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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.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.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.Pharmaceutical Biology|May 31, 2022
Flaxseed extract reduces tissue accumulation and enhances urinary excretion of chondroitin sulphate in the rat: a possible new path in substrate reduction therapy for mucopolysaccharidosisSabir Es-Said, Karima Lafhal, Abdelaati Elkhiat, et al.Frontiers in Cell and Developmental Biology|March 12, 2026
Prenatal alcohol exposure induces anxiety and depressive-like behaviors with deficits in growth and food intake in miceKamal Smimih, Bilal El-Mansoury, Mohamed Marghich, 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.Acta Neurobiologiae Experimentalis|July 26, 2023
Hyperammonemia induced gut microbiota dysbiosis and motor coordination disturbances in mice: new insight into gut‑brain axis involvement in hepatic encephalopathyAimrane Abdelmohcine, Souad El Amine, Karima Warda, 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.Pageof 2