Hassen Kamoun
Sfax, Tunisia
Last Updated: 09/26/2026
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Found 56 publications
Abstracts Association Tunisienne de Médecine Néonatale (ATMN).
Journal: La Tunisie medicale
Published: December 31, 2025
Genetic investigation of a Tunisian family with Lynch syndrome: a case report.
Journal: Frontiers in oncology
Published: September 05, 2025
Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohort.
Journal: Annales d'endocrinologie
Published: April 09, 2025
Genetic profiling of inherited colorectal cancer syndromes in Tunisian patients.
Journal: PloS one
Published: March 08, 2025
Gardner syndrome in a Tunisian family: Identification of a rare APC mutation through targeted NGS.
Journal: Gene
Published: July 18, 2024
Primary adrenal insufficiency in children excluding congenital adrenal hyperplasia: insights from 33-year single-center experience in Tunisia.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: February 06, 2024
Genetic insights into fetal kidney development: Variants in HNF1A and PKHD1 genes.
Journal: Gene
Published: February 03, 2024
Case report: Compound heterozygous variants detected by next-generation sequencing in a Tunisian child with ataxia-telangiectasia.
Journal: Frontiers in neurology
Published: November 24, 2023
Strategies for diagnosis and management of CMMRD in low-resource countries: report of a Tunisian family.
Journal: Familial cancer
Published: November 17, 2023
Genome Tunisia Project: paving the way for precision medicine in North Africa.
Journal: Genome medicine
Published: May 02, 2023
Update meta-analysis from biomedical literature about MTHFR'polymorphisms and the CML' risk.
Journal: La Tunisie medicale
Published: September 26, 2022
Last Updated: 09/26/2026