Author

Miloud Hammoud

Observed institution: Cadi Ayyad University

ORCID: 0009-0004-9844-583X

Observed ORCID: 0009-0004-9844-583X

OpenAlex ID: A5004901592

Ameliorative effect of Ononis natrix against chronic lead poisoning in mice: neurobehavioral, biochemical, and histological study

2024 · Asmaa Haj-Khlifa, Faissal Aziz, et al. · Biological Trace Element Research · 10

Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients

2023 · Karima Lafhal, Es-said Sabir, et al. · Molecular Genetics and Metabolism Reports · 10

Non-Motor Symptoms in Parkinson's Disease

2023 · Bilal El-Mansoury, Abdelali Ben Maloui, et al. · Advances in medical diagnosis, treatment, and care (AMDTC) book series · 8

Planar non-contact microwave sensor for the detection of aqueous organic and inorganic samples

2024 · Abdessalam El Yassini, Miloud Hammoud, et al. · Sensors and Actuators A Physical · 5

Metachromatic Leukodystrophy in Morocco: Identification of Causative Variants by Next-Generation Sequencing (NGS)

2024 · Miloud Hammoud, María Domínguez-Ruiz, et al. · Genes · 4

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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

2022 · Sabir Es-said, Karima Lafhal, et al. · Pharmaceutical Biology · 4

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Exploring inherited vitamin B responsive disorders in the Moroccan population: cutting-edge diagnosis via GC-MS profiling

2025 · Samira Najeh, Es-Said Sabir, et al. · Turkish Journal of Biochemistry · 2

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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

2020 · Karima Lafhal, Es-said Sabir, et al. · Carbohydrate Research · 2

Novel HEXB variant and first evidence of urinary Gb4 isoforms in Sandhoff disease: Biochemical and bioinformatic characterization in two Moroccan families

2026 · Miloud Hammoud, Alice M.S. Rodrigues, et al. · Analytical Biochemistry · 1

Identification of a novel nonsense mutation in the AGL gene in glycogen storage disease type IIIa: first genetically confirmed case report from Morocco

2025 · Maroua Jakani, Imane Assiri, et al. · Molecular Biology Reports · 1

Protein Diet and Management of Hepatic Encephalopathy: An Overview of the Last Decade Controversy

2022 · Abdelmohcine Aimrane, Mehdi Ait-Laaradia, et al. · Springer eBooks · 1

COVID-19

2021 · Ahmed Draoui, Hicham Chatoui, et al. · Advances in medical diagnosis, treatment, and care (AMDTC) book series · 1

Rosa damascena Mill attenuated the liver and kidneys injuries in copper-overloaded mice

2021 · Karima Lafhal, Es-said Sabir, et al. · Molecular Genetics and Metabolism · 1

From guidelines to real-world practice: clinical, biochemical, and genetic insights in a series of Moroccan patients with acid sphingomyelinase deficiency

2026 · Imane Assiri, Miloud Hammoud, et al. · Journal of Pediatric Endocrinology and Metabolism

Urinary sphingomyelin measurement: A simple tool for diagnosis and monitoring in Niemann-Pick disease type A

2026 · Imane Assiri, Samira Najeh, et al. · Molecular Genetics and Metabolism

Metabolomic profiling of rosa damascena mill. Hydroethanolic extracts reveals complex chelating signatures relevant to copper overload disorders

2026 · Abdelaati Berrachid, Jean-Pierre Mbakidi, et al. · Molecular Genetics and Metabolism

Hereditary tyrosinemia in Morocco: Clinical spectrum, diagnostic challenges, and genetic insights

2026 · Samira Najeh, Miloud Hammoud, et al. · Molecular Genetics and Metabolism

Zinc overload-induced copper deficiency as a treatable cause of peripheral neuropathy: Report of two cases

2026 · Sana E.L. Foutat, Karima Lafhal, et al. · Molecular Genetics and Metabolism

Detection of Gb3 and lactosylceramide in non-Fabry urine samples: Insights into the biochemical landscape of lysosomal disorders

2026 · Miloud Hammoud, Imane Assiri, et al. · Molecular Genetics and Metabolism

Rational diagnostic approach to Tay-Sachs disease highlighting urinary ganglioside excretion

2026 · Maroua Jakani, Mariam Lagrine, et al. · Molecular Genetics and Metabolism

Assessment of trace elements in the serum of epileptic patients with inherited metabolic diseases: Focus on zinc and copper

2025 · Sana El Foutat, Karima Lafhal, et al. · Molecular Genetics and Metabolism

First comprehensive identification of urinary sphingomyelin species in Niemann-Pick disease patients using UHPLC-MS/MS

2025 · Imane Assiri, Miloud Hammoud, et al. · Molecular Genetics and Metabolism

The bioactive potential of Rosa damascena mill: Preventive chelating effects and the role of ecosystem dynamics in inherited diseases

2025 · Abdelaati Berrachid, Karima Lafhal, et al. · Molecular Genetics and Metabolism

Assessment of carnitine deficiency in Moroccan patients: A high sensitivity and specificity enzymatic approach

2025 · Samira Najeh, Es-Said Sabir, et al. · Molecular Genetics and Metabolism

The evaluation of sulfatides in urine and dried blood spots as potential biomarkers for neurodegenerative diseases

2025 · Miloud Hammoud, Imane Assiri, et al. · Molecular Genetics and Metabolism

Works count: 42

Citation count: 50

H-index: 4

I10-index: 2