Items where Author is "Arnold, R."
Number of items: 3. 2015Zeiser, R. and Burchert, A. and Lengerke, C. and Verbeek, M. and Maas-Bauer, K. and Metzelder, S. K. and Spoerl, S. and Ditschkowski, M. and Ecsedi, M. and Sockel, K. and Ayuk, F. and Ajib, S. and de Fontbrune, F. S. and Na, I. K. and Penter, L. and Holtick, U. and Wolf, D. and Schuler, E. and Meyer, E. and Apostolova, P. and Bertz, H. and Marks, R. and Lubbert, M. and Wasch, R. and Scheid, C. and Stolzel, F. and Ordemann, R. and Bug, G. and Kobbe, G. and Negrin, R. and Brune, M. and Spyridonidis, A. and Schmitt-Graff, A. and van der Velden, W. and Huls, G. and Mielke, S. and Grigoleit, G. U. and Kuball, J. and Flynn, R. and Ihorst, G. and Du, J. and Blazar, B. R. and Arnold, R. and Kroger, N. and Passweg, J. and Halter, J. and Socie, G. and Beelen, D. and Peschel, C. and Neubauer, A. and Finke, J. and Duyster, J. and von Bubnoff, N.. (2015) Ruxolitinib in corticosteroid-refractory graft-versus-host disease after allogeneic stem cell transplantation: a multicenter survey. Leukemia, 29 (10). pp. 2062-2068. 2008Asherson, P. and Zhou, K. and Anney, R. J. L. and Franke, B. and Buitelaar, J. and Ebstein, R. and Gill, M. and Altink, M. and Arnold, R. and Boer, F. and Brookes, K. and Buschgens, C. and Butler, L. and Cambell, D. and Chen, W. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Johansson, L. and Lubetzki, I. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Neale, B. and Rijsdijk, F. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Xu, X. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V.. (2008) A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13 (5). pp. 514-521. 2006Brookes, K. and Xu, X. and Chen, W. and Zhou, K. and Neale, B. and Lowe, N. and Anney, R. and Aneey, R. and Franke, B. and Gill, M. and Ebstein, R. and Buitelaar, J. and Sham, P. and Campbell, D. and Knight, J. and Andreou, P. and Altink, M. and Arnold, R. and Boer, F. and Buschgens, C. and Butler, L. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Korn-Lubetzki, I. and Johansson, L. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Craig, I. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Kuntsi, J. and Manor, I. and McGuffin, P. and Miranda, A. and Oades, R. D. and Plomin, R. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V. and Asherson, P.. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11 (10). pp. 934-953. |