الرئيسية › دليل الباحثين › Karima Lafhal
Karima Lafhal
الانتماء : Cadi Ayyad University · Instituts Supérieurs des Professions Infirmières et Techniques de Santé
- 43منشورات (انتماء مغربي)
- 48مجموع المنشورات
- 111الاستشهادات
- 5مؤشر h
الملف البحثي
لدى Karima Lafhal 43 منشور(ات) مفهرسة (2019–2026). تُنشر أعماله أساسًا في «Molecular Genetics and Metabolism»، «Advances in medical diagnosis, treatment, and care (AMDTC) book series» و«Analytical Biochemistry». أكثر مقالاته استشهادًا هو «Sub-acute toxicity of graphene oxide (GO) nanoparticles in male mice after intraperitoneal injection: Behavioral study and histopathological» (2022)، وقد استُشهد به 38 مرة. 22 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا.
هل هذا أنت؟ عرّف بأبحاثك
أنشئ ملفك على DzCademia مجانًا وأضف مقالاتك: ستظهر بسهولة أكبر على Google وفي مساعدي الذكاء الاصطناعي مثل ChatGPT، فيقرؤها ويستشهد بها عدد أكبر من الناس.
إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Metabolism and Genetic Disorders
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Trace Elements in Health
- Neurological diseases and metabolism
المنشورات (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
مجلات النشر
- 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
المنشورات حسب السنة
- 20265
- 202510
- 20247
- 20238
- 20225
- 20214
- 20202
- 20192
التعاون العلمي
المؤسسات الشريكة : Centre Hospitalier Universitaire Mohammed VI · Chouaib Doukkali University · Université Sultan Moulay Slimane · Université Ibn Zohr · Mohammed V University
بلدان المؤلفين المشاركين : فرنسا
المؤلفون المشاركون
- 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
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
لماذا تختارون Dzcademia؟
ملفات أكاديمية ومقالات ومداخلات علمية: امنحوا أبحاثكم حضوراً عاماً منظماً. تساعد البيانات الوصفية المدمجة محركات البحث ومساعدات الذكاء الاصطناعي على التعرف على أعمالكم وفهم مراجعها.
علّق عبر Google
سجّل الدخول عبر Google للتعليق مباشرة على هذه الصفحة.