الرئيسية › دليل الباحثين › Miloud Hammoud
Miloud Hammoud
الانتماء : Cadi Ayyad University
- 36منشورات (انتماء مغربي)
- 42مجموع المنشورات
- 48الاستشهادات
- 4مؤشر h
الملف البحثي
لدى Miloud Hammoud 36 منشور(ات) مفهرسة (2020–2026). 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 «Ameliorative effect of Ononis natrix against chronic lead poisoning in mice: neurobehavioral, biochemical, and histological study» (2024)، وقد استُشهد به 10 مرة. 22 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل.
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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
- Heavy Metal Exposure and Toxicity
المنشورات (36)
- 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
- 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
- Ameliorative effect of Ononis natrix against chronic lead poisoning in mice: neurobehavioral, biochemical, and histological study
- Planar non-contact microwave sensor for the detection of aqueous organic and inorganic samples
- Metachromatic Leukodystrophy in Morocco: Identification of Causative Variants by Next-Generation Sequencing (NGS)
- 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
- Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients
- Non-Motor Symptoms in Parkinson's Disease
- 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
- Diagnosis of vitamin B deficiencies inducing inherited metabolic diseases (IMD) using GC-MS
- The case of glycosylation defects mimicking Wilson disease: A case report
- 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
- COVID-19
- 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
- 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
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
- 20266
- 20258
- 20248
- 20237
- 20223
- 20213
- 20201
التعاون العلمي
المؤسسات الشريكة : Centre Hospitalier Universitaire Mohammed VI · Université Sultan Moulay Slimane · Chouaib Doukkali University · Instituts Supérieurs des Professions Infirmières et Techniques de Santé · University of Hassan II Casablanca
المؤلفون المشاركون
- Naı̈ma Fdil
- Karima Lafhal
- Es‐Said Sabir
- 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).
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