: September 16, 2025
Co-segregation of the c.489+3A>G variant with p.Cys1400Ter pathogenic CFTR mutation in Cyprus: prevalence and clinical implications.
Journal: Orphanet journal of rare diseases
Published: December 18, 2024
Observational study of health utilities in adult primary ciliary dyskinesia patients: preliminary data on associations with molecular diagnosis, clinical phenotype and HRQOL measures.
Journal: Multidisciplinary respiratory medicine
Published: September 05, 2022
Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry.
Journal: Orphanet journal of rare diseases
Published: April 06, 2021
Health related quality of life in adult primary Ciliary dyskinesia patients in Cyprus: development and validation of the Greek version of the QOL-PCD questionnaire.
Journal: Health and quality of life outcomes
Published: September 21, 2019
Clinical features of primary ciliary dyskinesia in Cyprus with emphasis on lobectomized patients.
Journal: Respiratory medicine
Published: October 09, 2014
Apparent Homozygosity of p.Phe508del in CFTR due to a Large Gene Deletion of Exons 4-11.
Journal: Case reports in genetics
Published: November 22, 2013
Gender differences in objectively assessed physical activity in asthmatic and non-asthmatic children.
Journal: Pediatric pulmonology
Published: October 18, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026