Suchbegriffe: MULTIPLE SCLEROSIS - GENETICS, . Treffer: 10
Sadovnick, AD; Traboulsee, AL; Bernales, CQ; Ross, JP; Forwell, AL; Yee, IM; Guillot-Noel, L; Fontaine, B; Cournu-Rebeix, I; Alcina, A; Fedetz, M; Izquierdo, G; Matesanz, F; Hilven, K; Dubois, B; Goris, A; Astobiza, I; Alloza, I; Antigüedad, A; Vandenbroeck, K; Akkad, DA; Aktas, O; Blaschke, P; Buttmann, M; Chan, A; Epplen, JT; Gerdes, LA; Kroner, A; Kubisch, C; Kümpfel, T; Lohse, P; Rieckmann, P; Zettl, UK; Zipp, F; Bertram, L; Lill, CM; Fernandez, O; Urbaneja, P; Leyva, L; Alvarez-Cermeño, JC; Arroyo, R; Garagorri, AM; García-Martínez, A; Villar, LM; Urcelay, E; Malhotra, S; Montalban, X; Comabella, M; Berger, T; Fazekas, F; Reindl, M; Schmied, MC; Zimprich, A; Vilariño-Güell, C
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
G3 (Bethesda). 2016; 6(7):2073-2079
Doi: 10.1534/g3.116.030841
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Reinthaler, E; Machetanz, G; Hotzy, C; Reindl, M; Fazekas, F; Kristoferitsch, W; Berger, T; Schmied, C; Zimprich, A
No evidence for a role of rare CYP27B1 variants in Austrian multiple sclerosis patients.
MULT SCLER J. 2014; 20(3): 391-392.
Doi: 10.1177/1352458513498130
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Williams, SK; Maier, O; Fischer, R; Fairless, R; Hochmeister, S; Stojic, A; Pick, L; Haar, D; Musiol, S; Storch, MK; Pfizenmaier, K; Diem, R
Antibody-mediated inhibition of TNFR1 attenuates disease in a mouse model of multiple sclerosis.
PLoS One. 2014; 9(2):e90117-e90117
Doi: 10.1371/journal.pone.0090117
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Schmied, MC; Zehetmayer, S; Reindl, M; Ehling, R; Bajer-Kornek, B; Leutmezer, F; Zebenholzer, K; Hotzy, C; Lichtner, P; Meitinger, T; Wichmann, HE; Illig, T; Gieger, C; Huber, K; Khalil, M; Fuchs, S; Schmidt, H; Auff, E; Kristoferitsch, W; Fazekas, F; Berger, T; Vass, K; Zimprich, A
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.
Neurogenetics. 2012; 13(2):181-187
Doi: 10.1007/s10048-012-0316-y
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Lindner, E; Weger, M; Steinwender, G; Griesbacher, A; Posch, U; Ulrich, S; Wegscheider, B; Ardjomand, N; El-Shabrawi, Y
IL2RA gene polymorphism rs2104286 A>G seen in multiple sclerosis is associated with intermediate uveitis: possible parallel pathways?
Invest Ophthalmol Vis Sci. 2011; 52(11):8295-8299
Doi: 10.1167/iovs.11-8163
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Mix, E; Ibrahim, SM; Pahnke, J; Glass, A; Mazón-Peláez, I; Lemcke, S; Koczan, D; Gimsa, U; Bansemer, S; Scheel, T; Karopka, T; Böttcher, T; Müller, J; Dazert, E; Antipova, V; Hoffrogge, R; Wree, A; Zschiesche, M; Strauss, U; Kundt, G; Warzok, R; Gierl, L; Rolfs, A
3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor Atorvastatin mediated effects depend on the activation status of target cells in PLP-EAE.
J Autoimmun. 2006; 27(4): 251-265.
Doi: 10.1016/j.jaut.2006.09.006
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Ehling, R; Gassner, Ch; Lutterotti, A; Strasser-Fuchs, S; Kollegger, H; Kristoferitsch, W; Reindl, M; Berger, T
Genetic variants in the tumor necrosis factor receptor II gene in patients with multiple sclerosis.
Tissue Antigens. 2004; 63(1):28-33
Doi: 10.1111/j.1399-0039.2004.00166.x
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Enzinger, C; Ropele, S; Smith, S; Strasser-Fuchs, S; Poltrum, B; Schmidt, H; Matthews, PM; Fazekas, F
Accelerated evolution of brain atrophy and black holes in MS patients with APOE-epsilon 4.
ANN NEUROL. 2004; 55: 563-569.
Doi: 10.1002/ana.20027
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Fazekas, F; Strasser-Fuchs, S; Kollegger, H; Berger, T; Kristoferitsch, W; Schmidt, H; Enzinger, C; Schiefermeier, M; Schwarz, C; Kornek, B; Reindl, M; Huber, K; Grass, R; Wimmer, G; Vass, K; Pfeiffer, KH; Hartung, HP; Schmidt, R
Apolipoprotein E epsilon 4 is associated with rapid progression of multiple sclerosis.
Neurology. 2001; 57(5):853-857
Doi: 10.1212/WNL.57.5.853
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Archelos, JJ; Trotter, J; Previtali, S; Weissbrich, B; Toyka, KV; Hartung, HP
Isolation and characterization of an oligodendrocyte precursor-derived B-cell epitope in multiple sclerosis.
Ann Neurol. 1998; 43(1):15-24
Doi: 10.1002/ana.410430107
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