Asymmetrical leg atrophy in Dopa Responsive Dystonia due to a novel GTP cyclohydrolase mutation

Por Mulroy, E, McCarthy, A, Costello, D, Ross, OA, Lynch, T
Publicado no Mov Disord (2014)

Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS

Por DeJesus-Hernandez, M., Desaro, P., Johnston, A., Ross, O.A., Wszolek, Z.K., Ertekin-Taner, N., Graff-Radford, N.R., Rademakers, R., Boylan, K.
Publicado em 2011

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy

Por Vilariño-Güell, C., Soto-Ortolaza, A.I., Rajput, A., Mash, D.C., Papapetropoulos, S., Pahwa, R., Lyons, K.E., Uitti, R.J., Wszolek, Z.K., Dickson, D.W., Farrer, M.J., Ross, O.A.
Publicado em 2011

A family with parkinsonism, essential tremor, restless legs syndrome, and depression

Por Puschmann, A., Pfeiffer, R.F., Stoessl, A.J., Kuriakose, R., Lash, J.L., Searcy, J.A., Strongosky, A.J., Vilariño-Güell, C., Farrer, M.J., Ross, O.A., Dickson, D.W., Wszolek, Z.K.
Publicado em 2011

AN INDEPENDENT REPLICATION OF PARK16 IN ASIAN SAMPLES

Por Vilariño-Güell, C., Ross, O.A., Aasly, J.O., White, L.R., Rajput, A., Rajput, A.H., Lynch, T., Krygowska-Wajs, A., Jasinska-Myga, B., Opala, G., Barcikowska, M., Lee, M.-C., Hentati, F., Uitti, R.J., Wszolek, Z.K., Farrer, M.J., Wu, R.-M.
Publicado em 2010

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Por Haugarvoll, K., Rademakers, R., Kachergus, J.M., Nuytemans, K., Ross, O.A., Gibson, J.M., Tan, E.-K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P., De Deyn, P. Paul, Engelborghs, S., Pickut, B., Uitti, R.J., Foroud, T., Nichols, W.C., Hagenah, J., Klein, C., Samii, A., Zabetian, C.P., Bonifati, V., Van Broeckhoven, C., Farrer, M.J., Wszolek, Z.K.
Publicado em 2008