Works matching AU Wszolek, Zbigniew K.

Results: 229

A 43-year-old female with personality changes and alien limb.

Published in:

Oxford Medical Case Reports, 2025, v. 2025, n. 5, p. 1, doi. 10.1093/omcr/omaf038

By:

Zahid, Anza;
Wszolek, Zbigniew K;
Alchaki, Abdul R

Publication type:

Article

Evaluating Glial Fibrillary Acidic Protein and Neurofilament Light as Potential Biomarkers for Spinocerebellar Ataxia 7.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 11, p. 5070, doi. 10.3390/ijms26115070

By:

Hanna Al-Shaikh, Rana;
Jansen-West, Karen;
Strongosky, Audrey;
Parrales, Zoe;
Dunmore, Judith A.;
Song, Yuping;
Gendron, Tania F.;
Guevara, Juan C.;
Teive, Helio A. G.;
Dulski, Jarosław;
Sławek, Jarosław;
Petrucelli, Leonard;
Wszolek, Zbigniew K.;
Prudencio, Mercedes

Publication type:

Article

Genetic Screening and Functional Characterization of PDGFRB Mutations Associated with Basal Ganglia Calcification of Unknown Etiology.

Published in:

Human Mutation, 2014, v. 35, n. 8, p. 964, doi. 10.1002/humu.22582

By:

Sanchez‐Contreras, Monica;
Baker, Matthew C.;
Finch, NiCole A.;
Nicholson, Alexandra;
Wojtas, Aleksandra;
Wszolek, Zbigniew K.;
Ross, Owen A.;
Dickson, Dennis W.;
Rademakers, Rosa

Publication type:

Article

Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death.

Published in:

Human Mutation, 2011, v. 32, n. 12, p. 1390, doi. 10.1002/humu.21582

By:

Angeles, Dario C.;
Gan, Bong-Hwa;
Onstead, Luisa;
Zhao, Yi;
Lim, Kah-Leong;
Dachsel, Justus;
Melrose, Heather;
Farrer, Matt;
Wszolek, Zbigniew K.;
Dickson, Dennis W.;
Tan, Eng-King

Publication type:

Article

De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.

Published in:

Human Mutation, 2010, v. 31, n. 5, p. E1377, doi. 10.1002/humu.21241

By:

DeJesus-Hernandez, Mariely;
Kocerha, Jannet;
Finch, NiCole;
Crook, Richard;
Baker, Matt;
Desaro, Pamela;
Johnston, Amelia;
Rutherford, Nicola;
Wojtas, Aleksandra;
Kennelly, Kathleen;
Wszolek, Zbigniew K.;
Graff-Radford, Neill;
Boylan, Kevin;
Rademakers, Rosa

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

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

Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.

Published in:

JAMA Neurology, 2022, v. 79, n. 2, p. 185, doi. 10.1001/jamaneurol.2021.4781

By:

Liao, Calwing;
Castonguay, Charles-Etienne;
Heilbron, Karl;
Vuokila, Veikko;
Medeiros, Miranda;
Houle, Gabrielle;
Akçimen, Fulya;
Ross, Jay P.;
Catoire, Helene;
Diez-Fairen, Monica;
Kang, Jooeun;
Mueller, Stefanie H.;
Girard, Simon L.;
Hopfner, Franziska;
Lorenz, Delia;
Clark, Lorraine N.;
Soto-Beasley, Alexandra I.;
Klebe, Stephan;
Hallett, Mark;
Wszolek, Zbigniew K.

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

Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.

Published in:

JAMA Neurology, 2016, v. 73, n. 10, p. 1217, doi. 10.1001/jamaneurol.2016.2245

By:

Davis, Marie Y.;
Johnson, Catherine O.;
Leverenz, James B.;
Weintraub, Daniel;
Trojanowski, John Q.;
Chen-Plotkin, Alice;
Van Deerlin, Vivianna M.;
Quinn, Joseph F.;
Chung, Kathryn A.;
Peterson-Hiller, Amie L.;
Rosenthal, Liana S.;
Dawson, Ted M.;
Albert, Marilyn S.;
Goldman, Jennifer G.;
Stebbins, Glenn T.;
Bernard, Bryan;
Wszolek, Zbigniew K.;
Ross, Owen A.;
Dickson, Dennis W.;
Eidelberg, David

Publication type:

Article

Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease.

Published in:

JAMA Neurology, 2015, v. 72, n. 1, p. 100, doi. 10.1001/jamaneurol.2014.2704

By:

Kalia, Lorraine V.;
Lang, Anthony E.;
Hazrati, Lili-Naz;
Fujioka, Shinsuke;
Wszolek, Zbigniew K.;
Dickson, Dennis W.;
Ross, Owen A.;
Van Deerlin, Vivianna M.;
Trojanowski, John Q.;
Hurtig, Howard I.;
Alcalay, Roy N.;
Marder, Karen S.;
Clark, Lorraine N.;
Gaig, Carles;
Tolosa, Eduardo;
Ruiz-Martínez, Javier;
Marti-Masso, Jose F.;
Ferrer, Isidre;
López de Munain, Adolfo;
Goldman, Samuel M.

Publication type:

Article

DCTN1 Mutations and Progressive Supranuclear Palsy-Like Phenotype.

Published in:

JAMA Neurology, 2014, v. 71, n. 5, p. 655, doi. 10.1001/jamaneurol.2014.227

By:

Fujioka, Shinsuke;
Tacik, Pawel;
Wszolek, Zbigniew K.

Publication type:

Article

Expanding the spectrum of KIF5A mutations—case report of a large kindred with familial ALS and overlapping syndrome.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2023, v. 24, n. 3/4, p. 347, doi. 10.1080/21678421.2022.2164204

By:

Dulski, JarosŁaw;
Strongosky, Audrey J.;
Al-Shaikh, Rana Hanna;
Wszolek, Zbigniew K.

Publication type:

Article

Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 5/6, p. 463, doi. 10.3109/21678421.2013.787630

By:

van Blitterswijk, Marka;
Baker, Matthew C.;
Bieniek, Kevin F.;
Knopman, David S.;
Josephs, Keith A.;
Boeve, Bradley;
Caselli, Richard;
Wszolek, Zbigniew K.;
Petersen, Ronald;
Graff-Radford, Neill R.;
Boylan, Kevin B.;
Dickson, Dennis W.;
Rademakers, Rosa

Publication type:

Article

Adult-onset leukodystrophies: a practical guide, recent treatment updates, and future directions.

Published in:

Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1219324

By:

Muthusamy, Karthik;
Sivadasan, Ajith;
Dixon, Luke;
Sudhakar, Sniya;
Thomas, Maya;
Danda, Sumita;
Wszolek, Zbigniew K.;
Wierenga, Klaas;
Dhamija, Radhika;
Gavrilova, Ralitza

Publication type:

Article

Neuropsychological profile of CSF1R-related leukoencephalopathy.

Published in:

Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1155387

By:

Rush, Beth K.;
Tipton, Philip W.;
Strongosky, Audrey;
Wszolek, Zbigniew K.

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

Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 9, p. 659, doi. 10.1038/sj.ejhg.5200698

By:

West, Andrew B;
Zimprich, Alexander;
Lockhart, Paul J;
Farrer, Matthew;
Singleton, Andrew;
Holtom, Benjamin;
Lincoln, Sarah;
Hofer, Anne;
Hill, Lori;
Müller-Myhsok, Bertram;
Wszolek, Zbigniew K;
Hardy, John;
Gasser, Thomas

Publication type:

Article

ALS-FTD Complex Disorder due to C9ORF72 Gene Mutation: Description of First Polish Family.

Published in:

European Neurology, 2014, v. 72, n. 1/2, p. 64, doi. 10.1159/000362267

By:

Siuda, Joanna;
Lewicka, Tatiana;
Bujak, Malgorzata;
Opala, Grzegorz;
Golenia, aleksandra;
Slowik, agnieszka;
van Blitterswijk, Marka;
Baker, Matt;
Ertekin-Taner, Nilufer;
Wszolek, Zbigniew K.;
Rademakers, Rosa

Publication type:

Article

Spinocerebellar ataxia type 3 (Machado-Joseph disease).

Published in:

Polish Archives of Internal Medicine, 2022, v. 132, n. 10, p. 1, doi. 10.20452/pamw.16322

By:

Dulski, Jarosław;
Al-Shaikh, Rana Hanna;
Sułek, Anna;
Kasprzak, Jakub;
Sławek, Jarosław;
Wszolek, Zbigniew K.

Publication type:

Article

Bioethics and informatics in medical studies during the coronavirus disease 2019 pandemic.

Published in:

Polish Archives of Internal Medicine, 2020, v. 130, n. 7/8, p. 719, doi. 10.20452/pamw.15474

By:

Williams, Unislawa M.;
Wszolek, Zbigniew K.

Publication type:

Article

Restless legs syndrome and nocturnal leg cramps: a review and guide to diagnosis and treatment.

Published in:

Polish Archives of Internal Medicine, 2017, v. 127, n. 12, p. 865, doi. 10.20452/pamw.4148

By:

Tipton, Philip W.;
Wszolek, Zbigniew K.

Publication type:

Article

Upper motor neuron‐predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological study.

Published in:

Brain Pathology, 2025, v. 35, n. 1, p. 1, doi. 10.1111/bpa.13286

By:

Murakami, Aya;
Koga, Shunsuke;
Fujioka, Shinsuke;
White, Adrianna E.;
Bieniek, Kevin F.;
Sekiya, Hiroaki;
DeJesus‐Hernandez, Mariely;
Finch, NiCole A.;
van Blitterswijk, Marka;
Nakamura, Masataka;
Tsuboi, Yoshio;
Murray, Melissa E.;
Wszolek, Zbigniew K.;
Dickson, Dennis W.

Publication type:

Article

Alpha‐synuclein‐associated changes in PINK1‐PRKN‐mediated mitophagy are disease context dependent.

Published in:

Brain Pathology, 2023, v. 33, n. 5, p. 1, doi. 10.1111/bpa.13175

By:

Hou, Xu;
Chen, Taylor Hsuan‐Yu;
Koga, Shunsuke;
Bredenberg, Jenny M.;
Faroqi, Ayman H.;
Delenclos, Marion;
Bu, Guojun;
Wszolek, Zbigniew K.;
Carr, Jonathan A.;
Ross, Owen A.;
McLean, Pamela J.;
Murray, Melissa E.;
Dickson, Dennis W.;
Fiesel, Fabienne C.;
Springer, Wolfdieter

Publication type:

Article

FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.

Published in:

Brain Pathology, 2017, v. 27, n. 5, p. 612, doi. 10.1111/bpa.12428

By:

Tacik, Pawel;
DeTure, Michael A.;
Carlomagno, Yari;
Lin, Wen‐Lang;
Murray, Melissa E.;
Baker, Matthew C.;
Josephs, Keith A.;
Boeve, Bradley F.;
Wszolek, Zbigniew K.;
Graff‐Radford, Neill R.;
Parisi, Joseph E.;
Petrucelli, Leonard;
Rademakers, Rosa;
Isaacson, Richard S.;
Heilman, Kenneth M.;
Petersen, Ronald C.;
Dickson, Dennis W.;
Kouri, Naomi

Publication type:

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

Acute measles encephalitis in adults.

Published in:

Journal of Neurology, 2006, v. 253, n. 1, p. 121, doi. 10.1007/s00415-005-0923-8

By:

Baba, Yasuhiko;
Tsuboi, Yoshio;
Inoue, Hirosato;
Yamada, Tatsuo;
Wszolek, Zbigniew K.;
Broderick, Daniel F.

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

Brain calcification in a CSF1R mutation carrier precedes white matter degeneration.

Published in:

2017

By:

Konno, Takuya;
Broderick, Daniel F.;
Wszolek, Zbigniew K.

Publication type:

Letter

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

Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.

Published in:

2017

By:

Sanchez‐Contreras, Monica;
Heckman, Michael G.;
Tacik, Pawel;
Diehl, Nancy;
Brown, Patricia H.;
Soto‐Ortolaza, Alexandra I.;
Christopher, Elizabeth A.;
Walton, Ronald L.;
Ross, Owen A.;
Golbe, Lawrence I.;
Graff‐Radford, Neill;
Wszolek, Zbigniew K.;
Dickson, Dennis W.;
Rademakers, Rosa

Publication type:

journal article

Primary familial brain calcification in the 'IBGC2' kindred: All linkage roads lead to SLC20A2.

Published in:

2016

By:

Grütz, Karen;
Volpato, Claudia B.;
Domingo, Aloysius;
Alvarez‐Fischer, Daniel;
Gebert, Uwe;
Schifferle, Günther;
Buffone, Ebba;
Wszolek, Zbigniew K.;
Rademakers, Rosa;
Ferbert, Andreas;
Hicks, Andrew A.;
Klein, Christine;
Pramstaller, Peter P.;
Westenberger, Ana

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

In vivo dopaminergic and serotonergic dysfunction in DCTN1 gene mutation carriers.

Published in:

Movement Disorders, 2014, v. 29, n. 9, p. 1197, doi. 10.1002/mds.25893

By:

Felicio, Andre C.;
Dinelle, Katherine;
Agarwal, Pankaj A.;
McKenzie, Jessamyn;
Heffernan, Nicole;
Road, Jeremy D.;
Appel‐Cresswell, Silke;
Wszolek, Zbigniew K.;
Farrer, Matthew J.;
Schulzer, Michael;
Sossi, Vesna;
Stoessl, A. Jon

Publication type:

Article

A novel de novo pathogenic mutation in the CACNA1A gene.

Published in:

Movement Disorders, 2012, v. 27, n. 12, p. 1578, doi. 10.1002/mds.25198

By:

Fujioka, Shinsuke;
Rayaprolu, Sruti;
Sundal, Christina;
Broderick, Daniel F.;
Langley, William A.;
Shoffner, John;
Hyams, Lauren C.;
Rademakers, Rosa;
Graff-Radford, Neill R.;
Tatum, William;
Ross, Owen A.;
Wszolek, Zbigniew K.

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

Dopamine turnover increases in asymptomatic LRRK2 mutations carriers.

Published in:

Movement Disorders, 2010, v. 25, n. 16, p. 2717, doi. 10.1002/mds.23356

By:

Sossi, Vesna;
de la Fuente-Fernández, Raul;
Nandhagopal, Ramachandiran;
Schulzer, Michael;
McKenzie, Jessamyn;
Ruth, Thomas J.;
Aasly, Jan O.;
Farrer, Matthew J.;
Wszolek, Zbigniew K.;
Stoessl, Jon A.

Publication type:

Article

LRRK2 variation and Parkinson's disease in African Americans.

Published in:

Movement Disorders, 2010, v. 25, n. 12, p. 1973, doi. 10.1002/mds.23163

By:

Ross, Owen A.;
Wilhoite, Greggory J.;
Bacon, Justin A.;
Soto-Ortolaza, Alexandra;
Kachergus, Jennifer;
Cobb, Stephanie A.;
Puschmann, Andreas;
Vilariño-Güell, Carles;
Farrer, Matthew J.;
Graff-Radford, Neill;
Meschia, James F.;
Wszolek, Zbigniew K.

Publication type:

Article

Adult-onset leg dystonia due to a missense mutation in THAP1.

Published in:

Movement Disorders, 2010, v. 25, n. 9, p. 1306, doi. 10.1002/mds.23086

By:

Van Gerpen, Jay A.;
LeDoux, Mark S.;
Wszolek, Zbigniew K.

Publication type:

Article

Clinical implications of gene discovery in Parkinson's disease and parkinsonism.

Published in:

Movement Disorders, 2010, v. 25, n. S1, p. S15, doi. 10.1002/mds.22723

By:

Wider, Christian;
Foroud, Tatiana;
Wszolek, Zbigniew K.

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

Corticobasal syndrome with Alzheimer's disease pathology.

Published in:

Movement Disorders, 2009, v. 24, n. 1, p. 152, doi. 10.1002/mds.21877

By:

Imamura, Akiko;
Wszolek, Zbigniew K.;
Lucas, John A.;
Dickson, Dennis W.

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