| Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder K Rochdi, M Cerino, N Da Silva, V Delague, A Bouzidi, H Nahili, G Zouiri, ... Clinica Chimica Acta 524, 51-58, 2022 | 3 | 2022 |
| A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration S Efthymiou, Y Kriouile, V Salpietro, R Hajar, Z Ghizlane, K Mankad, ... Journal of the Neurological Sciences 410, 2020 | 3 | 2020 |
| Syndrome de Sturge-Weber-Krabbe: à propos de 6 cas G Zouiri, A Ahmina, Y Kriouile Research 1, 894, 2014 | 3 | 2014 |
| Le syndrome de Lennox Gastaut: à propos de 27 cas G Zouiri, Y Kriouile African & Middle East Epilepsy Journal 1 (6), 2012 | 3 | 2012 |
| Pathologic Confirmation of Lafora Disease H Rhouda, A Malihy, G Zouiri, Y Kriouile Pediatric Neurology 108, 128, 2020 | 1 | 2020 |
| Syndrome de Guillain-Barré à reflexes conservés G Zouiri, R Abilkassem, A Zerhouni, N Dini, A Agadr Archives de Pédiatrie 23 (5), 501-503, 2016 | 1 | 2016 |
| Guillain-Barré syndrome with preserved reflexes G Zouiri, R Abilkassem, A Zerhouni, N Dini, A Agadr Archives de Pediatrie: Organe Officiel de la Societe Francaise de Pediatrie …, 2016 | 1 | 2016 |
| c. 754T> A homozygous mutation described for the first time in three Moroccan patients with Gaucher disease G Zouiri, H Rhouda, Y Kriouile Archives de Pédiatrie, 2024 | | 2024 |
| Pediatrics 2 experience, Neuropediatrics and neurometabolic diseases unit on phenylcetonuria: About 36 patients FE IRINEU, H LACHRAF, H RHOUDA, G ZOUIRI, S MOUSSAOUI, ... World Journal of Advanced Research and Reviews 22 (1), 201-205, 2024 | | 2024 |
| Gaucher disease: About an observation FE IRINEU, G ZOUIRI, H RHOUDA, H LACHRAF, S MOUSSAOUI, H LAJI, ... World Journal of Advanced Research and Reviews 22 (1), 196-200, 2024 | | 2024 |
| Pelizaeus disease Merzbacher like: About an observation FE IRINEU, H LACHRAF, H RHOUDA, G ZOUIRI, S MOUSSAOUI, H LAJI, ... World Journal of Advanced Research and Reviews 22 (1), 206-209, 2024 | | 2024 |
| Novel variant in Moroccan patient with hereditary spastic paraplegia type 35 N Sifeddine, G Amalou, A Bouzidi, M Charif, H Nahili, G Zouiri, R Hajar, ... Human Gene 38, 201230, 2023 | | 2023 |
| GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families. N Sifeddine, G Amalou, M Charif, H Nahili, A Bouzidi, R Salaheddine, ... Muscles, Ligaments & Tendons Journal (MLTJ) 13 (4), 2023 | | 2023 |
| Anti-NMDA Receptor Encephalitis in Children M Kabbaj, G Zouiri, H GHOUDA, Y Kriouile Sch J Med Case Rep 10, 1020-1022, 2022 | | 2022 |
| A misleading presentation of juvenile Tay Sachs disease G Zouiri, H Rhouda, Y Kriouile Revue neurologique 176 (3), 213-214, 2020 | | 2020 |
| Angiome plan de la face: À propos de deux cas dont l'un révélant un syndrome de Sturge Weber et Krabb. BMA Tiemtoré-Kambou, NA Ouédraogo, F Traoré, PA Ouédraogo, ... Our Dermatology Online/Nasza Dermatologia Online 8 (1), 2017 | | 2017 |
| International Journal of Current Advanced Research I Elouardighi, N Mekaoui, G Zouiri, L Karboubi, B Benjelloun medicine 3, 4, 2017 | | 2017 |
| LES MALADIES MITOCHONDRIALES: PREVALENCE, ASPECTS CLINIQUES, BIOLOGIQUES ET GENETIQUES Z GHIZLANE | | 2016 |
| Feverish Agitation Unveiling a Poly Poisoning in Young Children G Zouiri, MA Radouani, N Badrane, A Assermouh, F Benbrahim J Pediatr Neonatal Care 2 (1), 00052, 2015 | | 2015 |
| CMMR-D syndrome: à propos d’une observation G ZOUIRI, PA KILI | | 2014 |
