Sökresultat - Bouslam, Naima

A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia av Smaili, Imane, Hajjaj, Imane, Razine, Rachid, Tibar, Houyam, Salmi, Ayyoub, Bouslam, Naima, Moussa, Ahmed, Regragui, Wafa, Bouhouche, Ahmed

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A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism av Ben El Haj, Rafiqua, Regragui, Wafaa, Tazi-Ahnini, Rachid, Skalli, Asmae, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed

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Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing av Bouhouche, Ahmed, Tibar, Houyam, Kriouale, Yamna, Jiddane, Mohammed, Smaili, Imane, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, El Fahime, Elmostafa

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Evidence for prehistoric origins of the G2019S mutation in the North African Berber population av Ben El Haj, Rafiqua, Salmi, Ayyoub, Regragui, Wafa, Moussa, Ahmed, Bouslam, Naima, Tibar, Houyam, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed

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Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report av Ouchkat, Fatima, Regragui, Wafaa, Smaili, Imane, Naciri Darai, Hajar, Bouslam, Naima, Rahmani, Mounia, Melhaoui, Adyl, Arkha, Yasser, El Fahime, Elmostafa, Bouhouche, Ahmed

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

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

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

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Clinical and genetic data of Huntington disease in Moroccan patients av 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

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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia av 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

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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia av 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

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

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Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders av 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.

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