Works by Uitti, Ryan J.

Results: 87

A Consensus Set of Outcomes for Parkinson's Disease from the International Consortium for Health Outcomes Measurement.

Published in:

Journal of Parkinson's Disease, 2017, v. 7, n. 3, p. 533, doi. 10.3233/JPD-161055

By:

de Roos, Paul;
Bloem, Bastiaan R.;
Kelley, Thomas A.;
Antonini, Angelo;
Dodel, Richard;
Hagell, Peter;
Marras, Connie;
Martinez-Martin, Pablo;
Mehta, Shyamal H.;
Odin, Per;
Chaudhuri, Kallol Ray;
Weintraub, Daniel;
Wilson, Bil;
Uitti, Ryan J.

Publication type:

Article

Occupational histories in neuropathologically confirmed multiple system atrophy.

Published in:

Clinical Autonomic Research, 2025, v. 35, n. 3, p. 421, doi. 10.1007/s10286-025-01109-9

By:

Cheshire, William P.;
Tipton, Philip W.;
Koga, Shunsuke;
Sekiya, Hiroaki;
Uitti, Ryan J.;
Ross, Owen A.;
Heckman, Michael G.;
Sledge, Hanna J.;
Dickson, Dennis W.

Publication type:

Article

Association of MAPT subhaplotypes with clinical and demographic features in Parkinson's disease.

Published in:

Annals of Clinical & Translational Neurology, 2020, v. 7, n. 9, p. 1557, doi. 10.1002/acn3.51139

By:

Deutschlander, Angela B.;
Konno, Takuya;
Soto‐Beasley, Alexandra I.;
Walton, Ronald L.;
Gerpen, Jay A.;
Uitti, Ryan J.;
Heckman, Michael G.;
Wszolek, Zbigniew K.;
Ross, Owen A.

Publication type:

Article

Cancer in pathologically confirmed multiple system atrophy.

Published in:

Clinical Autonomic Research, 2023, v. 33, n. 4, p. 451, doi. 10.1007/s10286-023-00946-w

By:

Cheshire, William P.;
Koga, Shunsuke;
Tipton, Philip W.;
Sekiya, Hiroaki;
Ross, Owen A.;
Uitti, Ryan J.;
Josephs, Keith A.;
Dickson, Dennis W.

Publication type:

Article

Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy.

Published in:

Clinical Autonomic Research, 2021, v. 31, n. 1, p. 117, doi. 10.1007/s10286-020-00759-1

By:

Wernick, Anna I.;
Walton, Ronald L.;
Soto-Beasley, Alexandra I.;
Koga, Shunsuke;
Heckman, Michael G.;
Valentino, Rebecca R.;
Milanowski, Lukasz M.;
Hoffman-Zacharska, Dorota;
Koziorowski, Dariusz;
Hassan, Anhar;
Uitti, Ryan J.;
Cheshire, William P.;
Singer, Wolfgang;
Wszolek, Zbigniew K.;
Dickson, Dennis W.;
Low, Phillip A.;
Ross, Owen A.

Publication type:

Article

Neurological Disorders and Services in Saskatchewan - A Report Based on Provincial Health Care Records.

Published in:

Neuroepidemiology, 1988, v. 7, n. 3, p. 145, doi. 10.1159/000110148

By:

Rajput, A.H.;
Uitti, Ryan J.;
Rajput, Alex H.

Publication type:

Article

Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau Pathology.

Published in:

JAMA Neurology, 2019, v. 76, n. 6, p. 710, doi. 10.1001/jamaneurol.2019.0250

By:

Heckman, Michael G.;
Brennan, Rebecca R.;
Labbé, Catherine;
Soto, Alexandra I.;
Koga, Shunsuke;
DeTure, Michael A.;
Murray, Melissa E.;
Petersen, Ronald C.;
Boeve, Bradley F.;
van Gerpen, Jay A.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Rademakers, Rosa;
Dickson, Dennis W.;
Ross, Owen A.

Publication type:

Article

Fine-mapping and candidate gene investigation within the PARK10 locus.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 3, p. 336, doi. 10.1038/ejhg.2008.187

By:

Haugarvoll, Kristoffer;
Toft, Mathias;
Skipper, Lisa;
Heckman, Michael G.;
Crook, Julia E.;
Soto, Alexandra;
Ross, Owen A.;
Hulihan, Mary M.;
Kachergus, Jennifer M.;
Sando, Sigrid B.;
White, Linda R.;
Lynch, Timothy;
Gibson, J. Mark;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Aasly, Jan O.;
Farrer, Matthew J.

Publication type:

Article

Underlying pathology identified after 20 years of disease course in two cases of slowly progressive frontotemporal dementia syndromes.

Published in:

2021

By:

Hokelekli, Fatma Ozlem;
Whitwell, Jennifer L.;
Machulda, Mary M.;
Jones, David T.;
Uitti, Ryan J.;
Pham, Nha Trang Thu;
Giannini, Caterina;
Baker, Matthew;
Lowe, Val J.;
Dickson, Dennis W.;
Josephs, Keith A.

Publication type:

journal article

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

Published in:

Nature Genetics, 2011, v. 43, n. 7, p. 699, doi. 10.1038/ng.859

By:

Höglinger, Günter U.;
Melhem, Nadine M.;
Dickson, Dennis W.;
Sleiman, Patrick M. A.;
Li-San Wang;
Klei, Lambertus;
Rademakers, Rosa;
de Silva, Rohan;
Litvan, Irene;
Riley, David E.;
van Swieten, John C.;
Heutink, Peter;
Wszolek, Zbigniew K.;
Uitti, Ryan J.;
Vandrovcova, Jana;
Hurtig, Howard I.;
Gross, Rachel G.;
Maetzler, Walter;
Goldwurm, Stefano;
Tolosa, Eduardo

Publication type:

Article

Gender and the Parkinson’s disease phenotype.

Published in:

Journal of Neurology, 2005, v. 252, n. 10, p. 1201, doi. 10.1007/s00415-005-0835-7

By:

Baba, Yasuhiko;
Putzke, John D.;
Whaley, Nathaniel R.;
Wszolek, Zbigniew K.;
Uitti, Ryan J.

Publication type:

Article

Cognitive impairment in progressive supranuclear palsy is associated with tau burden.

Published in:

Movement Disorders, 2017, v. 32, n. 12, p. 1772, doi. 10.1002/mds.27198

By:

Koga, Shunsuke;
Parks, Adam;
Kasanuki, Koji;
Sanchez‐Contreras, Monica;
Baker, Matthew C.;
Josephs, Keith A.;
Ahlskog, J. Eric;
Uitti, Ryan J.;
Graff‐Radford, Neill;
van Gerpen, Jay A.;
Wszolek, Zbigniew K.;
Rademakers, Rosa;
Dickson, Dennis W.

Publication type:

Article

Profile of cognitive impairment and underlying pathology in multiple system atrophy.

Published in:

2017

By:

Koga, Shunsuke;
Parks, Adam;
Uitti, Ryan J.;
van Gerpen, Jay A.;
Cheshire, William P.;
Wszolek, Zbigniew K.;
Dickson, Dennis W.

Publication type:

journal article

Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy.

Published in:

2017

By:

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.;
Sanchez-Contreras, Monica;
Graff-Radford, Neill;
van Gerpen, Jay A

Publication type:

journal article

Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.

Published in:

2016

By:

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.

Publication type:

journal article

Cognitive profile of LRRK2-related Parkinson's disease.

Published in:

Movement Disorders, 2015, v. 30, n. 5, p. 728, doi. 10.1002/mds.26161

By:

Srivatsal, Sindhu;
Cholerton, Brenna;
Leverenz, James B.;
Wszolek, Zbigniew K.;
Uitti, Ryan J.;
Dickson, Dennis W.;
Weintraub, Daniel;
Trojanowski, John Q.;
Van Deerlin, Vivianna M.;
Quinn, Joseph F.;
Chung, Kathryn A.;
Peterson, Amie L.;
Factor, Stewart A.;
Wood‐Siverio, Cathy;
Goldman, Jennifer G.;
Stebbins, Glenn T.;
Bernard, Bryan;
Ritz, Beate;
Rausch, Rebecca;
Espay, Alberto J.

Publication type:

Article

Genetic variants of α-synuclein are not associated with essential tremor.

Published in:

2011

By:

Ross OA;
Conneely KN;
Wang T;
Vilarino-Guell C;
Soto-Ortolaza AI;
Rajput A;
Wszolek ZK;
Uitti RJ;
Louis ED;
Clark LN;
Farrer MJ;
Testa CM;
Ross, Owen A;
Conneely, Karen N;
Wang, Tao;
Vilarino-Guell, Carles;
Soto-Ortolaza, Alexandra I;
Rajput, Alex;
Wszolek, Zbigniew K;
Uitti, Ryan J

Publication type:

journal article

Genetic variants of α-synuclein are not associated with essential tremor.

Published in:

Movement Disorders, 2011, v. 26, n. 14, p. 2552, doi. 10.1002/mds.23909

By:

Ross, Owen A.;
Conneely, Karen N.;
Wang, Tao;
Vilarino-Guell, Carles;
Soto-Ortolaza, Alexandra I.;
Rajput, Alex;
Wszolek, Zbigniew K.;
Uitti, Ryan J.;
Louis, Elan D.;
Clark, Lorraine N.;
Farrer, Matthew J.;
Testa, Claudia M.

Publication type:

Article

The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia.

Published in:

Movement Disorders, 2011, v. 26, n. 3, p. 549, doi. 10.1002/mds.23551

By:

Xiao, Jianfeng;
Zhao, Yu;
Bastian, Robert W.;
Perlmutter, Joel S.;
Racette, Brad A.;
Tabbal, Samer D.;
Karimi, Morvarid;
Paniello, Randal C.;
Wszolek, Zbigniew K.;
Uitti, Ryan J.;
Van Gerpen, Jay A.;
Simon, David K.;
Tarsy, Daniel;
Hedera, Peter;
Truong, Daniel D.;
Frei, Karen P.;
Blitzer, Andrew;
Rudzińska, Monika;
Pfeiffer, Ronald F.;
Le, Carrie

Publication type:

Article

Mortality in Parkinson's disease.

Published in:

Movement Disorders, 2010, v. 25, n. 4, p. 507, doi. 10.1002/mds.22914

By:

Rajput, Ali H.;
Uitti, Ryan J.;
Rajput, Alex;
Offord, Kenneth P.

Publication type:

Article

GCH1 in early-onset Parkinson's disease.

Published in:

Movement Disorders, 2009, v. 24, n. 14, p. 2070, doi. 10.1002/mds.22729

By:

Cobb, Stephanie A.;
Wider, Christian;
Ross, Owen A.;
Mata, Ignacio F.;
Adler, Charles H.;
Rajput, Alex;
Rajput, Ali H.;
Wu, Ruey-Meei;
Hauser, Robert;
Josephs, Keith A.;
Carr, Jonathan;
Gwinn, Katrina;
Heckman, Michael G.;
Aasly, Jan O.;
Lynch, Timothy;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Kapatos, Gregory;
Farrer, Matthew J.

Publication type:

Article

Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.

Published in:

Movement Disorders, 2009, v. 24, n. 4, p. 619, doi. 10.1002/mds.22451

By:

Vilariño-Güell, Carles;
Ross, Owen A.;
Soto, Alexandra I.;
Farrer, Matthew J.;
Haugarvoll, Kristoffer;
Aasly, Jan O.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.

Publication type:

Article

FGF20 and Parkinson's disease: No evidence of association or pathogenicity via α-synuclein expression.

Published in:

Movement Disorders, 2009, v. 24, n. 3, p. 455, doi. 10.1002/mds.22442

By:

Wider, Christian;
Dachsel, Justus C.;
Soto, Alexandra I.;
Heckman, Michael G.;
Diehl, Nancy N.;
Yue, Mei;
Lincoln, Sarah;
Aasly, Jan O.;
Haugarvoll, Kristoffer;
Trojanowski, John Q.;
Papapetropoulos, Spiridon;
Mash, Deborah;
Rajput, Alex;
Rajput, Ali H.;
Gibson, J. Mark;
Lynch, Timothy;
Dickson, Dennis W.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Farrer, Matthew J.

Publication type:

Article

Progranulin gene mutation with an unusual clinical and neuropathologic presentation.

Published in:

Movement Disorders, 2008, v. 23, n. 8, p. 1168, doi. 10.1002/mds.22065

By:

Wider, Christian;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Fang, John Y.;
Josephs, Keith A.;
Baker, Matthew C.;
Rademakers, Rosa;
Hutton, Michael L.;
Dickson, Dennis W.

Publication type:

Article

ELAVL4, PARK10, and the Celts.

Published in:

2007

By:

Haugarvoll, Kristoffer;
Toft, Mathias;
Ross, Owen A.;
Stone, Jeremy T.;
Heckman, Michael G.;
White, Linda R.;
Lynch, Timothy;
Gibson, John Mark;
Wszolek, Zbigniew K.;
Uitti, Ryan J.;
Aasly, Jan O.;
Farrer, Matthew J.

Publication type:

journal article

Progressive supranuclear palsy: Phenotypic sex differences in a clinical cohort.

Published in:

Movement Disorders, 2006, v. 21, n. 5, p. 689, doi. 10.1002/mds.20769

By:

Baba, Yasuhiko;
Putzke, John D.;
Whaley, Nathaniel R.;
Wszolek, Zbigniew K.;
Uitti, Ryan J.

Publication type:

Article

Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome.

Published in:

Movement Disorders, 2005, v. 20, n. 8, p. 982, doi. 10.1002/mds.20478

By:

Tsuboi, Yoshio;
Josephs, Keith A.;
Boeve, Bradley F.;
Litvan, Irene;
Caselli, Richard J.;
Caviness, John N.;
Uitti, Ryan J.;
Bott, Allen D.;
Dickson, Dennis W.

Publication type:

Article

Parkinsonism, FXTAS, and FMR1 premutations.

Published in:

Movement Disorders, 2005, v. 20, n. 2, p. 230, doi. 10.1002/mds.20297

By:

Toft, Mathias;
Aasly, Jan;
Bisceglio, Gina;
Adler, Charles H.;
Uitti, Ryan J.;
Krygowska-Wajs, Anna;
Lynch, Timothy;
Wszolek, Zbigniew K.;
Farrer, Matthew J.

Publication type:

Article

The effect of dopamine agonist therapy on dopamine transporter imaging in Parkinson's disease.

Published in:

Movement Disorders, 1999, v. 14, n. 6, p. 940, doi. 10.1002/1531-8257(199911)14:6<940::AID-MDS1005>3.0.CO;2-Y

By:

Ahlskog, J. Eric;
Uitti, Ryan J.;
O'Connor, Michael K.;
Maraganore, Demetrius M.;
Matsumoto, Joseph Y.;
Stark, Kathy F.;
Turk, Margaret F.;
Burnett, Omer L.

Publication type:

Article

Letters to the Editor.

Published in:

Movement Disorders, 1998, v. 13, n. 5, p. 851, doi. 10.1002/mds.870130520

By:

Rajput, Ali H.;
Rajput, Alex;
Lang, Anthony E.;
Kumar, Rajeev;
Uitti, Ryan J.;
Le Couteur, David G.;
McCann, Sally J.;
Becher, Mark W.;
Ross, Christopher A.;
Hardie, Richard

Publication type:

Article

Letters to the editor.

Published in:

Movement Disorders, 1996, v. 11, n. 3, p. 342, doi. 10.1002/mds.870110327

By:

Louis, Elan D.;
Nakashima, Kenji;
Kusumi, Masayoshi;
Takahashi, Kazuro;
Inoue, Yuichi;
Uitti, Ryan J.;
Ahlskog, J. Eric;
Maraganore, D. M.;
Lang, Anthony E.

Publication type:

Article

No evidence for systemic oxidant stress in Parkinson's or Alzheimer's disease.

Published in:

Movement Disorders, 1995, v. 10, n. 5, p. 566, doi. 10.1002/mds.870100507

By:

Ahlskog, J. Eric;
Uitti, Ryan J.;
Low, Phillip A.;
Tyce, Gertrude M.;
Nickander, Kim K.;
Petersen, Ronald C.;
Kokmen, Emre

Publication type:

Article

Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred.

Published in:

Acta Neuropathologica, 2006, v. 111, n. 4, p. 300, doi. 10.1007/s00401-006-0046-z

By:

Baba, Yasuhiko;
Ghetti, Bernardino;
Baker, Matthew C.;
Uitti, Ryan J.;
Hutton, Michael L.;
Yamaguchi, Keiji;
Bird, Thomas;
Wenlang Lin;
DeLucia, Michael W.;
Dickson, Dennis W.;
Wszolek, Zbigniew K.

Publication type:

Article

Diagnostic utility of 7T neuromelanin imaging of the substantia nigra in Parkinson's disease.

Published in:

NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00631-3

By:

Lakhani, Dhairya A.;
Zhou, Xiangzhi;
Tao, Shengzhen;
Patel, Vishal;
Wen, Sijin;
Okromelidze, Lela;
Greco, Elena;
Lin, Chen;
Westerhold, Erin M.;
Straub, Sina;
Wszolek, Zbigniew K.;
Tipton, Philip W.;
Uitti, Ryan J.;
Grewal, Sanjeet S.;
Middlebrooks, Erik H.

Publication type:

Article

Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures.

Published in:

Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01399-4

By:

Valentino, Rebecca R.;
Ramnarine, Chloe;
Heckman, Michael G.;
Johnson, Patrick W.;
Soto-Beasley, Alexandra I.;
Walton, Ronald L.;
Koga, Shunsuke;
Kasanuki, Koji;
Murray, Melissa E.;
Uitti, Ryan J.;
Fields, Julie A.;
Botha, Hugo;
Ramanan, Vijay K.;
Kantarci, Kejal;
Lowe, Val J.;
Jack, Clifford R.;
Ertekin-Taner, Nilufer;
Savica, Rodolfo;
Graff-Radford, Jonathan;
Petersen, Ronald C.

Publication type:

Article

MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features.

Published in:

Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-01097-z

By:

Valentino, Rebecca R.;
Koga, Shunsuke;
Walton, Ronald L.;
Soto-Beasley, Alexandra I.;
Kouri, Naomi;
DeTure, Michael A.;
Murray, Melissa E.;
Johnson, Patrick W.;
Petersen, Ronald C.;
Boeve, Bradley F.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Dickson, Dennis W.;
Ross, Owen A.;
Heckman, Michael G.

Publication type:

Article

Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy.

Published in:

Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01050-0

By:

Strickland, Samantha L.;
Morel, Hélène;
Prusinski, Christian;
Allen, Mariet;
Patel, Tulsi A.;
Carrasquillo, Minerva M.;
Conway, Olivia J.;
Lincoln, Sarah J.;
Reddy, Joseph S.;
Nguyen, Thuy;
Malphrus, Kimberly G.;
Soto, Alexandra I.;
Walton, Ronald L.;
Crook, Julia E.;
Murray, Melissa E.;
Boeve, Bradley F.;
Petersen, Ronald C.;
Lucas, John A.;
Ferman, Tanis J.;
Uitti, Ryan J.

Publication type:

Article

Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures.

Published in:

Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01035-z

By:

Valentino, Rebecca R.;
Tamvaka, Nikoleta;
Heckman, Michael G.;
Johnson, Patrick W.;
Soto-Beasley, Alexandra I.;
Walton, Ronald L.;
Koga, Shunsuke;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Dickson, Dennis W.;
Ross, Owen A.

Publication type:

Article

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson’s Disease Locus.

Published in:

PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128586

By:

Labbé, Catherine;
Ogaki, Kotaro;
Lorenzo-Betancor, Oswaldo;
Carrasquillo, Minerva M.;
Heckman, Michael G.;
McCarthy, Allan;
Soto-Ortolaza, Alexandra I.;
Walton, Ronald L.;
Lynch, Timothy;
Siuda, Joanna;
Opala, Grzegorz;
Krygowska-Wajs, Anna;
Barcikowska, Maria;
Czyzewski, Krzysztof;
Dickson, Dennis W.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Ross, Owen A.

Publication type:

Article

Analysis of Nuclear Export Sequence Regions of FUS-Related RNA-Binding Proteins in Essential Tremor.

Published in:

PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111989

By:

Lorenzo-Betancor, Oswaldo;
Ogaki, Kotaro;
Soto-Ortolaza, Alexandra;
Labbé, Catherine;
Vilariño-Güell, Carles;
Rajput, Alex;
Rajput, Ali H.;
Pastor, Pau;
Ortega, Sara;
Lorenzo, Elena;
Strongosky, Audrey J.;
van Gerpen, Jay A.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Ross, Owen A.

Publication type:

Article

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research.

Published in:

PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043099

By:

Wray, Selina;
Self, Matthew;
Lewis, Patrick A.;
Taanman, Jan-Willem;
Ryan, Natalie S.;
Mahoney, Colin J.;
Yuying Liang;
Devine, Michael J.;
Sheerin, Una-Marie;
Houlden, Henry;
Morris, Huw R.;
Healy, Daniel;
Marti-Masso, Jose-Felix;
Preza, Elisavet;
Barker, Suzanne;
Sutherland, Margaret;
Corriveau, Roderick A.;
D'Andrea, Michael;
Schapira, Anthony H. V.;
Uitti, Ryan J.

Publication type:

Article

Evaluation of the Role of SNCA Variants in Survival without Neurological Disease.

Published in:

PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0042877

By:

Heckman, Michael G.;
Soto-Ortolaza, Alexandra I.;
Diehl, Nancy N.;
Carrasquillo, Minerva M.;
Uitti, Ryan J.;
Wszolek, Zbigniew K.;
Graff-Radford, Neill R.;
Ross, Owen A.;
Toft, Mathias

Publication type:

Article

Parkinsonism and neurofibrillary tangle pathology in pigmented nuclei.

Published in:

Annals of Neurology, 1989, v. 25, n. 6, p. 602, doi. 10.1002/ana.410250612

By:

Rajput, A. H.;
Uitti, Ryan J.;
Sudhakar, S.;
Rozdilsky, B.

Publication type:

Article

Frontotemporal dementia and parkinsonism linked to chromosome 17 with the N279K tau mutation.

Published in:

Neuropathology, 2007, v. 27, n. 1, p. 73, doi. 10.1111/j.1440-1789.2006.00742.x

By:

Slowinski, Jerzy;
Dominik, Jake;
Uitti, Ryan J.;
Ahmed, Zeshan;
Dickson, Dennis D.;
Wszolek, Zbigniew K.

Publication type:

Article

PTPA variants are rare in early-onset and familial Parkinson's disease.

Published in:

Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. e125, doi. 10.1093/brain/awad244

By:

Dulski, Jarosław;
Soto-Beasley, Alexandra I;
Uitti, Ryan J;
Wszolek, Zbigniew K;
Ross, Owen A

Publication type:

Article

Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome.

Published in:

Brain: A Journal of Neurology, 2011, v. 134, n. 11, p. 3264, doi. 10.1093/brain/awr234

By:

Kouri, Naomi;
Murray, Melissa E.;
Hassan, Anhar;
Rademakers, Rosa;
Uitti, Ryan J.;
Boeve, Bradley F.;
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PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation.

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Chong S. Lee;
Matthew Farrer;
Thomas Gasser;
Ryan J. Uitti;
Donald B. Calne;
Zbigniew K. Wszolek;
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Tipton, Philip W.;
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Characterizing the cognitive phenotype of Parkinson's disease: Neuropsychiatry and behavioral neurology/Behavioral neurology.

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Tipton, Philip W.;
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Clinicopathologic subtype of Alzheimer's disease presenting as corticobasal syndrome.

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Sakae, Nobutaka;
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