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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Auce, P, Bahlo, M, Bast, T, Becker, AJ, Becker, F, Boysen, KE, Bradfield, JP, Brody, LC, Buono, RJ, Campbell, E, Catarino, CB, Cavalleri, GL, Cherny, SS, Compston, A, Cossette, P, de Haan, G-J, de Kovel, CGF, Devinsky, O, Dlugos, DJ, Doherty, CP, Elger, CE, Eriksson, JG, Feucht, M, Francis, B, Franke, A, Gieger, C, Glauser, T, Glynn, S, Goldstein, DB, Gui, H, Haas, KF, Heinzen, EL, Helbig, I, Hengsbach, C, Hjalgrim, H, Iacomino, M, Kalviainen, R, Kantanen, A-M, Kasperaviciute, D, Trenite, DK-N, Kirsch, HE, Koeleman, BPC, Krenn, M, Kwan, P, Lau, Y-L, Lindhout, D, Lo, WD, Lopes-Cendes, I, Malovini, A, Mayer, T, McCormack, M, Mills, JL, Moerzinger, M, Moller, RS, Molloy, AM, Newton, M, Ng, P-W, Noethen, MM, O'Brien, TJ, Peter, S, Petrovski, S, Poduri, A, Privitera, M, Radtke, R, Rau, S, Reif, PS, Rosenow, F, Sander, T, Scattergood, T, Schachter, SC, Schankin, CJ, Scheffer, IE, Schmitz, B, Schoch, S, Sham, PC, Slattery, L, Smith, A, Smith, MC, Smith, PE, Speed, D, Sperling, MR, Stephani, U, Stevelink, R, Strauch, K, Striano, P, Surges, R, Tan, KM, Thomas, GN, Tozzi, R, Vining, EPG, Visscher, F, Walley, NM, Weber, YG, Weisenberg, J, Whelan, CD, Wolff, M, Wolking, S, Yang, W, Zara, F, Zimprich, F
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Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes von Heinzen, EL, Radtke, RA, Urban, TJ, Cavalleri, GL, Depondt, C, Need, AC, Walley, NM, Nicoletti, P, Ge, DL, Catarino, CB, Duncan, JS, Kasperaviciute, D, Tate, SK, Caboclo, LO, Sander, JW, Clayton, L, Linney, KN, Shianna, KV, Gumbs, CE, Smith, J, Cronin, KD, Maia, JM, Doherty, CP, Pandolfo, M, Leppert, D, Middleton, LT, Gibson, RA, Johnson, MR, Matthews, PM, Hosford, D, Kalviainen, R, Eriksson, K, Kantanen, AM, Dorn, T, Hansen, J, Kramer, G, Steinhoff, BJ, Wieser, HG, Zumsteg, D, Ortega, M, Wood, NW, Huxley-Jones, J, Mikati, M, Gallentine, WB, Husain, AM, Buckley, PG, Stallings, RL, Podgoreanu, MV, Delanty, N, Sisodiya, SM, Goldstein, DB
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Seite wird neu geladen, wenn Filter aktiviert oder ausgeschlossen wird.- 15Q13.3 Microdeletions 1 Treffer 1
- Association 1 Treffer 1
- Childhood Absence Epilepsy 1 Treffer 1
- Epilepsy 1 Treffer 1
- Febrile Seizures 1 Treffer 1
- Genes 1 Treffer 1
- Genetics Of The Nervous System 1 Treffer 1
- Genetics Research 1 Treffer 1
- Genome-Wide Association Studies 1 Treffer 1
- Idiopathic Generalized Epilepsy 1 Treffer 1
- Lateral Temporal Epilepsy 1 Treffer 1
- Mutation 1 Treffer 1
- Schizophrenia 1 Treffer 1