| FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies M Jalte, M Abbassi, H El Mouhi, HD Belghiti, M Ahakoud, H Bekkari Cureus 15 (9), 2023 | 13 | 2023 |
| A case of severe teratozoospermia and infertility due to homozygous mutation c. 144delC in the AURKC gene M Abbassi, H Sayel, H El Mouhi, M Jelte, M Ahakoud Cureus 15 (8), 2023 | 3 | 2023 |
| Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report H El Mouhi, N Amllal, M Abbassi, A Nedbour, M Jalte, J Lyahyai, ... Molecular Biology Reports 51 (1), 233, 2024 | 1 | 2024 |
| Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a … H El Mouhi, M Abbassi, H Sayel, S Trhanint, A Natiq, B El Hejjioui, M Jalte, ... Cureus 15 (10), 2023 | 1 | 2023 |
| Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation M Abbassi, A Bourmtane, H Sayel, H El Mouhi, M Jalte, YA Elasri, ... Molecular Biology Reports 50 (11), 9121-9128, 2023 | | 2023 |
| Identification of Novel and De Novo Mutation in the SCN1A Gene By Exome Sequencing Confirms Dravet Syndrome in Moroccan Child: A Case Report H EL MOUHI, N AMLLAL, M ABBASSI, A NEDBOUR, M JALTE, ... | | 2023 |
| A Mini Review of Doose Syndrome: Clinical Manifestations, Diagnosis, and Treatment M AHAKOUD, H EL MOUHI, HD BELGHITI, L BOUGUENOUCH, ... Moroccan Journal of Public Heath 5 (1), 2023 | | 2023 |
| Clinical Evidence of Circulating Tumor DNA Application in Aggressive Breast Cancer. Diagnostics 2023, 13, 470 B El Hejjioui, L Bouguenouch, MA Melhouf, H El Mouhi, S Bennis | | 2023 |
| SARS-CoV-2/HBV co-infection: case report H EL MOUHI, L BOUGUENOUCH, A NATIQ, B EL HEJJIOUI, H OUBIHI, ... Moroccan Journal of Public Heath 4 (1), 2022 | | 2022 |
