Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients von Tibar, Houyam, El Bayad, Khalil, Bouhouche, Ahmed, Ait Ben Haddou, El Hachmia, Benomar, Ali, Yahyaoui, Mohamed, Benazzouz, Abdelhamid, Regragui, Wafa

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Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment von 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

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Headache and Status Epilepticus Reveal Paget's Disease of the Bone von Ouhabi, Dahab, Tibar, Houyam, Benomar, Ali, Jiddane, Mohamed, Regragui, Wafa

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Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome von 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

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Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease von Smaili, Imane, Tesson, Christelle, Regragui, Wafa, Bertrand, Hélène, Rahmani, Mounia, Bouslam, Naima, Benomar, Ali, Brice, Alexis, Lesage, Suzanne, Bouhouche, Ahmed

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

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

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Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment von 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

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A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis von Aasfara, Jehanne, Regragui, Wafa, Ouardi, Loubna El, Haddou, El Hachmia Ait Ben, Benomar, Ali, Yahyaoui, Mohammed

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Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel von 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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Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study von Cheikh, Amine, Ajaja, Mohamed Rida, Rhazali, Hicham, Bouatia, Mustapha, Benomar, Ali, Slaoui, Anas, Cherrah, Yahia, Abouqal, Redouane, El Hassani, Amine, Cheikhaoui, Younes

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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion von David, Gilles, Abbas, Nacer, Stevanin, Giovanni, Dürr, Alexandra, Yvert, Gaël, Cancel, Géraldine, Weber, Chantal, Imbert, Georges, Saudou, Frédéric, Antoniou, Eric, Drabkin, Harry, Gemmill, Robert, Giunti, Paola, Benomar, Ali, Wood, Nick, Ruberg, Merle, Agid, Yves, Mandel, Jean-Louis, Brice, Alexis

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Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat von 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

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

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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) von Bouslam, Naima, Benomar, Ali, Azzedine, Hamid, Bouhouche, Ahmed, Namekawa, Michito, Klebe, Stephan, Charon, Céline, Durr, Alexandra, Ruberg, Merle, Brice, Alexis, Yahyaoui, Mohamed, Stevanin, Giovanni

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Spinocerebellar ataxia 3 and machado-joseph disease: Clinical, molecular, and neuropathological features von Durr, Alexandra, Stevanin, Giovanni, Cancel, Geraldine, Duyckaerts, Charles, Abbas, Nacer, Didierjean, Olivier, Chneiweiss, Herve, Benomar, Ali, Lyon-Caen, Olivier, Julien, Jean, Serdaru, Michel, Penet, Christiane, Agid, Yves, Brice, Alexis

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Efficacy and Safety in Patients with Multiple Sclerosis Treated with Ocrelizumab von Moufakkir, Rim, Tibar, Houyam, Nassiri, Hajar, Regragui, Wafa, Benomar, Ali

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The Use of Rituximab in the Treatment of Multiple Sclerosis in Morrocco von Siham, Asri, Houyam, Tibar, Amal, Souidi, Ali, Benomar, Wafaa, Regragui

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Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders von 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, Mahmoud, Iman Gamal El Din, 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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Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes von Coutelier, Marie, Hammer, Monia B, Stevanin, Giovanni, Monin, Marie-Lorraine, Davoine, Claire-Sophie, Mochel, Fanny, Labauge, Pierre, Ewenczyk, Claire, Ding, Jinhui, Gibbs, J. Raphael, Hannequin, Didier, Melki, Judith, Toutain, Annick, Laugel, Vincent, Forlani, Sylvie, Charles, Perrine, Broussolle, Emmanuel, Thobois, Stéphane, Afenjar, Alexandra, Anheim, Mathieu, Calvas, Patrick, Castelnovo, Giovanni, de Broucker, Thomas, Vidailhet, Marie, Moulignier, Antoine, Ghnassia, Robert T, Tallaksen, Chantal, Mignot, Cyril, Goizet, Cyril, Le Ber, Isabelle, Ollagnon-Roman, Elisabeth, Pouget, Jean, Brice, Alexis, Singleton, Andrew, Durr, Alexandra

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