Dancing Feet Dyskinesia in a Patient with GBA-PD

por Olszewska, Diana A., McCarthy, Allan, Soto-Beasley, Alexandra I., Walton, Ronald L., Ross, Owen A., Lynch, Tim
Publicado 2022

Effects of buprenorphine in the adrenal, thyroid, and cytokine intra-operative responses in a rat model (Rattus norvegicus): a preliminary study

por Félix, Nuno M, Leal, Rodolfo O, Goy-Thollot, I, Walton, Ronald S, Gil, Solange A, Mateus, Luísa M, Matos, Ana S, Niza, Maria M R E
Publicado 2017

Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

por Koga, Shunsuke, Murakami, Aya, Soto-Beasley, Alexandra I., Walton, Ronald L., Baker, Matthew C., Castanedes-Casey, Monica, Josephs, Keith A., Ross, Owen A., Dickson, Dennis W.
Publicado 2023

Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS path...

por Koga, Shunsuke, Murakami, Aya, Soto-Beasley, Alexandra I., Walton, Ronald L., Baker, Matthew C., Castanedes-Casey, Monica, Josephs, Keith A., Ross, Owen A., Dickson, Dennis W.
Publicado 2023

Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland

por Olszewska, Diana A., McCarthy, Allan, Soto-Beasley, Alexandra I., Walton, Ronald L., Magennis, Brian, McLaughlin, Russell L., Hardiman, Orla, Ross, Owen A., Lynch, Tim
Publicado 2020

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

por Deutschlander, Angela B., Konno, Takuya, Soto‐Beasley, Alexandra I., Walton, Ronald L., van Gerpen, Jay A., Uitti, Ryan J., Heckman, Michael G., Wszolek, Zbigniew K., Ross, Owen A.
Publicado 2020

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

por 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.
Publicado 2020

Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease

por Koga, Shunsuke, Li, Fuyao, Zhao, Na, Roemer, Shanu F., Ferman, Tanis J., Wernick, Anna I., Walton, Ronald L., Faroqi, Ayman H., Graff‐Radford, Neill R., Cheshire, William P., Ross, Owen A., Dickson, Dennis W.
Publicado 2020

Early-Onset Parkinson Disease Screening in Patients From Nigeria

por Milanowski, Lukasz M., Oshinaike, Olajumoke, Broadway, Benjamin J., Lindemann, Jennifer A., Soto-Beasley, Alexandra I., Walton, Ronald L., Hanna Al-Shaikh, Rana, Strongosky, Audrey J., Fiesel, Fabienne C., Ross, Owen A., Springer, Wolfdieter, Ogun, Shamsideen Abayomi, Wszolek, Zbigniew K.
Publicado 2021

Analysis of COQ2 gene in multiple system atrophy

por Ogaki, Kotaro, Fujioka, Shinsuke, Heckman, Michael G, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Labbé, Catherine, Walton, Ronald L, Lorenzo-Betancor, Oswaldo, Wang, Xue, Asmann, Yan, Rademakers, Rosa, Graff-Radford, Neill, Uitti, Ryan, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A
Publicado 2014

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

por 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.
Publicado 2020

Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degeneration

por Koga, Shunsuke, Metrick, Michael A., Golbe, Lawrence I., Santambrogio, Alessia, Kim, Minji, Soto-Beasley, Alexandra I., Walton, Ronald L., Baker, Matthew C., De Castro, Cristhoper Fernandez, DeTure, Michael, Russell, David, Navia, Bradford A., Sandiego, Christine, Ross, Owen A., Vendruscolo, Michele, Caughey, Byron, Dickson, Dennis W.
Publicado 2023

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

por 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.
Publicado 2015

Association study between multiple system atrophy and TREM2 p.R47H

por Ogaki, Kotaro, Heckman, Michael G., Koga, Shunsuke, Martens, Yuka A., Labbé, Catherine, Lorenzo-Betancor, Oswaldo, Walton, Ronald L., Soto, Alexandra I., Vargas, Emily R., Fujioka, Shinsuke, Uitti, Ryan J., van Gerpen, Jay A., Cheshire, William P., Younkin, Steven G., Wszolek, Zbigniew K., Low, Phillip A., Singer, Wolfgang, Bu, Guojun, Dickson, Dennis W., Ross, Owen A.
Publicado 2018

Mitophagy alterations in Alzheimer's disease are associated with granulovacuolar degeneration and early tau pathology

por Hou, Xu, Watzlawik, Jens O., Cook, Casey, Liu, Chia‐Chen, Kang, Silvia S., Lin, Wen‐Lang, DeTure, Michael, Heckman, Michael G., Diehl, Nancy N., Al‐Shaikh, Fadi S. Hanna, Walton, Ronald L., Ross, Owen A., Melrose, Heather L., Ertekin‐Taner, Nilüfer, Bu, Guojun, Petrucelli, Leonard, Fryer, John D., Murray, Melissa E., Dickson, Dennis W., Fiesel, Fabienne C., Springer, Wolfdieter
Publicado 2020

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

por 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., Wszolek, Zbigniew K., Ross, Owen A., Graff-Radford, Neill R., Dickson, Dennis W., Ertekin-Taner, Nilüfer
Publicado 2020

ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans

por Conway, Olivia J, Carrasquillo, Minerva M, Wang, Xue, Bredenberg, Jenny M, Reddy, Joseph S, Strickland, Samantha L, Younkin, Curtis S, Burgess, Jeremy D, Allen, Mariet, Lincoln, Sarah J, Nguyen, Thuy, Malphrus, Kimberly G, Soto, Alexandra I, Walton, Ronald L, Boeve, Bradley F, Petersen, Ronald C, Lucas, John A, Ferman, Tanis J, Cheshire, William P, van Gerpen, Jay A, Uitti, Ryan J, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Ertekin-Taner, Nilüfer
Publicado 2018

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies

por Walton, Ronald L., Soto-Ortolaza, Alexandra I., Murray, Melissa E., Lorenzo-Betancor, Oswaldo, Ogaki, Kotaro, Heckman, Michael G., Rayaprolu, Sruti, Rademakers, Rosa, Ertekin-Taner, Nilüfer, Uitti, Ryan J., van Gerpen, Jay A., Wszolek, Zbigniew K., Smith, Glenn E., Kantarci, Kejal, Lowe, Val J., Parisi, Joseph E., Jones, David T., Savica, Rodolfo, Graff-Radford, Jonathan, Knopman, David S., Petersen, Ronald C., Graff-Radford, Neill R., Ferman, Tanis J., Dickson, Dennis W., Boeve, Bradley F., Ross, Owen A., Labbé, Catherine
Publicado 2016

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

por 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., Parisi, Joseph E., Reichard, R. Ross, Graff-Radford, Neill R., Ferman, Tanis J., Boeve, Bradley F., Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A.
Publicado 2022

Cathepsin B p.Gly284Val Variant in Parkinson’s Disease Pathogenesis

por Milanowski, Lukasz M., Hou, Xu, Bredenberg, Jenny M., Fiesel, Fabienne C., Cocker, Liam T., Soto-Beasley, Alexandra I., Walton, Ronald L., Strongosky, Audrey J., Faroqi, Ayman H., Barcikowska, Maria, Boczarska-Jedynak, Magdalena, Dulski, Jaroslaw, Fedoryshyn, Lyuda, Janik, Piotr, Potulska-Chromik, Anna, Karpinsky, Katherine, Krygowska-Wajs, Anna, Lynch, Tim, Olszewska, Diana A., Opala, Grzegorz, Pulyk, Aleksander, Rektorova, Irena, Sanotsky, Yanosh, Siuda, Joanna, Widlak, Mariusz, Slawek, Jaroslaw, Rudzinska-Bar, Monika, Uitti, Ryan, Figura, Monika, Szlufik, Stanislaw, Rzonca-Niewczas, Sylwia, Podgorska, Elzbieta, McLean, Pamela J., Koziorowski, Dariusz, Ross, Owen A., Hoffman-Zacharska, Dorota, Springer, Wolfdieter, Wszolek, Zbigniew K.
Publicado 2022