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Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis. [electronic resource] by
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- Tubridy, N
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- Edan, G
- Clerget-Darpoux, F
- Sémana, G
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Genes and immunity vol. 4
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122.
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Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME). [electronic resource] by
- Labauge, P
- Amer, L O
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- Tannier, C
- Clanet, M
- Castelnovo, G
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- Agid, Y
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Neurology vol. 58
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123.
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Impact of intermittent catheterization on the quality of life of multiple sclerosis patients. [electronic resource] by
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- Braley-Berthoumieux, E
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- Gasq, D
- Labrunee, M
- Viala, F
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World journal of urology vol. 31
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124.
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Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations. [electronic resource] by
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- Blecon, A
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- Arnoult, M
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Neurology vol. 72
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125.
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Guidelines for autologous blood and marrow stem cell transplantation in multiple sclerosis: a consensus report written on behalf of the European Group for Blood and Marrow Transplantation and the European Charcot Foundation. BMT-MS Study Group. [electronic resource] by
- Comi, G
- Kappos, L
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- Ebers, G
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- Fazekas, F
- Filippi, M
- Hartung, H P
- Hertenstein, B
- Karussis, D
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- van der Meché, F G
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Journal of neurology vol. 247
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126.
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Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group. [electronic resource] by
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- Mertens, C
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- Vilkoren, T
- Cournu, I
- Babron, M C
- Lyon-Caen, O
- Clerget-Darpoux, F
- Edan, G
- Clanet, M
- Brahic, M
- Bureau, J F
- Fontaine, B
- Liblau, R
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In:
Journal of neuroimmunology vol. 102
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127.
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Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations. [electronic resource] by
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- Boetto, S
- Clanet, M
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- Ibrahim, R
- Irthum, B
- Jacquet, G
- Lonjon, M
- Moreau, J J
- Neau, J P
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- Tremoulet, M
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American journal of human genetics vol. 76
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128.
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A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS. French Multiple Sclerosis Genetics Group. [electronic resource] by
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- Brassat, D
- Reboul, J
- Eichenbaum-Voline, S
- Vuillemin-Azais, C
- Cournu, I
- Babron, M C
- Semana, G
- Edan, G
- Clanet, M
- Clerget-Darpoux, F
- Baron-Van Evercooren, A
- Lyon-Caen, O
- Liblau, R
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129.
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Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility. American-French Multiple Sclerosis Genetic Group. [electronic resource] by
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- Cournu, I
- Arnaud, I
- Babron, M C
- Eichenbaum-Voline, S
- Oksenberg, J R
- Pericak-Vance, M A
- Haines, J L
- Semama, G
- Liblau, R
- Lyon-Caen, O
- Clerget-Darpoux, F
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- Hauser, S L
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In:
Genes and immunity vol. 1
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130.
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Therapeutic effect of mitoxantrone combined with methylprednisolone in multiple sclerosis: a randomised multicentre study of active disease using MRI and clinical criteria. [electronic resource] by
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- Lyon-Caen, O
- Lubetzki, C
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- Froment, J C
- Cabanis, E
- Iba-Zizen, M T
- Gandon, J M
- Lai, H M
- Moseley, I
- Sabouraud, O
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Journal of neurology, neurosurgery, and psychiatry vol. 62
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131.
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[Cerebrotendinous xanthomatosis: a multicentric retrospective study of 15 adults, clinical and paraclinical typical and atypical aspects]. [electronic resource] by
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- Ayrignac, X
- Levade, T
- Gayraud, D
- Castelnovo, G
- Besson, G
- Androdias, G
- Vukusic, S
- Confavreux, C
- Zaenker, C
- De Seze, J
- Collongues, N
- Blanc, F
- Tranchant, C
- Wallon, D
- Hannequin, D
- Gerdelat-Mas, A
- Brassat, D
- Clanet, M
- Zephir, H
- Outteryck, O
- Vermersch, P
- Labauge, P
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132.
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A second-generation genomic screen for multiple sclerosis. [electronic resource] by
- Kenealy, S J
- Babron, M-C
- Bradford, Y
- Schnetz-Boutaud, N
- Haines, J L
- Rimmler, J B
- Schmidt, S
- Pericak-Vance, M A
- Barcellos, L F
- Lincoln, R R
- Oksenberg, J R
- Hauser, S L
- Clanet, M
- Brassat, D
- Edan, G
- Yaouanq, J
- Semana, G
- Cournu-Rebeix, I
- Lyon-Caen, O
- Fontaine, B
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American journal of human genetics vol. 75
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133.
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IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. [electronic resource] by
- Weber, F
- Fontaine, B
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- Kroner, A
- Knop, M
- Lutz, S
- Müller-Sarnowski, F
- Uhr, M
- Bettecken, T
- Kohli, M
- Ripke, S
- Ising, M
- Rieckmann, P
- Brassat, D
- Semana, G
- Babron, M-C
- Mrejen, S
- Gout, C
- Lyon-Caen, O
- Yaouanq, J
- Edan, G
- Clanet, M
- Holsboer, F
- Clerget-Darpoux, F
- Müller-Myhsok, B
Producer: 20080716
In:
Genes and immunity vol. 9
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134.
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Ethics of placebo-controlled clinical trials in multiple sclerosis: a reassessment. [electronic resource] by
- Polman, C H
- Reingold, S C
- Barkhof, F
- Calabresi, P A
- Clanet, M
- Cohen, J A
- Cutter, G R
- Freedman, M S
- Kappos, L
- Lublin, F D
- McFarland, H F
- Metz, L M
- Miller, A E
- Montalban, X
- O'Connor, P W
- Panitch, H
- Richert, J R
- Petkau, J
- Schwid, S R
- Sormani, M P
- Thompson, A J
- Weinshenker, B G
- Wolinsky, J S
Producer: 20080619
In:
Neurology vol. 70
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135.
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ECTRIMS/EAN guideline on the pharmacological treatment of people with multiple sclerosis. [electronic resource] by
- Montalban, X
- Gold, R
- Thompson, A J
- Otero-Romero, S
- Amato, M P
- Chandraratna, D
- Clanet, M
- Comi, G
- Derfuss, T
- Fazekas, F
- Hartung, H P
- Havrdova, E
- Hemmer, B
- Kappos, L
- Liblau, R
- Lubetzki, C
- Marcus, E
- Miller, D H
- Olsson, T
- Pilling, S
- Selmaj, K
- Siva, A
- Sorensen, P S
- Sormani, M P
- Thalheim, C
- Wiendl, H
- Zipp, F
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In:
European journal of neurology vol. 25
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136.
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Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France? [electronic resource] by
- Frédéric, M Y
- Clot, F
- Cif, L
- Blanchard, A
- Dürr, A
- Vuillaume, I
- Lesca, G
- Kreisler, A
- Davin, C
- Besnard, T
- Rousset, F
- Thorel, D
- Saquet, C
- Mechin, D
- Ozelius, L
- Agid, Y
- Barroso, B
- Chabrol, B
- Chan, V
- Clanet, M
- Coubes, C
- Destee, A
- Nguyen, K
- Vial, C
- Vidailhet, M
- Xie, J
- Sablonniere, B
- Calender, A
- Brice, A
- Roubertie, A
- Coubes, P
- Claustres, M
- Tuffery-Giraud, S
- Collod-Beroud, G
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In:
Neurogenetics vol. 9
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137.
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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 cohort. [electronic resource] 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
- 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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In:
European journal of neurology vol. 21
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138.
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Neuromyelitis optica in France: a multicenter study of 125 patients. [electronic resource] by
- Collongues, N
- Marignier, R
- Zéphir, H
- Papeix, C
- Blanc, F
- Ritleng, C
- Tchikviladzé, M
- Outteryck, O
- Vukusic, S
- Fleury, M
- Fontaine, B
- Brassat, D
- Clanet, M
- Milh, M
- Pelletier, J
- Audoin, B
- Ruet, A
- Lebrun-Frenay, C
- Thouvenot, E
- Camu, W
- Debouverie, M
- Créange, A
- Moreau, T
- Labauge, P
- Castelnovo, G
- Edan, G
- Le Page, E
- Defer, G
- Barroso, B
- Heinzlef, O
- Gout, O
- Rodriguez, D
- Wiertlewski, S
- Laplaud, D
- Borgel, F
- Tourniaire, P
- Grimaud, J
- Brochet, B
- Vermersch, P
- Confavreux, C
- de Seze, J
Producer: 20100406
In:
Neurology vol. 74
Availability: No items available.
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