Polyradiculonévrite aiguë et Covid-19 : à propos de 3 observations

por Syrine, Lagha, Belarbi, Safae, Lahjomri, Ismail, Ouammou, Alas, Tibar, Houyam, Benomar, Ali, Hsaini, Yahya
Publicado 2022

A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis

por Aasfara, Jehanne, Regragui, Wafa, Ouardi, Loubna El, Haddou, El Hachmia Ait Ben, Benomar, Ali, Yahyaoui, Mohammed
Publicado 2019

A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism

por Ben El Haj, Rafiqua, Regragui, Wafaa, Tazi-Ahnini, Rachid, Skalli, Asmae, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Publicado 2016

Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing

por Bouhouche, Ahmed, Tibar, Houyam, Kriouale, Yamna, Jiddane, Mohammed, Smaili, Imane, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, El Fahime, Elmostafa
Publicado 2018

Evidence for prehistoric origins of the G2019S mutation in the North African Berber population

por Ben El Haj, Rafiqua, Salmi, Ayyoub, Regragui, Wafa, Moussa, Ahmed, Bouslam, Naima, Tibar, Houyam, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Publicado 2017

Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients

por Tibar, Houyam, El Bayad, Khalil, Bouhouche, Ahmed, Ait Ben Haddou, El Hachmia, Benomar, Ali, Yahyaoui, Mohamed, Benazzouz, Abdelhamid, Regragui, Wafa
Publicado 2018

Profile of idiopathic parkinson’s disease in Moroccan patients

por Regragui, Wafa, Lachhab, Lamiae, Razine, Rachid, Raissouni, Leila, Rasmouni, Khaoula, Imounan, Fatima, Benhaddou, El hachmia Ait, Abouqal, Redouane, Benomar, Ali, Yahyaoui, Mohamed
Publicado 2014

Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study

por Cheikh, Amine, Ajaja, Mohamed Rida, Rhazali, Hicham, Bouatia, Mustapha, Benomar, Ali, Slaoui, Anas, Cherrah, Yahia, Abouqal, Redouane, El Hassani, Amine, Cheikhaoui, Younes
Publicado 2019

An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3

por Bouhouche, Ahmed, Benomar, Ali, Errguig, Leila, Lachhab, Lamiae, Bouslam, Naima, Aasfara, Jehanne, Sefiani, Sanaa, Chabraoui, Layachi, El Fahime, Elmostafa, El Quessar, Abdeljalil, Jiddane, Mohamed, Yahyaoui, Mohamed
Publicado 2012

LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease

por Bouhouche, Ahmed, Tibar, Houyam, Ben El Haj, Rafiqua, El Bayad, Khalil, Razine, Rachid, Tazrout, Sanaa, Skalli, Asmae, Bouslam, Naima, Elouardi, Loubna, Benomar, Ali, Yahyaoui, Mohammed, Regragui, Wafa
Publicado 2017

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