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.

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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.

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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

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

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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology von Zimprich, Alexander, Biskup, Saskia, Leitner, Petra, Lichtner, Peter, Farrer, Matthew, Lincoln, Sarah, Kachergus, Jennifer, Hulihan, Mary, Uitti, Ryan J., Calne, Donald B., Stoessl, A.Jon, Pfeiffer, Ronald F., Patenge, Nadja, Carbajal, Iria Carballo, Vieregge, Peter, Asmus, Friedrich, Müller-Myhsok, Bertram, Dickson, Dennis W., Meitinger, Thomas, Strom, Tim M., Wszolek, Zbigniew K., Gasser, Thomas

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Rasagiline, Parkinson neuroprotection, and delayed-start trials: Still no satisfaction? von AHLSKOG, J. Eric, UITTI, Ryan J

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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

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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.

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Effects of occupational cobalt exposure on the heart in the production of cobalt and cobalt compounds: a 6-year follow-up von Linna, A., Uitti, J., Oksa, P., Toivio, P., Virtanen, V., Lindholm, H., Halkosaari, M., Sauni, R.

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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.

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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.

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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.

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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.

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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.

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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.

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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

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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.

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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.

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PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation von Adams, John R., van Netten, Hinke, Schulzer, Michael, Mak, Edwin, Mckenzie, Jessamyn, Strongosky, Audrey, Sossi, Vesna, Ruth, Thomas J., Lee, Chong S., Farrer, Matthew, Gasser, Thomas, Uitti, Ryan J., Calne, Donald B., Wszolek, Zbigniew K., Stoessl, A. Jon

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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

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