VPS35 Mutations in Parkinson Disease von Vilariño-Güell, Carles, Wider, Christian, Ross, Owen A., Dachsel, Justus C., Kachergus, Jennifer M., Lincoln, Sarah J., Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Wilhoite, Greggory J., Bacon, Justin A., Behrouz, Bahareh, Melrose, Heather L., Hentati, Emna, Puschmann, Andreas, Evans, Daniel M., Conibear, Elizabeth, Wasserman, Wyeth W., Aasly, Jan O., Burkhard, Pierre R., Djaldetti, Ruth, Ghika, Joseph, Hentati, Faycal, Krygowska-Wajs, Anna, Lynch, Tim, Melamed, Eldad, Rajput, Alex, Rajput, Ali H., Solida, Alessandra, Wu, Ruey-Meei, Uitti, Ryan J., Wszolek, Zbigniew K., Vingerhoets, François, Farrer, Matthew J.

Volltext

Profile of cognitive impairment and underlying pathology in multiple system atrophy von Koga, Shunsuke, Parks, Adam, Uitti, Ryan J., van Gerpen, Jay A., Cheshire, William P., Wszolek, Zbigniew K., Dickson, Dennis W.

Volltext

Validation Study of the MDS Criteria for the Diagnosis of Multiple System Atrophy in the Mayo Clinic Brain Bank von Sekiya, Hiroaki, Koga, Shunsuke, Murakami, Aya, Kawazoe, Miki, Kim, Minji, Martin, Nicholas B, Uitti, Ryan J, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W

Volltext

Genetic architecture of Parkinson’s disease subtypes – Review of the literature von Dulski, Jarosław, Uitti, Ryan J., Ross, Owen A., Wszolek, Zbigniew K.

Volltext

Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studies von Wile, Daryl J, Dr, Agarwal, Pankaj A, DM, Schulzer, Michael, Prof, Mak, Edwin, BASc, Dinelle, Katherine, MSc, Shahinfard, Elham, PhD, Vafai, Nasim, MASc, Hasegawa, Kazuko, PhD, Zhang, Jing, Prof, McKenzie, Jessamyn, LPN, Neilson, Nicole, RN, Strongosky, Audrey, BA, Uitti, Ryan J, Prof, Guttman, Mark, MD, Zabetian, Cyrus P, MD, Ding, Yu-Shin, Prof, Adam, Mike, PhD, Aasly, Jan, Prof, Wszolek, Zbigniew K, Prof, Farrer, Matthew, Prof, Sossi, Vesna, Prof, Stoessl, A Jon, Prof

Volltext

Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype von Koga, Shunsuke, Kouri, Naomi, Walton, Ronald L., Ebbert, Mark T. W., Josephs, Keith A., Litvan, Irene, Graff-Radford, Neill, Ahlskog, J. Eric, Uitti, Ryan J., van Gerpen, Jay A., Boeve, Bradley F., Parks, Adam, Ross, Owen A., Dickson, Dennis W.

Volltext

Mutations in CIZ1 cause adult onset primary cervical dystonia von Xiao, Jianfeng, Uitti, Ryan J., Zhao, Yu, Vemula, Satya R., Perlmutter, Joel S., Wszolek, Zbigniew K., Maraganore, Demetrius M., Auburger Dr Med, Georg, Leube Dr Med, Barbara, Lehnhoff, Katja, LeDoux, Mark S.

Volltext

Cancer in pathologically confirmed multiple system atrophy von Cheshire, William P., Koga, Shunsuke, Tipton, Philip W., Sekiya, Hiroaki, Ross, Owen A., Uitti, Ryan J., Josephs, Keith A., Dickson, Dennis W.

Volltext

Comparison of clinical features among Parkinson's disease subtypes: A large retrospective study in a single center von Konno, Takuya, Deutschländer, Angela, Heckman, Michael G., Ossi, Maryam, Vargas, Emily R., Strongosky, Audrey J., van Gerpen, Jay A., Uitti, Ryan J., Ross, Owen A., Wszolek, Zbigniew K.

Volltext

Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C von Koga, Shunsuke, Josephs, Keith A., Ogaki, Kotaro, Labbé, Catherine, Uitti, Ryan J., Graff-Radford, Neill, van Gerpen, Jay A., Cheshire, William P., Aoki, Naoya, Rademakers, Rosa, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W.

Volltext

Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy von Koga, Shunsuke, Sanchez‐Contreras, Monica, Josephs, Keith A., Uitti, Ryan J., Graff‐Radford, Neill, Gerpen, Jay A., Cheshire, William P., Wszolek, Zbigniew K., Rademakers, Rosa, Dickson, Dennis W.

Volltext

Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome von Kouri, Naomi, Murray, Melissa E., Hassan, Anhar, Rademakers, Rosa, Uitti, Ryan J., Boeve, Bradley F., Graff-Radford, Neill R., Wszolek, Zbigniew K., Litvan, Irene, Josephs, Keith A., Dickson, Dennis W.

Volltext

Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy von Sakae, Nobutaka, Josephs, Keith A., Litvan, Irene, Murray, Melissa E., Duara, Ranjan, Uitti, Ryan J., Wszolek, Zbigniew K., Graff‐Radford, Neil R., Dickson, Dennis W.

Volltext

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia von Rademakers, Rosa, Eriksen, Jason L., Baker, Matt, Robinson, Todd, Ahmed, Zeshan, Lincoln, Sarah J., Finch, Nicole, Rutherford, Nicola J., Crook, Richard J., Josephs, Keith A., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Parisi, Joseph E., Caselli, Richard J., Wszolek, Zbigniew K., Uitti, Ryan J., Feldman, Howard, Hutton, Michael L., Mackenzie, Ian R., Graff-Radford, Neill R., Dickson, Dennis W.

Volltext

Update on novel familial forms of Parkinson's disease and multiple system atrophy von Fujioka, Shinsuke, Ogaki, Kotaro, Tacik, Pawel M, Uitti, Ryan J, Ross, Owen A, Wszolek, Zbigniew K

Volltext

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci von Sanchez-Contreras, Monica Y, Kouri, Naomi, Cook, Casey N, Serie, Daniel J, Heckman, Michael G, Finch, NiCole A, Caselli, Richard J, Uitti, Ryan J, Wszolek, Zbigniew K, Graff-Radford, Neill, Petrucelli, Leonard, Wang, Li-San, Schellenberg, Gerard D, Dickson, Dennis W, Rademakers, Rosa, Ross, Owen A

Volltext

Latent trait modeling of tau neuropathology in progressive supranuclear palsy von Kouri, Naomi, Murray, Melissa E., Reddy, Joseph S., Serie, Daniel J., Soto-Beasley, Alexandra, Allen, Mariet, Carrasquillo, Minerva M., Wang, Xue, Castanedes, Monica Casey, Baker, Matthew C., Rademakers, Rosa, Uitti, Ryan J., Graff-Radford, Neill R., Wszolek, Zbigniew K., Schellenberg, Gerard D., Crook, Julia E., Ertekin-Taner, Nilüfer, Ross, Owen A., Dickson, Dennis W.

Volltext

Clinical features of autopsy-confirmed multiple system atrophy in the Mayo Clinic Florida brain bank von Koga, Shunsuke, Cheshire, William P., Tipton, Philip W., Driver-Dunckley, Erika D., Wszolek, Zbigniew K., Uitti, Ryan J., Graff-Radford, Neill R., van Gerpen, Jay A., Dickson, Dennis W.

Volltext

Thalamic DBS with a constant-current device in essential tremor: A controlled clinical trial von Wharen, Robert E., MD, Okun, Michael S., MD, Guthrie, Barton L., MD, Uitti, Ryan J., MD, Larson, Paul, MD, Foote, Kelly, MD, Walker, Harrison, MD, Marshall, Frederick J., MD, Schwalb, Jason, MD, Ford, Blair, MD, Jankovic, Joseph, MD, Simpson, Richard, MD, PhD, Dashtipour, Khashayar, MD, Phibbs, Fenna, MD, Neimat, Joseph S., MD, Stewart, R. Malcolm, MD, Peichel, DeLea, BS, Pahwa, Rajesh, MD, Ostrem, Jill L., MD

Volltext

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration von Kouri, Naomi, Carlomagno, Yari, Baker, Matthew, Liesinger, Amanda M., Caselli, Richard J., Wszolek, Zbigniew K., Petrucelli, Leonard, Boeve, Bradley F., Parisi, Joseph E., Josephs, Keith A., Uitti, Ryan J., Ross, Owen A., Graff-Radford, Neill R., DeTure, Michael A., Dickson, Dennis W., Rademakers, Rosa

Volltext