Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients
Tibar, Houyam, El Bayad, Khalil, Bouhouche, Ahmed, Ait Ben Haddou, El Hachmia, Benomar, Ali, Yahyaoui, Mohamed, Benazzouz, Abdelhamid, Regragui, Wafa
Published in Frontiers in neurology (04.04.2018)
Published in Frontiers in neurology (04.04.2018)
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Headache and Status Epilepticus Reveal Paget's Disease of the Bone
Ouhabi, Dahab, Tibar, Houyam, Benomar, Ali, Jiddane, Mohamed, Regragui, Wafa
Published in Curēus (Palo Alto, CA) (19.05.2024)
Published in Curēus (Palo Alto, CA) (19.05.2024)
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Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
Roux, Thomas, Barbier, Mathieu, Papin, Mélanie, Davoine, Claire-Sophie, Sayah, Sabrina, Coarelli, Giulia, Charles, Perrine, Marelli, Cecilia, Parodi, Livia, Tranchant, Christine, Goizet, Cyril, Klebe, Stephan, Lohmann, Ebba, Van Maldergem, Lionel, van Broeckhoven, Christine, Coutelier, Marie, Tesson, Christelle, Stevanin, Giovanni, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra
Published in Genetics in medicine (01.11.2020)
Published in Genetics in medicine (01.11.2020)
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Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease
Smaili, Imane, Tesson, Christelle, Regragui, Wafa, Bertrand, Hélène, Rahmani, Mounia, Bouslam, Naima, Benomar, Ali, Brice, Alexis, Lesage, Suzanne, Bouhouche, Ahmed
Published in Journal of molecular neuroscience (2021)
Published in Journal of molecular neuroscience (2021)
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Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome
Hanein, Sylvain, Martin, Elodie, Boukhris, Amir, Byrne, Paula, Goizet, Cyril, Hamri, Abdelmadjid, Benomar, Ali, Lossos, Alexander, Denora, Paola, Fernandez, José, Elleuch, Nizar, Forlani, Sylvie, Durr, Alexandra, Feki, Imed, Hutchinson, Michael, Santorelli, Filippo M., Mhiri, Chokri, Brice, Alexis, Stevanin, Giovanni
Published in American journal of human genetics (01.04.2008)
Published in American journal of human genetics (01.04.2008)
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Evidence for prehistoric origins of the G2019S mutation in the North African Berber population
Ben El Haj, Rafiqua, Salmi, Ayyoub, Regragui, Wafa, Moussa, Ahmed, Bouslam, Naima, Tibar, Houyam, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Published in PloS one (19.07.2017)
Published in PloS one (19.07.2017)
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LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease
Benomar, Ali, Yahyaoui, Mohamed, Regragui, Wafaa, Bouslam, Naima, Skalli, Asmae, Tazrout, Sanaa, Razine, Rachid, El Bayad, Khalil, Ben El Haj, Rafiqua, Tibar, Houyam, Bouhouche, Ahmed, Elouardi, Loubna
Published in Parkinson's disease (01.01.2017)
Published in Parkinson's disease (01.01.2017)
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Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
Roux, Thomas, Barbier, Mathieu, Papin, Mélanie, Davoine, Claire-Sophie, Sayah, Sabrina, Coarelli, Giulia, Charles, Perrine, Marelli, Cecilia, Parodi, Livia, Tranchant, Christine, Goizet, Cyril, Klebe, Stephan, Lohmann, Ebba, Van Maldergem, Lionel, van Broeckhoven, Christine, Coutelier, Marie, Tesson, Christelle, Stevanin, Giovanni, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Durr, Alexandra, Stevanin, Giovanni, Brice, Alexis, Darios, Frédéric, Forlani, Sylvie, Site, Pitié-Salpêtrière, Banneau, Guillaume, Cazeneuve, Cécile, Charles, Perrine, Duyckaerts, Charles, Fontaine, Bertrand, Azulay, Jean-Philippe, Boesfplug-Tanguy, Odile, Goizet, Cyril, Hannequin, Didier, Hazan, Jamilé, Burgo, Andrea, Verny, Christophe, Koenig, Michel, Labauge, Pierre, Marelli, Cecilia, N’guyen, Karine, Rodriguez, Diana, Belarbi, Soraya, Hamri, Abdelmadjid, Tazir, Meriem, Boesch, Sylvia, Pandolfo, Massimo, Laura, Jardim, Guergueltcheva, Velina, Tournev, Ivalo, Pedraza Linarès, Olga Lucia, Nielsen, Jørgen E., Svenstrup, Kirsten, Zaki, Maha, Bauer, Peter, Schöls, Lüdger, Schüle, Rebecca, Lossos, Alexander, Bassi, Maria-Teresa, Basso, Manuela, Bertini, Enrico, Brusco, Alfredo, Casali, Carlo, Casari, Giorgio, Criscuolo, Chiara, Filla, Alessandro, Orsi, Laura, Santorelli, Filippo M., Valente, Enza Maria, Vavla, Marinela, Vazza, Giovanni, Megarbane, André, Benomar, Ali, Kremer, Berry, Van Roon-Mom, Willeke, Roxburgh, Richard, Erichsen, Anne Kjersti, Tallaksen, Chantal, Alonso, Isabel, Coutinho, Paula, Loureiro, José Léal, Sequeiros, Jorge, Salih, Mustapha, Kostic, Vladimir S, Rouco Axpe, Idoia, Elsayed, Liena, Paucar, Martin Arce, Roumani, Samir, Bing-Wen, Soong, Reid, Evan, Suran, Nethisinghe, Warner, Thomas, Wood, Nicholas
Published in Genetics in medicine (01.10.2021)
Published in Genetics in medicine (01.10.2021)
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Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel
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
Published in Frontiers in neurology (31.10.2017)
Published in Frontiers in neurology (31.10.2017)
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Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study
Cheikh, Amine, Ajaja, Mohamed Rida, Rhazali, Hicham, Bouatia, Mustapha, Benomar, Ali, Slaoui, Anas, Cherrah, Yahia, Abouqal, Redouane, El Hassani, Amine, Cheikhaoui, Younes
Published in BMC cardiovascular disorders (16.05.2019)
Published in BMC cardiovascular disorders (16.05.2019)
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Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat
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
Published in Frontiers in neurology (31.07.2018)
Published in Frontiers in neurology (31.07.2018)
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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
Mandel, Jean-Louis, David, Gilles, Abbas, Nacer, Dürr, Alexandra, Brice, Alexis, Saudou, Frédéric, Stevanin, Giovanni, Yvert, Gaël, Weber, Chantal, Gemmill, Robert, Drabkin, Harry, Cancel, Géraldine, Agid, Yves, Giunti, Paola, Ruberg, Merle, Imbert, Georges, Benomar, Ali, Antoniou, Eric, Wood, Nick
Published in Nature genetics (01.09.1997)
Published in Nature genetics (01.09.1997)
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Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing
El Fahime, Elmostafa, Yahyaoui, Mohamed, Bouslam, Naima, Smaili, Imane, Jiddane, Mohammed, Kriouale, Yamna, Tibar, Houyam, Bouhouche, Ahmed, Benomar, Ali
Published in Case reports in genetics (2018)
Published in Case reports in genetics (2018)
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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)
Bouslam, Naima, Benomar, Ali, Azzedine, Hamid, Bouhouche, Ahmed, Namekawa, Michito, Klebe, Stephan, Charon, Céline, Durr, Alexandra, Ruberg, Merle, Brice, Alexis, Yahyaoui, Mohamed, Stevanin, Giovanni
Published in Annals of neurology (01.04.2005)
Published in Annals of neurology (01.04.2005)
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Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features
Dürr, A, Stevanin, G, Cancel, G, Duyckaerts, C, Abbas, N, Didierjean, O, Chneiweiss, H, Benomar, A, Lyon-Caen, O, Julien, J, Serdaru, M, Penet, C, Agid, Y, Brice, A
Published in Annals of neurology (01.04.1996)
Published in Annals of neurology (01.04.1996)
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An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3
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
Published in BMC genetics (21.03.2012)
Published in BMC genetics (21.03.2012)
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Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families
ELLEUCH, Nizar, BOUSLAM, Naima, BACQ, Delphine, TAZIR, Meriem, ZELENIKA, Diana, ARGOV, Zohar, DURR, Alexandra, YAHYAOUI, Mohamed, BENOMAR, Ali, BRICE, Alexis, STEVANIN, Giovanni, HANEIN, Sylvain, LOSSES, Alexander, HAMRI, Abdelmadjid, KLEBE, Stephan, MEINER, Vardiella, BIROUK, Nezha, LERER, Israela, GRID, Djamel
Published in Neurogenetics (01.11.2007)
Published in Neurogenetics (01.11.2007)
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Efficacy and Safety in Patients with Multiple Sclerosis Treated with Ocrelizumab
Moufakkir, Rim, Tibar, Houyam, Nassiri, Hajar, Regragui, Wafa, Benomar, Ali
Published in Multiple sclerosis and related disorders (01.12.2023)
Published in Multiple sclerosis and related disorders (01.12.2023)
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The Use of Rituximab in the Treatment of Multiple Sclerosis in Morrocco
Siham, Asri, Houyam, Tibar, Amal, Souidi, Ali, Benomar, Wafaa, Regragui
Published in Multiple sclerosis and related disorders (01.03.2023)
Published in Multiple sclerosis and related disorders (01.03.2023)
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