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    Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities von Armstrong, Nicola J., Mather, Karen A., Sargurupremraj, Muralidharan, Knol, Maria J., Malik, Rainer, Satizabal, Claudia L., Yanek, Lisa R., Wen, Wei, Gudnason, Vilmundur G., Dueker, Nicole D., Elliott, Lloyd T., Hofer, Edith, Bis, Joshua, Jahanshad, Neda, Li, Shuo, Logue, Mark A., Luciano, Michelle, Scholz, Markus, Smith, Albert V., Trompet, Stella, Vojinovic, Dina, Xia, Rui, Alfaro-Almagro, Fidel, Ames, David, Amin, Najaf, Amouyel, Philippe, Beiser, Alexa S., Brodaty, Henry, Deary, Ian J., Fennema-Notestine, Christine, Gampawar, Piyush G., Gottesman, Rebecca, Griffanti, Ludovica, Jack, Clifford R., Jenkinson, Mark, Jiang, Jiyang, Kral, Brian G., Kwok, John B., Lampe, Leonie, C.M. Liewald, David, Maillard, Pauline, Marchini, Jonathan, Bastin, Mark E., Mazoyer, Bernard, Pirpamer, Lukas, Rafael Romero, José, Roshchupkin, Gennady V., Schofield, Peter R., Schroeter, Matthias L., Stott, David J., Thalamuthu, Anbupalam, Trollor, Julian, Tzourio, Christophe, van der Grond, Jeroen, Vernooij, Meike W., Witte, Veronica A., Wright, Margaret J., Yang, Qiong, Morris, Zoe, Siggurdsson, Siggi, Psaty, Bruce, Villringer, Arno, Schmidt, Helena, Haberg, Asta K., van Duijn, Cornelia M., Jukema, J. Wouter, Dichgans, Martin, Sacco, Ralph L., Wright, Clinton B., Kremen, William S., Becker, Lewis C., Thompson, Paul M., Mosley, Thomas H., Wardlaw, Joanna M., Ikram, M. Arfan, Adams, Hieab H.H., Seshadri, Sudha, Sachdev, Perminder S., Smith, Stephen M., Launer, Lenore, Longstreth, William, DeCarli, Charles, Schmidt, Reinhold, Fornage, Myriam, Debette, Stephanie, Nyquist, Paul A.

    Veröffentlicht in Stroke (1970)

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