Soil-Embedded and Oil-Immersed Soil Stress Gage Calibration Tests von Dickson, Walton C, Windham, Jon E

Volltext bestellen

Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank von Bieniek, Kevin F., Ross, Owen A., Cormier, Kerry A., Walton, Ronald L., Soto-Ortolaza, Alexandra, Johnston, Amelia E., DeSaro, Pamela, Boylan, Kevin B., Graff-Radford, Neill R., Wszolek, Zbigniew K., Rademakers, Rosa, Boeve, Bradley F., McKee, Ann C., Dickson, Dennis W.

Volltext

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture von Sabir, Marya S., Bandres-Ciga, Sara, Saez-Atienzar, Sara, Reynolds, Regina H., Gustavsson, Emil, Ahmed, Sarah, Portley, Makayla K., Shah, Zalak, Abramzon, Yevgeniya, Hernandez, Dena G., Stone, David J., Eicher, John, Parkkinen, Laura, Honig, Lawrence S., Marder, Karen, Lemstra, Afina, St George-Hyslop, Peter, Morgan, Kevin, Lashley, Tammaryn, Warner, Thomas T., Jaunmuktane, Zane, Galasko, Douglas, Santana, Isabel, Myllykangas, Liisa, Oinas, Minna, Morris, John C., Van Deerlin, Vivianna M., Trojanowski, John Q., Grassano, Maurizio, Calvo, Andrea, Canosa, Antonio, Floris, Gianluca, Bohannan, Ryan C., Brett, Francesca, Gan-Or, Ziv, Geiger, Joshua T., Moore, Anni, Krüger, Rejko, Tayebi, Nahid, Sidransky, Ellen, Norcliffe-Kaufmann, Lucy, Newell, Kathy L., Gasser, Thomas, Schulte, Claudia, Landi, Francesco, Salvi, Erika, Masliah, Eliezer, Kim, Ronald C., Monuki, Edwin S., Brunetti, Maura, Pletnikova, Olga, Troncoso, Juan C., Flanagan, Margaret E., Infante, Jon, Lage, Carmen, Sanchez-Juan, Pascual, Black, Sandra E., Masellis, Mario, Rogaeva, Ekaterina, Duyckaerts, Charles, Brice, Alexis, Tilley, Bension S., Gentleman, Steve, McKeith, Ian G., Attems, Johannes, Morris, Christopher M., Palmer, Laura, Troakes, Claire, Hodges, Angela K., Klein, Gregory, Kaiser, Scott M., Woltjer, Randy, Pastor, Pau, Bekris, Lynn M., Besser, Lilah M., Renton, Alan E., Goate, Alison, Bennett, David A., Morris, Huw R., Ferrari, Raffaele, Pickering-Brown, Stuart, Kukull, Walter A., Morenas-Rodriguez, Estrella, Clarimon, Jordi, Nalls, Mike A., Ferrucci, Luigi, Resnick, Susan M., Tanaka, Toshiko, Foroud, Tatiana M., Graff-Radford, Neill R., Wszolek, Zbigniew K., Boeve, Bradley F., Topol, Eric J., Singleton, Andrew B., Dickson, Dennis W., Chiò, Adriano, Gibbs, J. Raphael, Dalgard, Clifton L., Traynor, Bryan J., Scholz, Sonja W.

Volltext

Decision‐making by the NICE Interventional Procedures Advisory Committee von Carroll, C., Dickson, R., Boland, A., Houten, R., Walton, M.

Volltext

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

Volltext

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

Volltext

Role of GBA variants in Lewy body disease neuropathology von Walton, Ronald L., Koga, Shunsuke, Beasley, Alexandra I., White, Launia J., Griesacker, Teresa, Murray, Melissa E., Kasanuki, Koji, Hou, Xu, Fiesel, Fabienne C., Springer, Wolfdieter, 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., Heckman, Michael G.

Volltext

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... von 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

Volltext

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

Volltext

Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degeneration von Koga, Shunsuke, Metrick, 2nd, 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

Volltext

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders von Ogaki, Kotaro, Koga, Shunsuke, Heckman, Michael G, Fiesel, Fabienne C, Ando, Maya, Labbé, Catherine, Lorenzo-Betancor, Oswaldo, Moussaud-Lamodière, Elisabeth L, Soto-Ortolaza, Alexandra I, Walton, Ronald L, Strongosky, Audrey J, Uitti, Ryan J, McCarthy, Allan, Lynch, Timothy, Siuda, Joanna, Opala, Grzegorz, Rudzinska, Monika, Krygowska-Wajs, Anna, Barcikowska, Maria, Czyzewski, Krzysztof, Puschmann, Andreas, Nishioka, Kenya, Funayama, Manabu, Hattori, Nobutaka, Parisi, Joseph E, Petersen, Ronald C, Graff-Radford, Neill R, Boeve, Bradley F, Springer, Wolfdieter, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A

Volltext

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

Volltext

Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease von Valentino, Rebecca R., Heckman, Michael G., Johnson, Patrick W., Baker, Matthew C., Soto-Beasley, Alexandra I., Walton, Ronald L., Koga, Shunsuke, Roemer, Shanu F., Suh, EunRan, Uitti, Ryan J., Trojanowski, John Q., Grossman, Murray, Van Deerlin, Vivianna M., Rademakers, Rosa, Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A.

Volltext

A novel tau mutation, p.K317N, causes globular glial tauopathy von Tacik, Pawel, DeTure, Michael, Lin, Wen-Lang, Sanchez Contreras, Monica, Wojtas, Aleksandra, Hinkle, Kelly M., Fujioka, Shinsuke, Baker, Matthew C., Walton, Ronald L., Carlomagno, Yari, Brown, Patricia H., Strongosky, Audrey J., Kouri, Naomi, Murray, Melissa E., Petrucelli, Leonard, Josephs, Keith A., Rademakers, Rosa, Ross, Owen A., Wszolek, Zbigniew K., Dickson, Dennis W.

Volltext

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies von Labbé, Catherine, Ogaki, Kotaro, Lorenzo-Betancor, Oswaldo, Soto-Ortolaza, Alexandra I, Walton, Ronald L, Rayaprolu, Sruti, Fujioka, Shinsuke, Murray, Melissa E, Heckman, Michael G, Puschmann, Andreas, McCarthy, Allan, Lynch, Timothy, Siuda, Joanna, Opala, Grzegorz, Rudzinska, Monika, Krygowska-Wajs, Anna, Barcikowska, Maria, Czyzewski, Krzysztof, Sanotsky, Yanosh, Rektorová, Irena, McLean, Pamela J, Rademakers, Rosa, Ertekin-Taner, Nilüfer, Hassan, Anhar, Ahlskog, J Eric, Boeve, Bradley F, Petersen, Ronald C, Maraganore, Demetrius M, Adler, Charles H, Ferman, Tanis J, Parisi, Joseph E, Graff-Radford, Neill R, Uitti, Ryan J, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A

Volltext

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

Volltext

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients von Lorenzo-Betancor, O., Ogaki, K., Soto-Ortolaza, A. I., Labbe, C., Walton, R. L., Strongosky, A. J., van Gerpen, J. A., Uitti, R. J., McLean, P. J., Springer, W., Siuda, J., Opala, G., Krygowska-Wajs, A., Barcikowska, M., Czyzewski, K., McCarthy, A., Lynch, T., Puschmann, A., Rektorova, I., Sanotsky, Y., Vilariño-Güell, C., Farrer, M. J., Ferman, T. J., Boeve, B. F., Petersen, R. C., Parisi, J. E., Graff-Radford, N. R., Dickson, D. W., Wszolek, Z. K., Ross, O. A.

Volltext

MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies von Labbé, Catherine, Heckman, Michael G, Lorenzo-Betancor, Oswaldo, Soto-Ortolaza, Alexandra I, Walton, Ronald L, Murray, Melissa E, Allen, Mariet, Uitti, Ryan J, Wszolek, Zbigniew K, Smith, Glenn E, Kantarci, Kejal, Knopman, David S, Lowe, Val J, Jack, Clifford R, Ertekin-Taner, Nilüfer, Hassan, Anhar, Savica, Rodolfo, Petersen, Ronald C, Parisi, Joseph E, Maraganore, Demetrius M, Graff-Radford, Neill R, Ferman, Tanis J, Boeve, Bradley F, Dickson, Dennis W, Ross, Owen A

Volltext

RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies von Hodges, Kyndall, Brewer, Sheridan S., Labbé, Catherine, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Strongosky, Audrey J., Uitti, Ryan J., van Gerpen, Jay A., Ertekin-Taner, Nilüfer, Kantarci, Kejal, Lowe, Val J., Parisi, Joseph E., Savica, Rodolfo, Graff-Radford, Jonathan, Jones, David T., Knopman, David S., Petersen, Ronald C., Murray, Melissa E., Graff-Radford, Neill R., Ferman, Tanis J., Dickson, Dennis W., Wszolek, Zbigniew K., Boeve, Bradley F., Ross, Owen A., Lorenzo-Betancor, Oswaldo

Volltext

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

Volltext