Haemorrhagic thiamine deficient encephalopathy following prolonged parenteral nutrition.

Por Vortmeyer, A O, Hagel, C, Laas, R
Publicado em 1992

Allelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas.

Por Vortmeyer, A. O., Lubensky, I. A., Fogt, F., Linehan, W. M., Khettry, U., Zhuang, Z.
Publicado em 1997

Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors.

Por Henske, E. P., Wessner, L. L., Golden, J., Scheithauer, B. W., Vortmeyer, A. O., Zhuang, Z., Klein-Szanto, A. J., Kwiatkowski, D. J., Yeung, R. S.
Publicado em 1997

Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease

Por Traoré, M., Landouré, G., Motley, W., Sangaré, M., Meilleur, K., Coulibaly, S., Traoré, S., Niaré, B., Mochel, F., La Pean, A., Vortmeyer, A., Mani, H., Fischbeck, K. H.
Publicado em 2009

Detection of human herpesvirus-6 in mesial temporal lobe epilepsy surgical brain resections

Por Donati, D., Akhyani, N., Fogdell–Hahn, A., Cermelli, C., Cassiani-Ingoni, R., Vortmeyer, A., Heiss, J. D., Cogen, P., Gaillard, W. D., Sato, S., Theodore, W. H., Jacobson, S.
Publicado no Neurology (2003)