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Methods in Molecular Biology (Clifton, N.J.)|January 20, 2023
Urinary Glycosaminoglycans: Characterization and QuantificationNaima Fdil, Es-Said Sabir
Molecular Biology Reports|December 13, 2025
Identification of a novel nonsense mutation in the AGL gene in glycogen storage disease type IIIa: first genetically confirmed case report from MoroccoMaroua Jakani, Imane Assiri, Sana El Foutat, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 2, 2020
Usefulness of urinary glycosaminoglycans assay for a mucopolysaccharidosis-specific screeningEs-Said Sabir, Karima Lafhal, Aicha Ezoubeiri, et al.
Analytical Biochemistry|May 21, 2026
Novel HEXB Variant and First Evidence of Urinary Gb4 Isoforms in Sandhoff Disease: Biochemical and Bioinformatic Characterization in Two Moroccan FamiliesMiloud Hammoud, Alice M S Rodrigues, Imane Assiri, et al.
Carbohydrate Research|November 2, 2020
Update of a colorimetric method for quantitative determination of galactose in blood samples: A simple and rapid method for the early detection of inherited metabolic diseasesKarima Lafhal, Es-Said Sabir, Mouna Cheggour, et al.
Clinical Laboratory|March 13, 2020
Implementation of an Affordable Method for MPS Diagnosis from Urine Screening to Enzymatic Confirmation: Results of a Pilot Study in MoroccoNaima Fdil, Es-Said Sabir, Aicha Ezoubeiri, et al.
Molecular Genetics and Metabolism Reports|June 16, 2023
Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patientsKarima Lafhal, Es-Said Sabir, Abdelmalek Hakmaoui, et al.
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