Get started
Author

Sana El Foutat

Observed names: Sana E.L. Foutat, Sana E.L. foutat, Sana EL Foutat, Sana El foutat, Sana Elfoutat
Observed institution: Cadi Ayyad University
OpenAlex ID: A5115396809
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
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
The emerging role of trace elements in epilepsy and metabolic disorders: a new frontier in neurotherapeutics
2026 · Sana EL Foutat, Abdelaati EL Khiat, et al. · BioMetals
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
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
Nutritional Recommendations for TBI Management
2024 · Sana El Foutat, Abdelaati El Khiat, et al. · Nutritional neurosciences
Magnesium and Traumatic Brain Injury
2024 · Abdelaati El Khiat, Sana El Foutat, et al. · Nutritional neurosciences
Works count: 17
Citation count: 2
H-index: 1
I10-index:
Year
Topic
Type