Thrombophlébite cérébrale : penser à l’hyperthyroïdie von Rivoisy, C., Desforges, V., Tir, M., Chaouch, R.B., Bédos, J.-P., Béressi, J.-P., Bruneel, F.

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Cerebral venous thrombosis: look for hyperthyroidism von Rivoisy, C, Desforges, V, Tir, M, Chaouch, R B, Bédos, J-P, Béressi, J-P, Bruneel, F

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What is your diagnosis? Colonic duplication, noncommunicating, calcified von Chaouch, R B, Merzoug, V, Wann, A R, Adamsbaum, C

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Quel est votre diagnostic ? von Chaouch, R.B., Merzoug, V., Wann, A.R., Adamsbaum, C.

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Cerebral venous thrombosis: look for hyperthyroidism von Rivoisy, C, Desforges, V, Tir, M, Chaouch, R B, Bédos, J-P, Béressi, J-P, Bruneel, F

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Clinical trials in amyotrophic lateral sclerosis: a systematic review and perspective von Wong, Charis, Stavrou, Maria, Elliott, Elizabeth, Gregory, Jenna M, Leigh, Nigel, Pinto, Ashwin A, Williams, Timothy L, Chataway, Jeremy, Swingler, Robert, Parmar, Mahesh K B, Stallard, Nigel, Weir, Christopher J, Parker, Richard A, Chaouch, Amina, Hamdalla, Hisham, Ealing, John, Gorrie, George, Morrison, Ian, Duncan, Callum, Connelly, Peter, Carod-Artal, Francisco Javier, Davenport, Richard, Reitboeck, Pablo Garcia, Radunovic, Aleksandar, Srinivasan, Venkataramanan, Preston, Jenny, Mehta, Arpan R, Leighton, Danielle, Glasmacher, Stella, Beswick, Emily, Williamson, Jill, Stenson, Amy, Weaver, Christine, Newton, Judith, Lyle, Dawn, Dakin, Rachel, Macleod, Malcolm, Pal, Suvankar, Chandran, Siddharthan

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Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders von Travaglini, Lorena, Brancati, Francesco, Silhavy, Jennifer, Iannicelli, Miriam, Nickerson, Elizabeth, Elkhartoufi, Nadia, Scott, Eric, Spencer, Emily, Gabriel, Stacey, Thomas, Sophie, Ben-Zeev, Bruria, Bertini, Enrico, Boltshauser, Eugen, Chaouch, Malika, Cilio, Maria Roberta, de Jong, Mirjam M, Kayserili, Hulya, Ogur, Gonul, Poretti, Andrea, Signorini, Sabrina, Uziel, Graziella, Zaki, Maha S, Johnson, Colin, Attié-Bitach, Tania, Gleeson, Joseph G, Valente, Enza Maria

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Association of an HLA-G 14-bp Insertion/Deletion polymorphism with high HBV replication in chronic hepatitis von Laaribi, A. B., Zidi, I., Hannachi, N., Ben Yahia, H., Chaouch, H., Bortolotti, D., Zidi, N., Letaief, A., Yacoub, S., Boudabous, A., Rizzo, R., Boukadida, J.

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HLA-E polymorphism and soluble HLA-E plasma levels in chronic hepatitis B patients von Zidi, I., Laaribi, A. B., Bortolotti, D., Belhadj, M., Mehri, A., Yahia, H. B., Babay, W., Chaouch, H., Zidi, N., Letaief, A., Yacoub, S., Boukadida, J., Di Luca, D., Hannachi, N., Rizzo, R.

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Cs2[M(H2O)6]3(HPO3)4, M = Co, Ni: Crystal structures, IR and thermal studies von Chaouch, S, Ouarsal, R, Akouibaa, M, Rakib, S, Lachkar, M, El Bali, B, Dusek, M

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Cs 2 [M(H 2 O) 6 ] 3 (HPO 3 ) 4 , M = Co, Ni: Crystal structures, IR and thermal studies von Chaouch, S, Ouarsal, R, Akouibaa, M, Rakib, S, Lachkar, M, El Bali, B, Dusek, M

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Galanin pathogenic mutations in temporal lobe epilepsy von Guipponi, Michel, Chentouf, Amina, Webling, Kristin E B, Freimann, Krista, Crespel, Arielle, Nobile, Carlo, Lemke, Johannes R, Hansen, Jörg, Dorn, Thomas, Lesca, Gaetan, Ryvlin, Philippe, Hirsch, Edouard, Rudolf, Gabrielle, Rosenberg, Dominique Sarah, Weber, Yvonne, Becker, Felicitas, Helbig, Ingo, Muhle, Hiltrud, Salzmann, Annick, Chaouch, Malika, Oubaiche, Mohand Laid, Ziglio, Serena, Gehrig, Corinne, Santoni, Federico, Pizzato, Massimo, Langel, Ülo, Antonarakis, Stylianos E

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Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations von Guergueltcheva, Velina, Müller, Juliane S., Dusl, Marina, Senderek, Jan, Oldfors, Anders, Lindbergh, Christopher, Maxwell, Susan, Colomer, Jaume, Mallebrera, Cecilia Jimenez, Nascimento, Andres, Vilchez, Juan J., Muelas, Nuria, Kirschner, Janbernd, Nafissi, Shahriar, Kariminejad, Ariana, Nilipour, Yalda, Bozorgmehr, Bita, Najmabadi, Hossein, Rodolico, Carmelo, Sieb, Jörn P., Schlotter, Beate, Schoser, Benedikt, Herrmann, Ralf, Voit, Thomas, Steinlein, Ortrud K., Najafi, Abdolhamid, Urtizberea, Andoni, Soler, Doriette M., Muntoni, Francesco, Hanna, Michael G., Chaouch, Amina, Straub, Volker, Bushby, Kate, Palace, Jacqueline, Beeson, David, Abicht, Angela, Lochmüller, Hanns

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Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia von Kalai, M, Chaouch, L, Mansour, I B, Hafsia, R, Ghanem, A, Abbes, S

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Estimating ground motion incoherence through finite source simulation: a case study of the 1980 El-Asnam Earthquake von AfifChaouch, K., Tiliouine, B., Hammoutene, M., Sigbjörnsson, R., Rupakhety, R.

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Impact of Genetic and Nongenetic Factors on Body Mass Index and Waist-Hip Ratio Change in HIV-Infected Individuals Initiating Antiretroviral Therapy von Barceló, Catalina, Guidi, Monia, Thorball, Christian W, Hammer, Christian, Chaouch, Aziz, Scherrer, Alexandra U, Hasse, Barbara, Cavassini, Matthias, Furrer, Hansjakob, Calmy, Alexandra, Haubitz, Sebastian, Bernasconi, Enos, Buclin, Thierry, Fellay, Jacques, Tarr, Philip E, Csajka, Chantal

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G.O.4 Search for SNPs modifiers in DMD with different corticosteroids response by candidate genes targeted resequencing von Bovolenta, M, Sartori, A, Rieber, N, Scapoli, C, Zaharieva, I, t’Hoen, P.B, Chaouch, A, Merlini, L, Bertini, E, Mercuri, E, Kotelnikova, E, Schwartz, E, Cirak, S, Morgan, J, Tanzi, R, Lochmueller, H, Muntoni, F, Ferlini, A

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Minimizing cost of continuous audit: Counting and time dependent strategies von Pathak, Jagdish, Chaouch, Ben, Sriram, Ram S.

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A randomized double-blind clinical trial on safety and efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment in patients affected by amyotrophic lateral sclerosis (ALS)... von Lombardo, F.L, Spila Alegiani, S, Mayer, F, Cipriani, M, Lo Giudice, M, Ludolph, A.C, McDermott, C.J, Corcia, P, Van Damme, P, Van den Berg, L.H, Hardiman, O, Nicolini, G, Vanacore, N, Dickie, B, Albanese, A, Puopolo, M, Tornese, P, Cocco, A, Matteoli, M, Lauranzano, E, Malosio, M.L, Elia, C.A, Chiò, A, Manera, U, Moglia, C, Calvo, A, Salamone, P, Fuda, G, Colosimo, C, Spera, C, Ranchicchio, P.C, Stipa, G, Frondizi, D, Lunetta, C, Sansone, V, Tarlarini, C, Gerardi, F, Silani, V, Doretti, A, Colombo, E, Demirtzidis, G, Tedeschi, G, Trojsi, F, Passaniti, C, Ballestrero, S, Dorst, J, Weiland, U, Fromm, A, Wiesenfarth, M, Kandler, K, Witzel, S, Otto, M, Schuster, J, Meyer, T, Maier, A, Kettemann, D, Petri, S, Müschen, L, Wohnrade, C, Sarikidi, A, Osmanovic, A, Grosskreutz, J, Rödiger, A, Steinbach, R, Ilse, B, Smesny, U, Untucht, R, Günther, R, Vidovic, M, Shaw, P, Collins, A, Wollff, H, Walsh, T, Tuddenham, L, Kazoka, M, White, D, Young, S, Thompson, B, Madarshahian, D, Chhetri, S.K, Chaouch, A, Young, C.A, Arndt, H, Hanemann, C, Lambert, T, Beltran, S, Couratier, P, Esselin, F, Camu, W, De La Cruz, E, Lemasson, G, Masrori, P, Maguire, S, Fogarty, L, Atoyebi, T, Obáin, N.N

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Posterior scleritis: six case reports von Ladjimi, A, Messaoud, R, Attia, S, Jenzri, S, Zaouali, S, Chaouch, K, Bhouri, L, Jelliti, B, Khairallah, M

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