Samia Hamouda

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 23 publications

Characterising cystic fibrosis in African populations: a scoping review protocol on phenotype, diagnosis, genetics and barriers to care.

Characterising cystic fibrosis in African populations: a scoping review protocol on phenotype, diagnosis, genetics and barriers to care.

Journal: BMJ open

Published: February 10, 2026

Standards for the care of people with cystic fibrosis (CF); Planning for a longer life.

Standards for the care of people with cystic fibrosis (CF); Planning for a longer life.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: February 12, 2024

A gain-of-function mutation in zinc cluster transcription factor Rob1 drives Candida albicans adaptive growth in the cystic fibrosis lung environment.

A gain-of-function mutation in zinc cluster transcription factor Rob1 drives Candida albicans adaptive growth in the cystic fibrosis lung environment.

Journal: PLoS pathogens

Published: November 29, 2023

Characteristics and predictors of outcome in children with severe acute bronchiolitis: A 10-yearexperience.

Characteristics and predictors of outcome in children with severe acute bronchiolitis: A 10-yearexperience.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: January 11, 2023

A case report of inherited surfactant protein deficiency: unknown cause of diffuse infiltrative diseases in Tunisia.

A case report of inherited surfactant protein deficiency: unknown cause of diffuse infiltrative diseases in Tunisia.

Journal: La Tunisie medicale

Published: December 26, 2022

Instability of Mature ABCA3 Protein: Toward a New Classification of ABCA3 Mutations?

Instability of Mature ABCA3 Protein: Toward a New Classification of ABCA3 Mutations?

Journal: American journal of respiratory cell and molecular biology

Published: November 01, 2022

Variable Expression of Lung Disease Due to a Novel Homozygous ABCA3 Variant.

Variable Expression of Lung Disease Due to a Novel Homozygous ABCA3 Variant.

Journal: Pediatric allergy, immunology, and pulmonology

Published: September 19, 2022

Tracheal Hemangioma: A Rare Cause of Hemoptysis in Children.

Tracheal Hemangioma: A Rare Cause of Hemoptysis in Children.

Journal: Ear, nose, & throat journal

Published: July 07, 2022

Up-to-date incidence and initial characteristics of cystic fibrosis in Tunisia.

Up-to-date incidence and initial characteristics of cystic fibrosis in Tunisia.

Journal: Pediatric pulmonology

Published: May 19, 2022

Congenital surfactant protein B (SP-B) deficiency: a case report.

Congenital surfactant protein B (SP-B) deficiency: a case report.

Journal: The Pan African medical journal

Published: May 05, 2022

Impact of illness on mothers of children with cystic fibrosis in Tunisia: A qualitative interview study: Impact of cystic fibrosis on Tunisian mothers.

Impact of illness on mothers of children with cystic fibrosis in Tunisia: A qualitative interview study: Impact of cystic fibrosis on Tunisian mothers.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: October 21, 2021

Difficulties in the treatment of an infant survivor with inherited surfactant protein-B deficiency in Tunisia.

Difficulties in the treatment of an infant survivor with inherited surfactant protein-B deficiency in Tunisia.

Journal: Annals of thoracic medicine

Published: October 03, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026