1 Nov 2025
Bone involvement in Gaucher disease: Data from a North African registryPublisher siteReumatología Clínica (English Edition), Lysosomal Storage Disorders Research
Active, last published 2026
In lysosomal storage disorders research
Amel Ben
Chehida
Scholar“Research focused on Lysosomal Storage Disorders Research and adjacent fields.”
University of Tunis El Manar
Tunisia
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01 · About the work
What I study
mel Ben Chehida is a researcher working on Lysosomal Storage Disorders Research. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Amel's work has been cited 413 times across 2 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Lysosomal Storage Disorders Research×19Metabolism and Genetic Disorders×17Glycogen Storage Diseases and Myoclonus×10Carbohydrate Chemistry and Synthesis×7Mitochondrial Function and Pathology×6
04 · Where I am
Affiliations
Affiliation on published researchTunis University, TunisiaDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
7 works18 Oct 2025
Bone involvement in Gaucher disease: Data from a North African registryPublisher siteReumatología Clínica, Lysosomal Storage Disorders Research
24 Feb 2025Open access2cites
Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel <i>ROGDI</i> Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz SyndromePublisher siteClinical Genetics, RNA Research and Splicing
22 Feb 2025Open access
Dihydrolipoamide dehydrogenase deficiency in two unrelated Tunisian childrenPublisher siteBMC Pediatrics, Biochemical Acid Research Studies
18 Dec 20232cites
Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low‐GGT intrahepatic cholestasis: Genetic diagnosis and genotype–phenotype correlation assessmentPublisher siteAnnals of Human Genetics, Drug Transport and Resistance Mechanisms
1 Jul 2023Open access1cites
A Case of Infantile Cataract and Neonatal HypoglycemiaPublisher siteJournal of Current Ophthalmology, Intraocular Surgery and Lenses
28 Apr 2023Open access1cites
Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1bPublisher siteDiabetology & Metabolic Syndrome, Glycogen Storage Diseases and Myoclonus
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