A DNA methylation signature discriminates between excellent and non-response to lithium in patients with bipolar disorder type 1 von Marie-Claire, C., Lejeune, F. X., Mundwiller, E., Ulveling, D., Moszer, I., Bellivier, F., Etain, B.

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SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum von Goizet, C, Boukhris, A, Maltete, D, Guyant-Maréchal, L, Truchetto, J, Mundwiller, E, Hanein, S, Jonveaux, P, Roelens, F, Loureiro, J, Godet, E, Forlani, S, Melki, J, Auer-Grumbach, M, Fernandez, J C, Martin-Hardy, P, Sibon, I, Sole, G, Orignac, I, Mhiri, C, Coutinho, P, Durr, A, Brice, A, Stevanin, G

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PO19-WE-05 Linkage analysis and mutation screening in PANK2 and PLA2G6 genes in 7 consanguineous Saudi Arabian families with Karak syndrome von Azzedine, H, Salih, M.A.M, Khan, A, Mundwiller, E, Aldriss, A, Elmalik, S.A, Kabiraj, M.M, Stevanin, G

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Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds von Bauer, Peter, Stevanin, Giovanni, Beetz, Christian, Synofzik, Matthis, Schmitz-Hübsch, Tanja, Wüllner, Ullrich, Berthier, Eric, Ollagnon-Roman, Elisabeth, Riess, Olaf, Forlani, Sylvie, Mundwiller, Emeline, Durr, Alexandra, Schöls, Ludger, Brice, Alexis

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Combination of Positional Cloning and New Generation Sequencing Identifies 3 Novel Genes in Spastic Paraplegia Involved in Common Metabolic Pathways (P01.205) von Stevanin, G., Tesson, C., Nawara, M., Salih, M., Zaki, M., Mundwiller, E., Al Balwi, M., Boukhris, A., Bouhouche, A., Martin, E., Elmalik, S., Alswaid, A., Mochel, F., Santorelli, F., Benomar, A., Al Rasheed, S., Mhiri, C., Gleeson, J., Darios, F., Durr, A., Brice, A.

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SPG 15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum von GOIZET, C, BOUKHRIS, A, GODET, E, FORLANI, S, MELKI, J, AUER-GRUMBAEH, M, FERNANDEZ, J. C, MARTIN-HARDY, P, SIBON, I, SOLE, G, ORIGNAC, I, MHIRI, C, MALTETE, D, COUTINHO, P, DURR, A, BRICE, A, STEVANIN, G, GUYANT-MARECHAL, L, TRUCHETTO, J, MUNDWILLER, E, HANEIN, S, JONVEAUX, P, ROELENS, F, LOUREIRO, J

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KIF1A missense mutations in SPG30: Distinct phenotypes according to the nature of the mutations von Klebe, S., Lossos, A., Azzedine, H., Mundwiller, E., Meiner, V., Gaussen, M., Marelli, C., Nawara, M., Carpentier, W., Meyer, V., Raststetter, A., Martin, E., Orlando, L., Gyapay, G., El-Hachimi, K., Zimmermann, B., Lerer, I., Brice, A., Durr, A., Stevanin, G.

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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations von KLEBEL, Stephan, LOSSOS, Alexander, RASTETTER, Agnes, MARTIN, Elodie, BOUTEILLER, Delphine, ORLANDO, Laurent, GYAPAY, Gabor, EL-HACHIMI, Khalid H, ZIMMERMAN, Batel, GAMLIEL, Moriya, MISK, Adel, LERER, Israela, AZZEDINE, Hamid, BRICE, Alexis, DURR, Alexandra, STEVANIN, Giovanni, MUNDWILLER, Emeline, SHEFFER, Ruth, GAUSSEN, Marion, MARELLI, Cecilia, NAWARA, Magdalena, CARPENTIER, Wassila, MEYER, Vincent

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DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy von Picard, Fabienne, Makrythanasis, Periklis, Navarro, Vincent, Ishida, Saeko, de Bellescize, Julitta, Ville, Dorothée, Weckhuysen, Sarah, Fosselle, Erwin, Suls, Arvid, De Jonghe, Peter, Vasselon Raina, Maryline, Lesca, Gaetan, Depienne, Christel, An-Gourfinkel, Isabelle, Vlaicu, Mihaela, Baulac, Michel, Mundwiller, Emeline, Couarch, Philippe, Combi, Romina, Ferini-Strambi, Luigi, Gambardella, Antonio, Antonarakis, Stylianos E, Leguern, Eric, Steinlein, Ortrud, Baulac, Stéphanie

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Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25 von Barbier, Mathieu, Bahlo, Melanie, Pennisi, Alessandra, Jacoupy, Maxime, Tankard, Rick M., Ewenczyk, Claire, Davies, Kayli C., Lino‐Coulon, Patricia, Colace, Claire, Rafehi, Haloom, Auger, Nicolas, Ansell, Brendan R. E., Stelt, Ivo, Howell, Katherine B., Coutelier, Marie, Amor, David J., Mundwiller, Emeline, Guillot‐Noël, Lena, Storey, Elsdon, Gardner, R. J. McKinlay, Wallis, Mathew J., Brusco, Alfredo, Corti, Olga, Rötig, Agnès, Leventer, Richard J., Brice, Alexis, Delatycki, Martin B., Stevanin, Giovanni, Lockhart, Paul J., Durr, Alexandra

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