Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report

por Ouchkat, Fatima, Regragui, Wafaa, Smaili, Imane, Naciri Darai, Hajar, Bouslam, Naima, Rahmani, Mounia, Melhaoui, Adyl, Arkha, Yasser, El Fahime, Elmostafa, Bouhouche, Ahmed
Publicado 2020

Bilateral brachial plexus injury following acute carbon monoxide poisoning

por Rahmani, Mounia, Belaidi, Halima, Benabdeljlil, Maria, Bouchhab, Wafa, El Jazouli, Nadia, El Brini, Asmae, Aidi, Saadia, Ouazzani, Reda M, El Alaoui Faris, Mustapha
Publicado 2013

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel

por Bouhouche, Ahmed, Tesson, Christelle, Regragui, Wafaa, Rahmani, Mounia, Drouet, Valérie, Tibar, Houyam, Souirti, Zouhayr, Ben El Haj, Rafiqua, Bouslam, Naima, Yahyaoui, Mohamed, Brice, Alexis, Benomar, Ali, Lesage, Suzanne
Publicado 2017

Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat

por Rahmani, Mounia, Benabdeljlil, Maria, Bellakhdar, Fouad, Faris, Mustapha El Alaoui, Jiddane, Mohamed, Bayad, Khalil El, Boutbib, Fatima, Razine, Rachid, Gana, Rachid, Hassani, Moulay R. El, Fatemi, Nizar El, Fikri, Meryem, Sanhaji, Siham, Tassine, Hennou, Balrhiti, Imane El Alaoui, Hadri, Souad El, Kettani, Najwa Ech-Cherif, Abbadi, Najia El, Amor, Mourad, Moussaoui, Abdelmjid, Semlali, Afifa, Aidi, Saadia, Benhaddou, El Hachmia Ait, Benomar, Ali, Bouhouche, Ahmed, Yahyaoui, Mohamed, Khamlichi, Abdeslam El, Ouahabi, Abdessamad El, Maaqili, Rachid El, Tibar, Houyam, Arkha, Yasser, Melhaoui, Adyl, Benazzouz, Abdelhamid, Regragui, Wafa
Publicado 2018