Naı̈ma Fdil

The emerging role of trace elements in epilepsy and metabolic disorders: a new frontier in neurotherapeutics

Sana El foutat, Abdelaati El Khiat, Naı̈ma Fdil

Maroc (code pays fourni par la source)

Synthesis, characterization, and antibacterial activity of novel hybrid purine-triazole Schiff base derivatives

Khadija Khaldoune, Meriem Rafya, Nouhaila Ait Lahcen, Ismail Hdoufane et autres

Maroc, lv (code pays fourni par la source)

Identifying barriers and policy priorities for rare disease research in underrepresented European countries

Baiba Lāce, Inna Inashkina, Dorica Dan, Ariane Weinman et autres

lv, fr, us, lt, ie (code pays fourni par la source)

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

Miloud Hammoud, Alice.M.S. Rodrigues, Imane Assiri, Samira Najeh et autres

Maroc, fr (code pays fourni par la source)

Schiff base cadmium complexes: Synthesis, crystal structure, theoretical studies and antibacterial activity

A. Hasnaoui, Khadija Khaldoune, Abd Elaziz Rahhou, Nouhaila Ait Lahcen et autres

Maroc, us, sa (code pays fourni par la source)

Prenatal alcohol exposure induces anxiety and depressive-like behaviors with deficits in growth and food intake in mice

Kamal Smimih, Bilal El-Mansoury, Mohamed Marghich, Chaima Azzouhri et autres

Maroc, sa, us (code pays fourni par la source)

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

Imane Assiri, Samira Najeh, Es‐Said Sabir, Maroua Jakani et autres

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

Abdelaati Berrachid, Jean‐Pierre Mbakidi, Karima Lafhal, Miloud Hammoud et autres

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

Samira Najeh, Miloud Hammoud, Es‐Said Sabir, Imane Assiri et autres

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

Sana El Foutat, Karima Lafhal, Abdelaati Berrachid, Es‐Said Sabir et autres

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

Miloud Hammoud, Imane Assiri, Samira Najeh, Maroua Jakani et autres

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

Maroua Jakani, Mariam Lagrine, Miloud Hammoud, Samira Najeh et autres