Serum neurofilament light chain at time of diagnosis is an independent prognostic factor of survival in amyotrophic lateral sclerosis von Thouvenot, E., Demattei, C., Lehmann, S., Maceski‐Maleska, A., Hirtz, C., Juntas‐Morales, R., Pageot, N., Esselin, F., Alphandéry, S., Vincent, T., Camu, W.

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An amyotrophic lateral sclerosis hot spot in the French Alps associated with genotoxic fungi von Lagrange, E., Vernoux, J.P., Reis, J., Palmer, V., Camu, W., Spencer, P.S.

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Therapeutic tools for familial ALS von Camu, W., De La Cruz, E., Esselin, F.

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ALS and environment: Clues from spatial clustering? von Spencer, P.S., Lagrange, E., Camu, W.

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Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis von Daoud, H, Valdmanis, P N, Kabashi, E, Dion, P, Dupré, N, Camu, W, Meininger, V, Rouleau, G A

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Chitinase 3-like proteins as diagnostic and prognostic biomarkers of multiple sclerosis von Hinsinger, G, Galéotti, N, Nabholz, N, Urbach, S, Rigau, V, Demattei, C, Lehmann, S, Camu, W, Labauge, P, Castelnovo, G, Brassat, D, Loussouarn, D, Salou, M, Laplaud, D, Casez, O, Bockaert, J, Marin, P, Thouvenot, E

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Autosomal dominant SPG9: intrafamilial variability and onset during pregnancy von Marelli, C., Badiou, S., Genestet, S., Larrieu, L., Damier, P., Camu, W., Planes, M., Koenig, M., Guissart, C.

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Vitamin D is associated with degree of disability in patients with fully ambulatory relapsing-remitting multiple sclerosis von Thouvenot, E., Orsini, M., Daures, J.-P., Camu, W.

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Pre-symptomatic diagnosis in ALS von Corcia, P., Lumbroso, S., Cazeneuve, C., Mouzat, K., Camu, W., Vourc’h, P.

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Neuromyelitis optica in France: A multicenter study of 125 patients von COLLONGUES, N, MARIGNIER, R, FONTAINE, B, BRASSAT, D, CLANET, M, MILH, M, PELLETIER, J, AUDOIN, B, RUET, A, LEBRUN-FRENAY, C, THOUVENOT, E, CAMU, W, ZEPHIR, H, DEBOUVERIE, M, CREANGE, A, MOREAU, T, LABAUGE, P, CASTELNOVO, G, EDAN, G, LE PAGE, E, DEFER, G, BARROSO, B, HEINZLEF, O, PAPEIX, C, GOUT, O, RODRIGUEZ, D, WIERTLEWSKI, S, LAPLAUD, D, BORGEL, F, TOURNIAIRE, P, GRIMAUD, J, BROCHET, B, VERMERSCH, P, CONFAVREUX, C, BLANC, F, DE SEZE, J, RITLENG, C, TCHIKVILADZE, M, OUTTERYCK, O, VUKUSIC, S, FLEURY, M

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Mutations in FUS cause FALS and SALS in French and French Canadian populations von BELZIL, V. V, VALDMANIS, P. N, LACOMBLEZ, L, SALACHAS, F, PRADAT, P.-F, CAMU, W, MEININGER, V, DUPRE, N, ROULEAU, G. A, DION, P. A, DAOUD, H, KABASHI, E, NOREAU, A, GAUTHIER, J, HINCE, P, DESJARLAIS, A, BOUCHARD, J.-P

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Adult-onset spinal muscular atrophy: An update von Juntas Morales, R., Pageot, N., Taieb, G., Camu, W.

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Long-term follow-up of neuromyelitis optica with a pediatric onset von COLLONGUES, N, MARIGNIER, R, AUDOIN, B, THOUVENOT, E, CAMU, W, BARROSO, B, RUET, A, BROCHET, B, VERMERSCH, P, CONFAVREUX, C, DE SEZE, J, ZEPHIR, H, PAPEIX, C, FONTAINE, B, BLANC, F, RODRIGUEZ, D, FLEURY, M, VUKUSIC, S, PELLETIER, J

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Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations von CORCIA, P, VALDMANIS, P, DANEL-BRUNAUD, V, VANDENBERGHE, N, PRADAT, P. F, COURATIER, P, SALACHAS, F, LUMBROSO, S, ROULEAU, G. A, MEININGER, V, CAMU, W, MILLECAMPS, S, LIONNET, C, BLASCO, H, MOUZAT, K, DAOUD, H, BELZIL, V, MORALES, R, PAGEOT, N

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Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study von Gil, J., Funalot, B., Verschueren, A., Danel-Brunaud, V., Camu, W., Vandenberghe, N., Desnuelle, C., Guy, N., Camdessanche, J. P., Cintas, P., Carluer, L., Pittion, S., Nicolas, G., Corcia, P., Fleury, M.-C., Maugras, C., Besson, G., Le Masson, G., Couratier, P.

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Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease von LE BER, I, CAMUZAT, A, HEATH, S, CAMU, W, MARTINAUD, O, LACOMBLEZ, L, VERCELLETTO, M, SALACHAS, F, SELLAL, F, DIDIC, M, THOMAS-ANTERION, C, PUEL, M, BERGER, E, MICHEL, B.-F, BESSE, C, DUYCKAERTS, C, MEININGER, V, CAMPION, D, DUBOIS, B, BRICE, A, HANNEQUIN, D, LAQUERRIERE, A, GOLFIER, V, SEILHEAN, D, VIENNET, G, COURATIER, P, VERPILLAT, P

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SOD1 mutation can mask C9orf72 abnormal expansion von Corcia, P., Blasco, H., Besson, G., Camdessanché, J.‐P., Pautot, V., Beltran, S., Couratier, P., Andres, C., Camu, W., Vourc'h, P.

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A prospective observational post-marketing study of natalizumab-treated multiple sclerosis patients: clinical, radiological and biological features and adverse events. The BIONAT c... von Outteryck, O., Ongagna, J.C., Brochet, B., Rumbach, L., Lebrun-Frenay, C., Debouverie, M., Zéphir, H., Ouallet, J.C., Berger, E., Cohen, M., Pittion, S., Laplaud, D., Wiertlewski, S., Cabre, P., Pelletier, J., Rico, A., Defer, G., Derache, N., Camu, W., Thouvenot, E., Moreau, T., Fromont, A., Tourbah, A., Labauge, P., Castelnovo, G., Clavelou, P., Casez, O., Hautecoeur, P., Papeix, C., Lubetzki, C., Fontaine, B., Couturier, N., Bohossian, N., Clanet, M., Vermersch, P., de Sèze, J., Brassat, D.

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SMN1 gene, but not SMN2, is a risk factor for sporadic ALS von CORCIA, P, CAMU, W, HALIMI, J.-M, VOURC'H, P, ANTAR, C, VEDRINE, S, GIRAUDEAU, B, DE TOFFOL, B, ANDRES, C. R

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High-risk syndrome for neuromyelitis optica: a descriptive and comparative study von Collongues, N, Marignier, R, Zéphir, H, Blanc, F, Vukusic, S, Outteryck, O, Fleury, M, Ruet, A, Borgel, F, Thouvenot, E, Moreau, T, Defer, G, Derache, N, Pelletier, J, Audoin, B, Debouverie, M, Labauge, P, Gout, O, Camu, W, Brassat, D, Brochet, B, Vermersch, P, Confavreux, C, Seze, J de

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