Houyem Ouragini

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 18 publications

Mutation Spectrum of Hemoglobinopathies in Tunisia.

Mutation Spectrum of Hemoglobinopathies in Tunisia.

Journal: Human mutation

Published: November 28, 2025

Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia.

Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia.

Journal: International journal of neonatal screening

Published: August 29, 2025

Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in Tunisia.

Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in Tunisia.

Journal: International journal of molecular sciences

Published: February 02, 2025

PHINDaccess Hackathons for COVID-19 and Host-Pathogen Interaction: Lessons Learned and Recommendations for Low- and Middle-Income Countries.

PHINDaccess Hackathons for COVID-19 and Host-Pathogen Interaction: Lessons Learned and Recommendations for Low- and Middle-Income Countries.

Journal: BioMed research international

Published: April 15, 2023

Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach.

Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach.

Journal: Molecular syndromology

Published: November 03, 2022

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family.

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family.

Journal: Annals of clinical biochemistry

Published: October 10, 2022

Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn.

Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn.

Journal: American journal of perinatology

Published: February 21, 2022

Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.

Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.

Journal: American journal of perinatology

Published: December 29, 2020

First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby.

First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby.

Journal: Journal of pediatric hematology/oncology

Published: August 11, 2020

Clinical and genetic investigation of catecholaminergic polymorphic ventricular tachycardia in a consanguineous Tunisian family.

Clinical and genetic investigation of catecholaminergic polymorphic ventricular tachycardia in a consanguineous Tunisian family.

Journal: Acta cardiologica

Published: August 28, 2019

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Journal: Hemoglobin

Published: June 09, 2017

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.

Journal: Hematology (Amsterdam, Netherlands)

Published: November 22, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026