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Imane Assiri

Observed name: I. Assiri
Observed institution: Cadi Ayyad University
ORCID: 0009-0001-6710-2832
Observed ORCID: 0009-0001-6710-2832
OpenAlex ID: A5079051361
Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients
2023 · Karima Lafhal, Es-said Sabir, et al. · Molecular Genetics and Metabolism Reports · 10
Sphingolipidoses in Morocco: Chemical profiling for an affordable and rapid diagnosis strategy
2023 · M. Hammoud, A.M.S. Rodrigues, et al. · Prostaglandins & Other Lipid Mediators · 6
Metachromatic Leukodystrophy in Morocco: Identification of Causative Variants by Next-Generation Sequencing (NGS)
2024 · Miloud Hammoud, María Domínguez-Ruiz, et al. · Genes · 4
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Exploring inherited vitamin B responsive disorders in the Moroccan population: cutting-edge diagnosis via GC-MS profiling
2025 · Samira Najeh, Es-Said Sabir, et al. · Turkish Journal of Biochemistry · 2
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Novel HEXB variant and first evidence of urinary Gb4 isoforms in Sandhoff disease: Biochemical and bioinformatic characterization in two Moroccan families
2026 · Miloud Hammoud, Alice M.S. Rodrigues, et al. · Analytical Biochemistry · 1
Identification of a novel nonsense mutation in the AGL gene in glycogen storage disease type IIIa: first genetically confirmed case report from Morocco
2025 · Maroua Jakani, Imane Assiri, et al. · Molecular Biology Reports · 1
Sialic acid-Retaled disorders: Advances in pathophysiology, diagnostic challenges, and differentiating mimics
2025 · Imane Assiri, Naima Fdil · Clinica Chimica Acta · 1
From guidelines to real-world practice: clinical, biochemical, and genetic insights in a series of Moroccan patients with acid sphingomyelinase deficiency
2026 · Imane Assiri, Miloud Hammoud, et al. · Journal of Pediatric Endocrinology and Metabolism
Urinary sphingomyelin measurement: A simple tool for diagnosis and monitoring in Niemann-Pick disease type A
2026 · Imane Assiri, Samira Najeh, et al. · Molecular Genetics and Metabolism
Metabolomic profiling of rosa damascena mill. Hydroethanolic extracts reveals complex chelating signatures relevant to copper overload disorders
2026 · Abdelaati Berrachid, Jean-Pierre Mbakidi, et al. · Molecular Genetics and Metabolism
Hereditary tyrosinemia in Morocco: Clinical spectrum, diagnostic challenges, and genetic insights
2026 · Samira Najeh, Miloud Hammoud, et al. · Molecular Genetics and Metabolism
Zinc overload-induced copper deficiency as a treatable cause of peripheral neuropathy: Report of two cases
2026 · Sana E.L. Foutat, Karima Lafhal, et al. · Molecular Genetics and Metabolism
Detection of Gb3 and lactosylceramide in non-Fabry urine samples: Insights into the biochemical landscape of lysosomal disorders
2026 · Miloud Hammoud, Imane Assiri, et al. · Molecular Genetics and Metabolism
Rational diagnostic approach to Tay-Sachs disease highlighting urinary ganglioside excretion
2026 · Maroua Jakani, Mariam Lagrine, et al. · Molecular Genetics and Metabolism
Assessment of trace elements in the serum of epileptic patients with inherited metabolic diseases: Focus on zinc and copper
2025 · Sana El Foutat, Karima Lafhal, et al. · Molecular Genetics and Metabolism
First comprehensive identification of urinary sphingomyelin species in Niemann-Pick disease patients using UHPLC-MS/MS
2025 · Imane Assiri, Miloud Hammoud, et al. · Molecular Genetics and Metabolism
The bioactive potential of Rosa damascena mill: Preventive chelating effects and the role of ecosystem dynamics in inherited diseases
2025 · Abdelaati Berrachid, Karima Lafhal, et al. · Molecular Genetics and Metabolism
Assessment of carnitine deficiency in Moroccan patients: A high sensitivity and specificity enzymatic approach
2025 · Samira Najeh, Es-Said Sabir, et al. · Molecular Genetics and Metabolism
The evaluation of sulfatides in urine and dried blood spots as potential biomarkers for neurodegenerative diseases
2025 · Miloud Hammoud, Imane Assiri, et al. · Molecular Genetics and Metabolism
Altered ganglioside pattern in the infantile form of GM1 gangliosidosis identified using reversed-phase chromatography combined with thin-layer chromatography
2025 · Maroua Jakani, Sana El Foutat, et al. · Molecular Genetics and Metabolism
Molecular analysis of mucopolysaccharidosis type I in Morocco: Identification of novel mutation
2024 · Es-Said Sabir, Samira Najeh, et al. · Molecular Genetics and Metabolism
The utilization of a combination of TLC-UHPL/MS-MS and molecular networking in the assessment and prediction of Fabry and Sandhoff diseases
2024 · Miloud Hammoud, Imane Assiri, et al. · Molecular Genetics and Metabolism
A simple, non-invasive method for the diagnosis of glycogen storage disease type III in two patients with a similar facial appearance
2024 · Maroua Jakani, Miloud Hammoud, et al. · Molecular Genetics and Metabolism
The role of GC–MS in organic acidurias diagnosis in Moroccan population
2024 · Samira Najeh, Es-Said Sabir, et al. · Molecular Genetics and Metabolism
Clinical features of Wilson disease in Moroccan cohort
2024 · Karima Lafhal, Es-Said Sabir, et al. · Molecular Genetics and Metabolism
Works count: 34
Citation count: 25
H-index: 3
I10-index: 1
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