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 no Biomed Res Int (2016)

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 em 2014

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 em 2012

Clinical and genetic data of Huntington disease in Moroccan patients

Por 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
Publicado no Afr Health Sci (2015)

Ataxia with Vitamin E Deficiency: Refinement of Genetic Localization and Analysis of Linkage Disequilibrium by Using New Markers in 14 Families

Por Doerflinger, Nathalie, Linder, Catherine, Ouahchi, Karim, Gyapay, Gabor, Weissenbach, Jean, Le Paslier, Denis, Rigault, Philippe, Belal, Samir, Hamida, Christiane Ben, Hentati, Faycal, Hamida, Mongi Ben, Pandolfo, Massimo, DiDonato, Stephano, Sokol, Ronald, Kayden, Herbert, Landrieu, Pierre, Durr, Alexandra, Brice, Alexis, Goutières, Françoise, Kohlschütter, Alfried, Sabouraud, Pascal, Benomar, Ali, Yahyaoui, Mohamed, Mandel, Jean-Louis, Koenig, Michel
Publicado em 1995

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Por 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
Publicado no Am J Hum Genet (2016)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Por 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
Publicado no Am J Hum Genet (2016)

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

Por 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
Publicado em 2012