A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia

Autor Smaili, Imane, Hajjaj, Imane, Razine, Rachid, Tibar, Houyam, Salmi, Ayyoub, Bouslam, Naima, Moussa, Ahmed, Regragui, Wafa, Bouhouche, Ahmed
Vydáno v Case Rep Genet (2020)

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

Autor Ben El Haj, Rafiqua, Regragui, Wafaa, Tazi-Ahnini, Rachid, Skalli, Asmae, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Vydáno v Biomed Res Int (2016)

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

Autor Bouhouche, Ahmed, Tibar, Houyam, Kriouale, Yamna, Jiddane, Mohammed, Smaili, Imane, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, El Fahime, Elmostafa
Vydáno v Case Rep Genet (2018)

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

Autor Ben El Haj, Rafiqua, Salmi, Ayyoub, Regragui, Wafa, Moussa, Ahmed, Bouslam, Naima, Tibar, Houyam, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Vydáno v PLoS One (2017)

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

Autor Ouchkat, Fatima, Regragui, Wafaa, Smaili, Imane, Naciri Darai, Hajar, Bouslam, Naima, Rahmani, Mounia, Melhaoui, Adyl, Arkha, Yasser, El Fahime, Elmostafa, Bouhouche, Ahmed
Vydáno v BMC Med Genet (2020)

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

Autor 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
Vydáno 2012

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

Autor 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
Vydáno v Parkinsons Dis (2017)

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

Autor 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
Vydáno v Front Neurol (2017)

Clinical and genetic data of Huntington disease in Moroccan patients

Autor Bouhouche, Ahmed, Regragui, Wafaa, Lamghari, Hind, Khaldi, Khadija, Birouk, Nazha, Lytim, Safaa, Bellamine, Soufiane, Kriouile, Yamna, Bouslam, Naima, Haddou, El Hachmia Ait Ben, Faris, Mustapha Alaoui, Benomar, Ali, Yahyaoui, Mohamed
Vydáno v Afr Health Sci (2015)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Autor Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuck, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Bencheikh, Bouchra Ouled Amar
Vydáno v Am J Hum Genet (2016)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Autor Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Bencheikh, Bouchra Ouled Amar
Vydáno v Am J Hum Genet (2016)

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Autor Tesson, Christelle, Nawara, Magdalena, Salih, Mustafa A.M., Rossignol, Rodrigue, Zaki, Maha S., Al Balwi, Mohammed, Schule, Rebecca, Mignot, Cyril, Obre, Emilie, Bouhouche, Ahmed, Santorelli, Filippo M., Durand, Christelle M., Oteyza, Andrés Caballero, El-Hachimi, Khalid H., Al Drees, Abdulmajeed, Bouslam, Naima, Lamari, Foudil, Elmalik, Salah A., Kabiraj, Mohammad M., Seidahmed, Mohammed Z., Esteves, Typhaine, Gaussen, Marion, Monin, Marie-Lorraine, Gyapay, Gabor, Lechner, Doris, Gonzalez, Michael, Depienne, Christel, Mochel, Fanny, Lavie, Julie, Schols, Ludger, Lacombe, Didier, Yahyaoui, Mohamed, Al Abdulkareem, Ibrahim, Zuchner, Stephan, Yamashita, Atsushi, Benomar, Ali, Goizet, Cyril, Durr, Alexandra, Gleeson, Joseph G., Darios, Frederic, Brice, Alexis, Stevanin, Giovanni
Vydáno 2012

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

Autor Novarino, Gaia, Fenstermaker, Ali G., Zaki, Maha S., Hofree, Matan, Silhavy, Jennifer L., Heiberg, Andrew D., Abdellateef, Mostafa, Rosti, Basak, Scott, Eric, Mansour, Lobna, Masri, Amira, Kayserili, Hulya, Al-Aama, Jumana Y., Abdel-Salam, Ghada M. H., Karminejad, Ariana, Kara, Majdi, Kara, Bulent, Bozorgmehri, Bita, Ben-Omran, Tawfeg, Mojahedi, Faezeh, El Din Mahmoud, Iman Gamal, Bouslam, Naima, Bouhouche, Ahmed, Benomar, Ali, Hanein, Sylvain, Raymond, Laure, Forlani, Sylvie, Mascaro, Massimo, Selim, Laila, Shehata, Nabil, Al-Allawi, Nasir, Bindu, P.S., Azam, Matloob, Gunel, Murat, Caglayan, Ahmet, Bilguvar, Kaya, Tolun, Aslihan, Issa, Mahmoud Y., Schroth, Jana, Spencer, Emily G., Rosti, Rasim O., Akizu, Naiara, Vaux, Keith K., Johansen, Anide, Koh, Alice A., Megahed, Hisham, Durr, Alexandra, Brice, Alexis, Stevanin, Giovanni, Gabriel, Stacy B., Ideker, Trey, Gleeson, Joseph G.
Vydáno 2014