Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update by Tazir, Meriem, Hamadouche, Tarik, Nouioua, Sonia, Mathis, Stephane, Vallat, Jean-Michel

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Characterization of Recessive Parkinson Disease in a Large Multicenter Study by Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Romdhan, Sawssan Ben, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Toullec, Benjamin Le, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohamed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Ben Romdhan, Sawssan, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Le Toullec, Benjamin, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Ben Djebara, Mouna, Gouider, Riadh, Tazir, Meriem, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andy, Corvol, Jean‐Christophe, Brice, Alexis

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Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism by Fiskerstrand, Torunn, H'mida-Ben Brahim, Dorra, Johansson, Stefan, M'zahem, Abderrahim, Haukanes, Bjørn Ivar, Drouot, Nathalie, Zimmermann, Julian, Cole, Andrew J., Vedeler, Christian, Bredrup, Cecilie, Assoum, Mirna, Tazir, Meriem, Klockgether, Thomas, Hamri, Abdelmadjid, Steen, Vidar M., Boman, Helge, Bindoff, Laurence A., Koenig, Michel, Knappskog, Per M.

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DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study by Trinh, Joanne, BSc, Gustavsson, Emil K, MSc, Vilariño-Güell, Carles, PhD, Bortnick, Stephanie, BSc, Latourelle, Jeanne, PhD, McKenzie, Marna B, BSc, Tu, Chelsea Szu, MSc, Nosova, Ekaterina, PhD, Khinda, Jaskaran, BSc, Milnerwood, Austen, PhD, Lesage, Suzanne, PhD, Brice, Alexis, MD, Tazir, Meriem, MD, Aasly, Jan O, MD, Parkkinen, Laura, PhD, Haytural, Hazal, MSc, Foroud, Tatiana, PhD, Myers, Richard H, PhD, Sassi, Samia Ben, MD, Hentati, Emna, MD, Nabli, Fatma, MD, Farhat, Emna, MD, Amouri, Rim, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, Dr

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Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case report by Kediha, Mohamed Islam, Tazir, Meriem, Sternberg, Damien, Eymard, Bruno, Alipacha, Lamia

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Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes by Tazir, Meriem, Bellatache, Mounia, Nouioua, Sonia, Vallat, Jean-Michel

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NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study by Echaniz-Laguna, Andoni, Altuzarra, Cecilia, Verloes, Alain, De La Banda, Marta Gomez Garcia, Quijano-Roy, Susana, Tudorache, Raluca Anca, Jaxybayeva, Altynshash, Myrzaliyeva, Bakhytkul, Tazir, Meriem, Vallat, Jean-Michel, Francou, Bruno, Urtizberea, Jon Andoni

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Distal hereditary motor neuropathies by Tazir, Meriem, Nouioua, Sonia

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Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse by De Sandre-Giovannoli, Annachiara, Chaouch, Malika, Kozlov, Serguei, Vallat, Jean-Michel, Tazir, Meriem, Kassouri, Nadia, Szepetowski, Pierre, Hammadouche, Tarik, Vandenberghe, Antoon, Stewart, Colin L., Grid, Djamel, Lévy, Nicolas

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Beyond the disability, what is the quality of life in Algerian patients with multiple sclerosis? by Hecham, Nassima, Tazir, Meriem, Pacha, Lamia Ali

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The methylenetetrahydrofolate reductase C677T and A1298C genetic polymorphisms and plasma homocysteine in Alzheimer's disease in an Algerian population by Bouguerra, Khadidja, Tazir, Meriem, Melouli, Hamid, Khelil, Malika

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Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes by Nouioua, Sonia, Hamadouche, Tarik, Funalot, Benoit, Bernard, Rafaëlle, Bellatache, Nora, Bouderba, Radia, Grid, Djamel, Assami, Salima, Benhassine, Traki, Levy, Nicolas, Vallat, Jean-Michel, Tazir, Meriem

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Les comorbidités non psychiatriques associées à la sclérose en plaques : à propos d’une cohorte algérienne by Hecham, Nassima, Tazir, Meriem

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Intragenic deletion patterns of dystrophin gene in Duchenne and Becker muscular dystrophy patients from Algeria by Cherrallah, Amira, Benhassine, Traki, Nouioua, Sonia, Makri, Samira, Chaouch, Malika, Tazir, Meriem, Hamadouche, Tarik

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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders by Salpietro, Vincenzo, Dixon, Christine L., Guo, Hui, Bello, Oscar D., Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Heimer, Gali, Burglen, Lydie, Valence, Stephanie, Torti, Erin, Hacke, Moritz, Rankin, Julia, Tariq, Huma, Colin, Estelle, Procaccio, Vincent, Striano, Pasquale, Mankad, Kshitij, Lieb, Andreas, Chen, Sharon, Pisani, Laura, Bettencourt, Conceicao, Männikkö, Roope, Manole, Andreea, Brusco, Alfredo, Grosso, Enrico, Ferrero, Giovanni Battista, Armstrong-Moron, Judith, Gueden, Sophie, Bar-Yosef, Omer, Tzadok, Michal, Monaghan, Kristin G., Santiago-Sim, Teresa, Person, Richard E., Cho, Megan T., Willaert, Rebecca, Yoo, Yongjin, Chae, Jong-Hee, Quan, Yingting, Wu, Huidan, Wang, Tianyun, Bernier, Raphael A., Xia, Kun, Blesson, Alyssa, Jain, Mahim, Motazacker, Mohammad M., Jaeger, Bregje, Schneider, Amy L., Boysen, Katja, Muir, Alison M., Myers, Candace T., Gavrilova, Ralitza H., Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W., Dyment, David, Osmond, Matthew, Parellada, Mara, Llorente, Cloe, Gonzalez-Peñas, Javier, Carracedo, Angel, Van Haeringen, Arie, Ruivenkamp, Claudia, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Minetti, Carlo, Skabar, Aldo, Fabretto, Antonella, Raspall-Chaure, Miquel, Chez, Michael, Tsai, Anne, Fassi, Emily, Shinawi, Marwan, Constantino, John N., De Zorzi, Rita, Fortuna, Sara, Kok, Fernando, Keren, Boris, Bonneau, Dominique, Choi, Murim, Benzeev, Bruria, Zara, Federico, Mefford, Heather C., Scheffer, Ingrid E., Clayton-Smith, Jill, Macaya, Alfons, Rothman, James E., Eichler, Evan E., Kullmann, Dimitri M., Houlden, Henry

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Moderate phenotype of a congenital myasthenic syndrome type 19 in an Algerian patient by Kediha, Mohamed Islam, Tazir, Meriem, Sternberg, Damien, Eymard, Bruno, Pacha, Lamia Ali

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Familial and sporadic forms of MS in Algeria: Are there distinctive clinical and genetic features? by Hecham, Nassima, Tazir, Meriem, Boudjella, Mohamed Lotfi, Benhalima, Malika, Pacha, Lamia Ali

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Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go by Dangouloff, Tamara, Vrščaj, Eva, Servais, Laurent, Osredkar, Damjan, Adoukonou, Thierry, Aryani, Omid, Barisic, Nina, Bashiri, Fahad, Bastaki, Laila, Benitto, Afaf, Omran, Tawfeg Ben, Bernert, Guenther, Bertini, Enrico, Borde, Patricia, Born, Peter, Boustani, Rose-Mary, Butoianu, Nina, Castiglioni, Claudia, Catibusic, Feriha, Chan, Sophelia, Chien, Yin Hsiu, Christodoulou, Kyproula, Dejsuphong, Donniphat, Farrar, Michelle, Filip, Duma, Goemans, Nathalie, Guinhouya, Kokou, Haberlova, Jana, Hadzsiev, Kinga, Hovhannesyan, Kristine, Isohanni, Pirjo, Radovic, Nelica Ivanovic, Jacquier, David, Jalloh, Alusine, Jedrzejowska, Maria, Kandawasvika, Gwen, Kaputu, Celestin, Kawatu, Nfwama, Kernohan, Kristin, Kirschner, Jan, Klink, Barbara, Kodsy, Sherry, Kouame-Assouan, Ange-Eric, Kravljanac, Ruzica, Kreile, Madara, Litvinenko, Ivan, McMillan, Hugh, Mesa, Sandra, Mohamed, Inaam, Kanzoska, Liljana Muaremoska, Nevo, Yoram, Nguefack, Seraphin, Nkole, Kafula, O'Grady, Gina, O'Rourke, Declan, Oskoui, Maryam, Piazzon, Flavia, Poddighe, Dimitri, Prasauskiene, Audrone, Prieto, Juan, Rasmussen, Magnhild, Razafindrasata, Santara, Saha, Narayan, Saito, Kayoko, Sakadi, Foksouna, Sangare, Modibo, Schroth, Mary, Shalkevich, Leanid, Shatillo, Andriy, Suthar, Renu, Szabo, Lena, Tatishvili, Nana, Tazir, Meriem, Tizzano, Eduardo, Topaloglu, Haluk, Tulinius, Mar, van der Pol, Ludo, Vazquez, Gabriel, Vlodavets, Dimitry, Wanigasinghe, Jithangi, Wilmshurst, Jo, Xiong, Hui, Zafeiriou, Dimitrios, Zamba, Eleni

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Nonsteroidal Anti‐inflammatory Use and LRRK2 Parkinson's Disease Penetrance by San Luciano, Marta, Tanner, Caroline M., Meng, Cheryl, Marras, Connie, Lang, Anthony E., Schüle, Birgitt, Langston, J. William, Corvol, Jean‐Christophe, Goldwurm, Stefano, Berg, Daniela, Tazir, Meriem, Mellick, George D., Sue, Carolyn M., Tan, Eng King, Bressman, Susan, Saunders‐Pullman, Rachel, Raymond, Deborah, Barrett, Matthew James, Cabassa, Jose, Groves, Mark, Hunt, Ann L, Lubarr, Naomi, Palmese, Christina, Sachdev, Rivka, Sarva, Harini, Shanker, Vicki, Swan, Matthew Carrington, Soto‐Valencia, Jeannie, Johannes, Brooke, Ortega, Robert, Alcalay, Roy N, Tang, Ming‐X, Santana, Helen Mejia, Orbe‐Reilly, Martha, Fahn, Stanley, Cote, Lucien, Ford, Blair, Louis, Elan, Levy, Oren, Rosado, Llency, Ruiz, Diana, Clark, Lorraine, Marder, Karen S, Corvol, Jean‐Christophe, Bonnet, Anne‐Marie, Welter, Marie‐Laure, Mesnage, Valerie, Vidailhet, Marie, Roze, Emmanuel, Lacomblez, Lucette, Grabli, David, Mart i Masso, Jose Felix, Mondragon Rezola, Elisabet, Alustiza, Ainara Estanga, Pagola, Ana Gorostidi, Pont‐Sunyer, Claustre, Rolan, Dolores Vilas, Fernandez‐Santiago, Ruben, Quintana, Maria, Maragall, Laura, Hentati, Faycal, Farrer, Matthew, Duda, John, Read, Matt, Gibson, Rachel, Sassi, Samia Ben, Zouari, Mourad, Nabli, Fatma, Aasly, Jan, Andersen, Sigrid, Bertoni, John, Carter, Julie, Elmer, Lawrence, Jimenez, Nestor Galvez, Martin, Wayne, Pahwa, Rajesh, Lyons, Kelly, Reich, Stephen, Ramos, Carmen Serrano, Wojcieszek, Joanne, Gurevich, Tanya, Shira, Anat Bar, Weisz, Mali Gana, Yasinovsky, Kira, Zalis, Maayan, Thaler, Avner, Orr‐Urtreger, Avi, Giladi, Nir, Mountain, Joanna, Mestre, Tiago, Ghate, Taneera, Singerman, Jennifer, Al Dakheel, Amaal, Connolly, Barbara S, Gasser, Thomas, Brockmann, Kathrin, Mullins, Meghan E, Northover, Carrie, Facheris, Maurizio, Fiske, Brian

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Hereditary peripheral neuropathies by Vallat, Jean-Michel, Tazir, Mériem, Calvo, Judith, Funalot, Benoît

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