Accueil › Annuaire des chercheurs › Karima Lafhal
Karima Lafhal
Affiliation : Cadi Ayyad University · Instituts Supérieurs des Professions Infirmières et Techniques de Santé
- 43Publications (affiliation marocaine)
- 48Publications au total
- 111Citations
- 5Indice h
Profil de recherche
Karima Lafhal compte 43 publications référencées (2019–2026). Ses travaux paraissent principalement dans « Molecular Genetics and Metabolism », « Advances in medical diagnosis, treatment, and care (AMDTC) book series » et « Analytical Biochemistry ». Son article le plus cité, « Sub-acute toxicity of graphene oxide (GO) nanoparticles in male mice after intraperitoneal injection: Behavioral study and histopathological » (2022), a été cité 38 fois. 22 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
- Neurological diseases and metabolism
Publications (43)
- 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
- Detection of Gb3 and lactosylceramide in non-Fabry urine samples: Insights into the biochemical landscape of lysosomal disorders
- 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
- 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
- Exploring the Nexus of Environmental Health and Nursing
- Therapeutic approaches using natural substances on the thioacetamide-induced animal model of acute liver failure: UHPLC analysis, biochemical and histopathological studies
- Wilson Disease: Diagnostic Challenges and Differential Diagnoses
- 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
- Exploring anticancer activity, acute toxicity, and molecular docking of synthesized schiff bases and schiff base-palladium complex
- Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients
- Sphingolipidoses in Morocco: Chemical profiling for an affordable and rapid diagnosis strategy
- Isolated lactosylceramide storage: Is it the consequence of a specific protein deficiency?
- 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
- 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
- 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
- Protein Diet and Management of Hepatic Encephalopathy: An Overview of the Last Decade Controversy
- 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
- COVID-19
- Insights Into the COVID-19 Infection Related to Inherited Metabolic Diseases
- 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
- 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
- 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
Revues de publication
- Molecular Genetics and Metabolism × 23
- Advances in medical diagnosis, treatment, and care (AMDTC) book series × 2
- Analytical Biochemistry × 1
- Journal of Pediatric Endocrinology and Metabolism × 1
- Turkish Journal of Biochemistry × 1
- Molecular Biology Reports × 1
Publications par année
- 20265
- 202510
- 20247
- 20238
- 20225
- 20214
- 20202
- 20192
Collaborations
Établissements partenaires : Centre Hospitalier Universitaire Mohammed VI · Chouaib Doukkali University · Université Sultan Moulay Slimane · Université Ibn Zohr · Mohammed V University
Pays des co-auteurs : France
Co-auteurs
- Naı̈ma Fdil
- Es‐Said Sabir
- Miloud Hammoud
- Imane Assiri
- Samira Najeh
- Maroua Jakani
- Abdelaati Berrachid
- Sana El Foutat
- Aïcha Bourrahouat
- My Ahmed Elamiri
- Mohammed Bouskraoui
- Lhoucine Gebrati
Données bibliographiques issues d’OpenAlex (base ouverte).
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