19 Apr 2026
Clinical and molecular spectrum of primary hyperoxaluria type 1 in Tunisia: pediatric presentation and minimum observed prevalencePublisher sitePediatric Nephrology, Kidney Stones and Urolithiasis Treatments
UniversitiesMédiha Trabelsi
Active, last published 2026
Médiha
Trabelsi
Scholar“Research profile drawn from open scholarly records.”
Hôpital Charles-Nicolle
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01 · About the work
What I study
research summary for Médiha Trabelsi will appear here once their profile is updated.
02 · Reach
Publication output and reach
Médiha's work has been cited 14 times across 4 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
04 · Where I am
Affiliations
Affiliation on published researchHôpital Charles-NicolleDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
11 works1 Jan 2026Open access
First Detection of 1p36 Deletion by Whole‐Exome Sequencing in a Tunisian PatientPublisher siteBirth Defects Research, Genomic variations and chromosomal abnormalities
8 Dec 2025Open access
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosityPublisher siteProceedings of the National Academy of Sciences, Hearing, Cochlea, Tinnitus, Genetics
3 Dec 2024Open access
Interstitial 11q deletion in a patient with Sprengel’s deformity: a case report and review of the literaturePublisher siteMolecular Cytogenetics, Genomic variations and chromosomal abnormalities
1 Oct 2024Open access1cites
Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent <scp>POLR3A</scp> Mutation in Six Unrelated Tunisian FamiliesPublisher siteMolecular Genetics & Genomic Medicine, RNA regulation and disease
26 Aug 2024Open access10cites
Genome Tunisia Project: paving the way for precision medicine in North AfricaPublisher siteGenome Medicine, Genomics and Rare Diseases
14 Aug 2024
Genetic study of Alport syndrome in TunisiaPublisher sitePediatric Nephrology, Cell Adhesion Molecules Research
25 Jun 2024Open access1cites
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthPublisher siteFrontiers in Genetics, Hearing, Cochlea, Tinnitus, Genetics
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