Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): A single entity?

by Wider, C, Van Gerpen, J A., DeArmond, S, Shuster, E A., Dickson, D W., Wszolek, Z K.
Published 2009

Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids

by Van Gerpen, J A., Wider, C, Broderick, D F., Dickson, D W., Brown, L A., Wszolek, Z K.
Published 2008

Association of the MAPT locus with Parkinson’s disease

by Wider, C., Vilariño-Güell, C., Jasinska-Myga, B., Heckman, M. G., Soto-Ortolaza, A. I., Cobb, S. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.
Published 2009

Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1 redefining DYT14 as DYT5

by Wider, C., Melquist, S., Hauf, M., Solida, A., Cobb, S.A., Kachergus, J.M., Gass, J., Coon, K.D., Baker, M., Cannon, A., Stephan, D.A., Schorderet, D.F., Ghika, J., Burkhard, P.R., Kapatos, G., Hutton, M., Farrer, M.J., Wszolek, Z.K., Vingerhoets, F.J.G.
Published 2007

Characterization of DCTN1 genetic variability in neurodegeneration

by Vilariño-Güell, C, Wider, C, Soto-Ortolaza, A I., Cobb, S A., Kachergus, J M., Keeling, B H., Dachsel, J C., Hulihan, M M., Dickson, D W., Wszolek, Z K., Uitti, R J., Graff-Radford, N R., Boeve, B F., Josephs, K A., Miller, B, Boylan, K B., Gwinn, K, Adler, C H., Aasly, J O., Hentati, F, Destée, A, Krygowska-Wajs, A, Chartier-Harlin, M -C., Ross, O A., Rademakers, R, Farrer, M J.
Published 2009