Absence of SCA1 mutation in idiopathic cerebellar ataxia.

Por Klockgether, T, Bürk, K, Schulz, J B, Dichgans, J, Wessel, K, Auburger, G
Publicado em 1994

Multiple system atrophy: natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT.

Por Schulz, J B, Klockgether, T, Petersen, D, Jauch, M, Müller-Schauenburg, W, Spieker, S, Voigt, K, Dichgans, J
Publicado em 1994

Modelling neural correlates of working memory: A coordinate-based meta-analysis

Por Rottschy, C., Langner, R., Dogan, I., Reetz, K., Laird, A.R., Schulz, J.B., Fox, P.T., Eickhoff, S.B.
Publicado em 2011

Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitrat...

Por Bruijn, L. I., Beal, M. F., Becher, M. W., Schulz, J. B., Wong, P. C., Price, D. L., Cleveland, D. W.
Publicado em 1997

Differentiated parietal connectivity of frontal regions for “what” and “where” memory

Por Rottschy, C., Caspers, S., Roski, C., Reetz, K., Dogan, I., Schulz, J. B., Zilles, K., Laird, A. R., Fox, P. T., Eickhoff, S. B.
Publicado em 2012

Rating disease progression of Friedreich’s ataxia by the International Cooperative Ataxia Rating Scale: analysis of a 603-patient database

Por Metz, Günther, Coppard, Nicholas, Cooper, Jonathon M., Delatycki, Martin B., Dürr, Alexandra, Di Prospero, Nicholas A., Giunti, Paola, Lynch, David R., Schulz, J. B., Rummey, Christian, Meier, Thomas
Publicado em 2013