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Autosomal dominant SPG9: intrafamilial variability and onset during pregnancy.
Published in:
Neurological Sciences, 2020, v. 41, n. 7, p. 1931, doi. 10.1007/s10072-020-04341-5
By:
- Marelli, C.;
- Badiou, S.;
- Genestet, S.;
- Larrieu, L.;
- Damier, P.;
- Camu, W.;
- Planes, M.;
- Koenig, M.;
- Guissart, C.
Publication type:
Article
FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.
Published in:
2010
By:
- Broustal O;
- Camuzat A;
- Guillot-Noël L;
- Guy N;
- Millecamps S;
- Deffond D;
- Lacomblez L;
- Golfier V;
- Hannequin D;
- Salachas F;
- Camu W;
- Didic M;
- Dubois B;
- Meininger V;
- Le Ber I;
- Brice A;
- French clinical and genetic research network on FTD/FTD-MND
Publication type:
Journal Article
SOD1 mutation can mask C9 orf72 abnormal expansion.
Published in:
European Journal of Neurology, 2017, v. 24, n. 4, p. e24, doi. 10.1111/ene.13257
By:
- Corcia, P.;
- Blasco, H.;
- Besson, G.;
- Camdessanché, J. ‐ P.;
- Pautot, V.;
- Beltran, S.;
- Couratier, P.;
- Andres, C.;
- Camu, W.;
- Vourc'h, P.
Publication type:
Article
Vitamin D is associated with degree of disability in patients with fully ambulatory relapsing-remitting multiple sclerosis.
Published in:
European Journal of Neurology, 2015, v. 22, n. 3, p. 564, doi. 10.1111/ene.12617
By:
- Thouvenot, E.;
- Orsini, M.;
- Daures, J. ‐ P.;
- Camu, W.
Publication type:
Article
A prospective observational post-marketing study of natalizumab-treated multiple sclerosis patients: clinical, radiological and biological features and adverse events. The BIONAT cohort.
Published in:
European Journal of Neurology, 2014, v. 21, n. 1, p. 40, doi. 10.1111/ene.12204
By:
- 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.
Publication type:
Article
APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in men.
Published in:
European Journal of Neurology, 2011, v. 18, n. 8, p. 1046, doi. 10.1111/j.1468-1331.2010.03330.x
By:
- Praline, J.;
- Blasco, H.;
- Vourc'h, P.;
- Garrigue, M.-A.;
- Gordon, P. H.;
- Camu, W.;
- Corcia, P.;
- Andres, C. R.
Publication type:
Article
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study.
Published in:
European Journal of Neurology, 2008, v. 15, n. 11, p. 1245, doi. 10.1111/j.1468-1331.2008.02307.x
By:
- 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.
Publication type:
Article
Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country.
Published in:
European Journal of Neurology, 2000, v. 7, n. 2, p. 207, doi. 10.1046/j.1468-1331.2000.00028.x
By:
- Khoris, J.;
- Moulard, B.;
- Briolotti, V.;
- Hayer, M.;
- Durieux, A.;
- Clavelou, P.;
- Malafosse, A.;
- Rouleau, G. A.;
- Camu, W.
Publication type:
Article
Erythema nodosum and glatiramer acetate treatment in relapsing-remitting multiple sclerosis.
Published in:
Multiple Sclerosis (13524585), 2007, v. 13, n. 7, p. 941, doi. 10.1177/1352458507076385
By:
- Thouvenot, E.;
- Hillaire-Buys, D.;
- Bos-Thompson, M. A.;
- Rigau, V.;
- Durand, L.;
- Guillot, B.;
- Camu, W.
Publication type:
Article
Chitinase 3-like proteins as diagnostic and prognostic biomarkers of multiple sclerosis.
Published in:
Multiple Sclerosis Journal, 2015, v. 21, n. 10, p. 1251, doi. 10.1177/1352458514561906
By:
- 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.
Publication type:
Article
High-risk syndrome for neuromyelitis optica: a descriptive and comparative study.
Published in:
Multiple Sclerosis Journal, 2011, v. 17, n. 6, p. 720, doi. 10.1177/1352458510396923
By:
- 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.
Publication type:
Article
Cutaneous adverse events related to glatiramer acetate injection (copolymer-1, Copaxone<sup> ®</sup>).
Published in:
2009
By:
- Kluger, N.;
- Thouvenot, E.;
- Camu, W.;
- Guillot, B.
Publication type:
Letter
Fasting plasma and CSF amino acid levels in amyotrophic lateral sclerosis: a subtype analysis.
Published in:
Acta Neurologica Scandinavica, 1993, v. 88, n. 1, p. 51, doi. 10.1111/j.1600-0404.1993.tb04186.x
By:
- Camu, W.;
- Billiard, M.;
- Baldy-Moulinier, M.
Publication type:
Article
Serum neurofilament light chain at time of diagnosis is an independent prognostic factor of survival in amyotrophic lateral sclerosis.
Published in:
European Journal of Neurology, 2020, v. 27, n. 2, p. 251, doi. 10.1111/ene.14063
By:
- Thouvenot, E.;
- Demattei, C.;
- Lehmann, S.;
- Maceski‐Maleska, A.;
- Hirtz, C.;
- Juntas‐Morales, R.;
- Pageot, N.;
- Esselin, F.;
- Alphandéry, S.;
- Vincent, T.;
- Camu, W.
Publication type:
Article
Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.
Published in:
2001
By:
- Hand, Collette K.;
- Mayeux-Portas, Veronique;
- Khoris, Jawad;
- Briolotti, Valerie;
- Clavelou, Pierre;
- Camu, William;
- Rouleau, Guy A.;
- Hand, C K;
- Mayeux-Portas, V;
- Khoris, J;
- Briolotti, V;
- Clavelou, P;
- Camu, W;
- Rouleau, G A
Publication type:
journal article

Found: 15