الرئيسية › دليل الباحثين › Naı̈ma Fdil
Naı̈ma Fdil
الانتماء : Cadi Ayyad University
- 83منشورات (انتماء مغربي)
- 93مجموع المنشورات
- 561الاستشهادات
- 11مؤشر h
الملف البحثي
لدى Naı̈ma Fdil 83 منشور(ات) مفهرسة (1996–2026). تُنشر أعماله أساسًا في «Molecular Genetics and Metabolism»، «The American Journal of Gastroenterology» و«Advances in medical diagnosis, treatment, and care (AMDTC) book series». أكثر مقالاته استشهادًا هو «Antibacterial activity of Quercus ilex bark's extracts» (2007)، وقد استُشهد به 151 مرة. 36 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Metabolism and Genetic Disorders
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Trace Elements in Health
- Genomics and Rare Diseases
المنشورات (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
مجلات النشر
- 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
المنشورات حسب السنة
- 202610
- 202514
- 202412
- 202316
- 20228
- 20215
- 20205
- 20196
- 20171
- 20142
التعاون العلمي
المؤسسات الشريكة : Centre Hospitalier Universitaire Mohammed VI · Chouaib Doukkali University · Université Sultan Moulay Slimane · Instituts Supérieurs des Professions Infirmières et Techniques de Santé · Abdelmalek Essaâdi University
بلدان المؤلفين المشاركين : فرنسا
المؤلفون المشاركون
- 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
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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