Dorra Chaouachi
Tunis, 1002, Tunisia
Last Updated: 09/26/2026
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Found 20 publications
Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia.
Journal: International journal of neonatal screening
Published: August 29, 2025
Circulating Erythrocyte- and Endothelial-Derived Microvesicles as Biomarkers of Hemolysis and Clinical Severity in Sickle Cell Disease.
Journal: Journal of cellular and molecular medicine
Published: July 29, 2025
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
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
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Published: February 02, 2021
Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency.
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Published: January 15, 2021
Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.
Journal: American journal of perinatology
Published: December 29, 2020
Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.
Journal: European journal of medical genetics
Published: March 01, 2020
New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level.
Journal: Journal of pediatric hematology/oncology
Published: November 06, 2019
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.
Journal: Hematology (Amsterdam, Netherlands)
Published: November 22, 2016
Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene.
Journal: International journal of laboratory hematology
Published: August 01, 2016
Last Updated: 09/26/2026