Accueil › Annuaire des chercheurs › Naı̈ma Fdil
Naı̈ma Fdil
Affiliation : Cadi Ayyad University
- 83Publications (affiliation marocaine)
- 93Publications au total
- 561Citations
- 11Indice h
Profil de recherche
Naı̈ma Fdil compte 83 publications référencées (1996–2026). Ses travaux paraissent principalement dans « Molecular Genetics and Metabolism », « The American Journal of Gastroenterology » et « Advances in medical diagnosis, treatment, and care (AMDTC) book series ». Son article le plus cité, « Antibacterial activity of Quercus ilex bark's extracts » (2007), a été cité 151 fois. 36 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Metabolism and Genetic Disorders
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Trace Elements in Health
- Genomics and Rare Diseases
Publications (83)
- Schiff base cadmium complexes: Synthesis, crystal structure, theoretical studies and antibacterial activity
- Novel HEXB variant and first evidence of urinary Gb4 isoforms in Sandhoff disease: Biochemical and bioinformatic characterization in two Moroccan families
- Urinary sphingomyelin measurement: A simple tool for diagnosis and monitoring in Niemann-Pick disease type A
- Metabolomic profiling of rosa damascena mill. Hydroethanolic extracts reveals complex chelating signatures relevant to copper overload disorders
- Hereditary tyrosinemia in Morocco: Clinical spectrum, diagnostic challenges, and genetic insights
- Detection of Gb3 and lactosylceramide in non-Fabry urine samples: Insights into the biochemical landscape of lysosomal disorders
- Prenatal alcohol exposure induces anxiety and depressive-like behaviors with deficits in growth and food intake in mice
- Synthesis, characterization, and antibacterial activity of novel hybrid purine-triazole Schiff base derivatives
- The emerging role of trace elements in epilepsy and metabolic disorders: a new frontier in neurotherapeutics
- From guidelines to real-world practice: clinical, biochemical, and genetic insights in a series of Moroccan patients with acid sphingomyelinase deficiency
- Exploring inherited vitamin B responsive disorders in the Moroccan population: cutting-edge diagnosis via GC-MS profiling
- Study on the biosynthesis and antibacterial effect of Zinc Oxide Nanoparticles using aloe vera latex extract
- Novel Schiff Base Cadmium Complexes: Synthesis, Crystal Structure and Antibacterial Activity
- Sialic acid-Retaled disorders: Advances in pathophysiology, diagnostic challenges, and differentiating mimics
- X-Linked Adrenoleukodystrophy in a Moroccan Patient: Genetic Diagnosis Leads to Presymptomatic Testing and Family Counseling
- Identification of a novel nonsense mutation in the AGL gene in glycogen storage disease type IIIa: first genetically confirmed case report from Morocco
- Assessment of trace elements in the serum of epileptic patients with inherited metabolic diseases: Focus on zinc and copper
- First comprehensive identification of urinary sphingomyelin species in Niemann-Pick disease patients using UHPLC-MS/MS
- The bioactive potential of Rosa damascena mill: Preventive chelating effects and the role of ecosystem dynamics in inherited diseases
- Assessment of carnitine deficiency in Moroccan patients: A high sensitivity and specificity enzymatic approach
- The evaluation of sulfatides in urine and dried blood spots as potential biomarkers for neurodegenerative diseases
- Altered ganglioside pattern in the infantile form of GM1 gangliosidosis identified using reversed-phase chromatography combined with thin-layer chromatography
- Therapeutic approaches using natural substances on the thioacetamide-induced animal model of acute liver failure: UHPLC analysis, biochemical and histopathological studies
- The involvement of underrepresented countries in the European rare diseases research alliance: Morocco’s assets
- Exploring Aloe vera: A comprehensive review on extraction, chemical composition, biological effects, and its utilization in the synthesis of metallic nanoparticles
- New Schiff bases and their vanadium complexes: Synthesis, characterization, and biological assessment for antibacterial and antiviral action
- Ameliorative effect of Ononis natrix against chronic lead poisoning in mice: neurobehavioral, biochemical, and histological study
- Wilson Disease: Diagnostic Challenges and Differential Diagnoses
- Metachromatic Leukodystrophy in Morocco: Identification of Causative Variants by Next-Generation Sequencing (NGS)
- Graphene Oxide (GO) Sub Chronic Toxicity in Liver, Kidney and Spleen: Macroscopic Observation and Histo-biochemical Examination
- Molecular analysis of mucopolysaccharidosis type I in Morocco: Identification of novel mutation
- The utilization of a combination of TLC-UHPL/MS-MS and molecular networking in the assessment and prediction of Fabry and Sandhoff diseases
- A simple, non-invasive method for the diagnosis of glycogen storage disease type III in two patients with a similar facial appearance
- The role of GC–MS in organic acidurias diagnosis in Moroccan population
- Clinical features of Wilson disease in Moroccan cohort
- Nutritional Recommendations for TBI Management
- Exploring anticancer activity, acute toxicity, and molecular docking of synthesized schiff bases and schiff base-palladium complex
- Hyperammonemia induces gut microbiota dysbiosis and motor coordination disturbances in mice: new insight into gut‑brain axis involvement in hepatic encephalopathy
- Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients
- Sphingolipidoses in Morocco: Chemical profiling for an affordable and rapid diagnosis strategy
- P14 Altered Locomotor Behavior Associated With Purkinje Cells and Astrocytes Dysfunctions in Rat With Acute Hepatic Encephalopathy Involving the Oxidative Stress and Neuroinflammation
- Urinary Glycosaminoglycans: Characterization and Quantification
- Isolated lactosylceramide storage: Is it the consequence of a specific protein deficiency?
- Next-generation sequencing and high-throughput enzymolome-based panel screening of suspected lysosomal disease cases identifies multiple disease-causing variants in two genes underlying different lysosomal diseases: A source of clinical and metabolic variability?
- Timely diagnosis of Niemann Pick disease using thin layer chromatography with identification of SMPD1 mutations causing NPD type A/B among Moroccan population
- The role of combination between TLC and UHPL/MS-MS in the diagnosis and prognosis of metachromatic leukodystrophy
- Diagnosis of vitamin B deficiencies inducing inherited metabolic diseases (IMD) using GC-MS
- Identification of the first genetic variants underlying metachromatic leukodystrophy in the Moroccan population by biochemical analyses and NGS-based genetic screening
- The case of glycosylation defects mimicking Wilson disease: A case report
- P1 Gut Dysbiosis in Hyperammonemic Mice and Motor Incoordination: A New Discernment of the Gut-Brain Axis in Hepatic Encephalopathy
- Therapeutic Strategies for Lysosomal Storage Diseases by Targeting Glial Cells
- Direct contribution of Purkinje neurons death and morpho-functional astroglial changes involving oxidative stress and neuroinflammation in the pathogenesis of hepatic encephalopathy
- Insight into COVID-19's epidemiology, pathology, and treatment
- Sub-acute toxicity of graphene oxide (GO) nanoparticles in male mice after intraperitoneal injection: Behavioral study and histopathological evaluation
- Flaxseed extract reduces tissue accumulation and enhances urinary excretion of chondroitin sulphate in the rat: a possible new path in substrate reduction therapy for mucopolysaccharidosis
- Genetic screening of lysosomal disorders: An account of five years' experience with NGS-based resequencing panels
- Protein Diet and Management of Hepatic Encephalopathy: An Overview of the Last Decade Controversy
- NGS-based panel screening of suspected lysosomal disease cases identifies novel pathogenic variants underlying acid sphingomyelinase deficiency (ASMD), Krabbe disease, and lymphatic dysplasia with non-immune hydrops fetalis
- Determination of urinary mannose by gas liquid chromatography mass spectrometry using a dried urine spot
- A novel nonsense MPS VI mutation in a south Moroccan patient
- Time dependent alteration of locomotor behavior in rat with acute liver failure induced cerebellar neuroinflammation and neuro-astroglial damage
- Insights Into the COVID-19 Infection Related to Inherited Metabolic Diseases
- SARS-Cov-2 and Associated Heart Failure
- An affordable combined method to achieve a confirming diagnosis of metachromatic leukodystrophy
- Chelating effect of flax seed extract in rats overloaded with chondroitin sulfate: A new path in substrate reduction therapy for mucoplysccharidosis
- Usefulness of urinary glycosaminoglycans assay for a mucopolysaccharidosis‐specific screening
- Implementation of an Affordable Method for MPS Diagnosis from Urine Screening to Enzymatic Confirmation: Results of a Pilot Study in Morocco
- Synthesis and Characterization of New Chalcone Derivatives of Aryl-Himachalene
- The Lysosomal Storage Diseases: A Promising Axis for COVID-19 Future Therapies
- 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 diseases
- Infantile GM1-Gangliosidosis Revealed by Slate-Grey Mongolian Spots
- Le déficit en carnitine palmitoyl transférase : à propos de deux cas
- Development of a technical colorimetric for the determination of galactosis in blood
- Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene (ARSB) in Moroccan patient
- NGS-based, 107-gene resequencing panel as first-line screening test for lysosomal diseases
- First case of hereditary xanthinuria in a Moroccan family
- Lipoprotein Lipase (LPL) Gene Mutation: A First Report in Children
- Les mycoses du pied chez le diabétique : étude pilote réalisée au CHU Mohamed VI de Marrakech
- Blastomycose cutanée isolée révélant un carcinome spinocellulaire
- Antibacterial activity of Quercus ilex bark's extracts
- Isolation and antimicrobial activity of two phenolic compounds from Pulicaria odora L.
- Epoxydation aerobique des terpenes naturels: etude de l'activité catalytique des nouveaux complexes Ru-1,2,4-triazepines
- Terpenic olefin epoxidation using metals acetylacetonates as catalysts
Revues de publication
- Molecular Genetics and Metabolism × 30
- The American Journal of Gastroenterology × 2
- Advances in medical diagnosis, treatment, and care (AMDTC) book series × 2
- Journal de Mycologie Médicale × 2
- Journal of Ethnopharmacology × 2
- Journal of Molecular Structure × 1
Publications par année
- 202610
- 202514
- 202412
- 202316
- 20228
- 20215
- 20205
- 20196
- 20171
- 20142
Collaborations
Établissements partenaires : Centre Hospitalier Universitaire Mohammed VI · Chouaib Doukkali University · Université Sultan Moulay Slimane · Instituts Supérieurs des Professions Infirmières et Techniques de Santé · Abdelmalek Essaâdi University
Pays des co-auteurs : France
Co-auteurs
- Karima Lafhal
- Es‐Said Sabir
- Miloud Hammoud
- Imane Assiri
- Samira Najeh
- Maroua Jakani
- Abdelaati Berrachid
- Sana El Foutat
- Aïcha Bourrahouat
- Mohammed Bouskraoui
- My Ahmed Elamiri
- Aïcha Ezoubeiri
Données bibliographiques issues d’OpenAlex (base ouverte).
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