Cervical spondylotic myelopathy and Kennedy syndrome mimicking amyotrophic lateral sclerosis

Por FISCHER, D, WULLNER, U, KLOCKGETHER, T, SCHRODER, R, WILHELM, K
Publicado em 2001

Probable multiple system atrophy in a German family

Por Wullner, U, Abele, M, Schmitz-Huebsch, T, Wilhelm, K, Benecke, R, Deuschl, G, Klockgether, T
Publicado em 2004

Dopamine transporter SPECT in patients with mitochondrial disorders

Por Minnerop, M, Kornblum, C, Joe, A, Tatsch, K, Kunz, W, Klockgether, T, Wullner, U, Reinhardt, M
Publicado em 2005

Functional implications of microbial and viral gut metagenome changes in early stage L-DOPA-naïve Parkinson’s disease patients

Por Bedarf, J. R., Hildebrand, F., Coelho, L. P., Sunagawa, S., Bahram, M., Goeser, F., Bork, P., Wüllner, U.
Publicado no Genome Med (2017)

Erratum to: Functional implications of microbial and viral gut metagenome changes in early stage L-DOPA-naïve Parkinson’s disease patients

Por Bedarf, J. R., Hildebrand, F., Coelho, L. P., Sunagawa, S., Bahram, M., Goeser, F., Bork, P., Wüllner, U.
Publicado no Genome Med (2017)

Callosal tissue loss in multiple system atrophy - a one year follow-up study

Por Minnerop, M, Luders, E, Specht, K, Ruhlmann, J, Schimke, N, Thompson, PM, Chou, YY, Toga, AW, Abele, M, Wüllner, U, Klockgether, T
Publicado em 2010

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype

Por Bauer, P, Laccone, F, Rolfs, A, Wullner, U, Bosch, S, Peters, H, Liebscher, S, Scheible, M, Epplen, J, Weber, B, Holinski-Feder, E, Weirich-Schwaiger, H, Morris-Rosendahl, D, Andrich, J, Riess, O
Publicado em 2004

The α‐synuclein gene in multiple system atrophy

Por Ozawa, T, Healy, D G, Abou‐Sleiman, P M, Ahmadi, K R, Quinn, N, Lees, A J, Shaw, K, Wullner, U, Berciano, J, Moller, J C, Kamm, C, Burk, K, Josephs, K A, Barone, P, Tolosa, E, Goldstein, D B, Wenning, G, Geser, F, Holton, J L, Gasser, T, Revesz, T, Wood, N W
Publicado em 2006