Sondess Fredj-Hadj

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 30 publications

IL-10 promoter polymorphisms (-1082G > A,-819C > Tand - 592 C > A) and pediatric asthma susceptibility in a Mauritanian population.

IL-10 promoter polymorphisms (-1082G > A,-819C > Tand - 592 C > A) and pediatric asthma susceptibility in a Mauritanian population.

Journal: The Journal of asthma : official journal of the Association for the Care of Asthma

Published: July 06, 2026

Inflammatory Biomarkers in Sickle Cell Disease: Understanding Their Role in Predicting the Disease-Related Complications.

Inflammatory Biomarkers in Sickle Cell Disease: Understanding Their Role in Predicting the Disease-Related Complications.

Journal: Hemoglobin

Published: April 14, 2026

Glucose-6-phosphate dehydrogenase activity and genetic variants in tunisian diabetic populations: A case-control study.

Glucose-6-phosphate dehydrogenase activity and genetic variants in tunisian diabetic populations: A case-control study.

Journal: Journal of the National Medical Association

Published: January 12, 2026

Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency.

Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency.

Journal: The journal of applied laboratory medicine

Published: August 25, 2025

Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia.

Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia.

Journal: Annals of hematology

Published: August 15, 2025

The MNS blood group system in Tunisian blood donors: common and rare alleles.

The MNS blood group system in Tunisian blood donors: common and rare alleles.

Journal: Molecular biology reports

Published: February 11, 2025

Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study.

Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study.

Journal: Heliyon

Published: July 16, 2024

Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches.

Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches.

Journal: Molecular genetics and genomics : MGG

Published: February 09, 2024

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

Journal: Molecular genetics & genomic medicine

Published: July 22, 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

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.

Journal: Molecular biology reports

Published: February 22, 2021

Association analysis of the surfactant protein-C gene to childhood asthma.

Association analysis of the surfactant protein-C gene to childhood asthma.

Journal: The Journal of asthma : official journal of the Association for the Care of Asthma

Published: September 23, 2020

Showing 1-12 of 30

Last Updated: 09/26/2026