Endovascular treatment of genetically linked aortic diseases

Por Böckler, D., Meisenbacher, K., Peters, A. S., Grond-Ginsbach, C., Bischoff, M. S.
Publicado no Gefasschirurgie (2017)

MTHFR 677TT genotype increases the risk for cervical artery dissections

Por Kloss, M, Wiest, T, Hyrenbach, S, Werner, I, Arnold, M‐L, Lichy, C, Grond‐Ginsbach, C
Publicado em 2006

A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors.

Por Brune, W., Weber, R. G., Saul, B., von Knebel Doeberitz, M., Grond-Ginsbach, C., Kellerman, K., Meinck, H. M., Becker, C. M.
Publicado em 1996