Zobrazeno 71 - 80
of 286
pro vyhledávání: '"Vivianna, M Van Deerlin"'
Autor:
Debby W. Tsuang, Walter A. Kukull, Vivianna M. Van Deerlin, Dora Yearout, Sharon X. Xie, James B. Leverenz, J. A. Kaye, Katelan Longfellow, Randy Woltjer, Howard I. Hurtig, Thomas J. Montine, Oscar L. Lopez, Gregory A. Jicha, C. Dirk Keene, John E. Duda, Joseph F. Quinn, Cyrus P. Zabetian, Murray Grossman, Daniel Weintraub, Peter T. Nelson, John Q. Trojanowski, David J. Irwin, Julia Kofler, Edward B. Lee
Publikováno v:
The Lancet Neurology. 16:55-65
Great heterogeneity exists in survival and the interval between onset of motor symptoms and dementia symptoms across synucleinopathies. We aimed to identify genetic and pathological markers that have the strongest association with these features of c
Autor:
Sílvia Porta, David J. Irwin, Boram Kim, Aivi T. Nguyen, Lakshmi Changolkar, Jessica M. Phan, Corey T. McMillan, Geoffrey K. Aguirre, Edward B. Lee, Kelvin C. Luk, Camilo Toro, Garrett S. Gibbons, Vivianna M. Van Deerlin, Sokratis G. Papageorgiou, Lauren Massimo, John Papatriantafyllou, Ilya M. Nasrallah, EunRan Suh, Murray Grossman, Nabil F. Darwich, Caroline M. O’Rourke, Zhuohao He
Publikováno v:
Science
Two ways to get tangled? Neurodegeneration in Alzheimer's disease dementia is associated with neurofibrillary tangles composed of aggregated tau protein. Darwich et al. describe an additional form of autosomal-dominant dementia with neurofibrillary t
Autor:
Camilo Toro, David J. Irwin, EunRan Suh, Jessica M. Phan, Edward B. Lee, G.K. Aguirre, Corey T. McMillan, Nabil F. Darwich, Murray Grossman, Vivianna M. Van Deerlin
Publikováno v:
Alzheimer's & Dementia. 15
Autor:
Wan Yun Ho, Claire Troakes, Edward B. Lee, Hans A. Kretzschmar, Charles L. White, Virginia M.-Y. Lee, Helen Ling, Christopher P. Cali, Catriona McLean, Jean Paul Vonsattel, Bernardino Ghetti, Juan C. Troncoso, Gerard D. Schellenberg, Shuo-Chien Ling, Kin Y. Mok, Maribel Patino, John Q. Trojanowski, Sigrun Roeber, William W. Seeley, Dennis W. Dickson, Vivianna M. Van Deerlin, Bruce L. Miller, Marla Gearing, Carles Gaig, Yee Kit Tai, Christopher Morris
Publikováno v:
Acta Neuropathol
Acta neuropathologica, vol 138, iss 5
Acta neuropathologica, vol 138, iss 5
Microsatellite repeat expansion disease loci can exhibit pleiotropic clinical and biological effects depending on repeat length. Large expansions in C9orf72 (100s-1000s of units) are the most common genetic cause of amyotrophic lateral sclerosis (ALS
Autor:
Sharon X. Xie, John Q. Trojanowski, Daniel Weintraub, David J. Irwin, Michael H Guo, Andrew Siderowf, Vivianna M. Van Deerlin, David A. Wolk, Jordan T. Mak, EunRan Suh, Alice Chen-Plotkin, Jacqueline Rick, Murray Grossman, Thomas F. Tropea
Publikováno v:
Ann Neurol
Objective Common variants near TMEM106B associate with risk of developing frontotemporal dementia (FTD). Emerging evidence suggests a role for TMEM106B in neurodegenerative processes beyond FTD. We evaluate the effect of TMEM106B genotype on cognitiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8a76bbe588efcfc4e839e286361b706
https://europepmc.org/articles/PMC6953172/
https://europepmc.org/articles/PMC6953172/
Autor:
David P. Breen, Samantha J. Hutten, Alastair J. Noyce, Dena G. Hernandez, Kumaraswamy Naidu Chitrala, Lasse Pihlstrøm, Jacqueline Rick, Mathias Toft, Mike A. Nalls, Ganqiang Liu, Karol Estrada, Jean-Christophe Corvol, Marlies van Nimwegen, Bernard Ravina, Shirley Eberly, Aaron G. Day-Williams, Jonathan R. Evans, Peter Heutink, Claire E. Wegel, Ole-Bjørn Tysnes, J. Raphael Gibbs, Bart P.C. van de Warrenburg, Peggy Auinger, Alexis Brice, Hirotaka Iwaki, Clemens R. Scherzer, Jonggeol J. Kim, Jodi Maple-Grødem, Kirsten M. Scott, Fabrice Danjou, Daniel Weintraub, H. Nguyen Khanh-Dung, Jacobus J. van Hilten, Roger A. Barker, Caroline H. Williams-Gray, Hampton L. Leonard, Cornelis Blauwendraat, David Simon, Andrew B. Singleton, Faraz Faghri, Guido Alves, Ruwani Wijeyekoon, Ole A. Andreassen, Vivianna M. Van Deerlin, Bastiaan R. Bloem
BackgroundSeveral reports have identified different patterns of Parkinson’s disease progression in individuals carrying missense variants in theGBAorLRRK2genes. The overall contribution of genetic factors to the severity and progression of Parkinso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63e500b2bfcbaa1c99a721afb2cb6777
Autor:
EunRan Suh, Carrie Caswell, Virginia M.-Y. Lee, John Q. Trojanowski, Murray Grossman, Vivianna M. Van Deerlin, David J. Irwin, Edward B. Lee, Sharon X. Xie, Lauren Massimo, Corey T. McMillan
Publikováno v:
Neurology
ObjectiveTo determine autosomal dominant genetic predictors of survival in individuals with behavioral variant frontotemporal degeneration (bvFTD).MethodsA retrospective chart review of 174 cases with a clinical phenotype of bvFTD but no associated e
Autor:
Nigel J. Cairns, Merel O. Mol, Gregory D. Jenkins, Leonard Petrucelli, Nilufer Ertekin-Taner, Stuart Pickering-Brown, Carlos Cruchaga, Edward B. Lee, Jonathan D. Glass, John C. van Swieten, Jonathan D. Rohrer, Keith A. Josephs, Patrizia Rizzu, Johannes Prudlo, Edward D. Huey, Cristina T. Vicente, Shulan Tian, Claire Troakes, Ging-Yuek Robin Hsiung, Julie S. Snowden, Lawrence S. Honig, Jean Paul G. Vonsattel, Yan W. Asmann, Matthis Synofzik, Sigrun Roeber, Jeroen van Rooij, Ralph B. Perkerson, Eric M. Reiman, Charles L. White, Ethan G. Geier, Billie J. Matchett, Robert A. Rissman, Julia Keith, David J. Irwin, Manuela Neumann, Dieter Edbauer, M.-Marsel Mesulam, Jochen Herms, Vivianna M. Van Deerlin, Jordan Grafman, Melissa E. Murray, Oscar L. Lopez, Bernardino Ghetti, Rosa Rademakers, Bradley F. Boeve, Ekaterina Rogaeva, Sara Rollinson, Marla Gearing, Geoffrey L. Ahern, Zachary C. Fogarty, Peter Heutink, Yingxue Ren, Javier Simón-Sánchez, David G. Mann, Bryan K. Woodruff, Ryan J. Uitti, Martin R. Farlow, Lea T. Grinberg, Murray Grossman, Julia Kofler, Ian R. A. Mackenzie, Jennifer S. Yokoyama, Lorne Zinman, Matt Baker, John Q. Trojanowski, Zbigniew K. Wszolek, Cyril Pottier, Changiz Geula, Thomas Arzberger, Dennis W. Dickson, Joanna M. Biernacka, William W. Seeley, Caroline Graff, Olivier Piguet, John B.J. Kwok, Joseph E. Parisi, Safa Al-Sarraj, Harro Seelaar, Elizabeth Christopher, Ronald C. Petersen, Linn Öijerstedt, Anna Karydas, Salvatore Spina, Carlo Wilke, Marka van Blitterswijk, Simon Mead, Janine Diehl-Schmid, Bret M. Evers, David S. Knopman, Kevin F. Bieniek, John R. Hodges, Anthony Batzler, Mariely DeJesus-Hernandez, Elizabeth Finger, Thomas G. Beach, EunRan Suh, Maria Carmela Tartaglia, Sandra Weintraub, Shannon K. McDonnell, Bruce L. Miller, Glenda M. Halliday, Andy King, Eileen H. Bigio, Neill R. Graff-Radford, Richard J. Caselli
Publikováno v:
Acta Neuropathologica, 137(6), 879-899. Springer-Verlag
Acta Neuropathol
Acta neuropathologica 137(6), 879-899 (2019). doi:10.1007/s00401-019-01962-9
Acta neuropathologica
Acta Neuropathol
Acta neuropathologica 137(6), 879-899 (2019). doi:10.1007/s00401-019-01962-9
Acta neuropathologica
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-TDP) represents the most common pathological subtype of FTLD. We established the international FTLD-TDP whole-genome sequencing consortium to thoroughl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1500c504ddc41a67b8cb5e111941d5d5
https://pure.eur.nl/en/publications/ec4efc7a-1a6b-4346-af9a-7b821d069c4d
https://pure.eur.nl/en/publications/ec4efc7a-1a6b-4346-af9a-7b821d069c4d
Autor:
Sonja W. Scholz, Pentti J. Tienari, Dena G. Hernandez, Elisabet Londos, Alberto Lleó, Imelda Barber, Jose Bras, Owen A. Ross, Tanis J. Ferman, Tatiana Orme, Juan C. Troncoso, Andrew B. Singleton, John D. Eicher, John Hardy, Karen Marder, Tammaryn Lashley, Douglas Galasko, Liisa Myllykangas, Ted M. Dawson, Eliezer Masliah, David M. A. Mann, Ekaterina Rogaeva, Stuart Pickering-Brown, Monica Diez-Fairen, Claire Troakes, Peter St George-Hyslop, Nigel J. Cairns, Dennis W. Dickson, Lee Darwent, Thomas G. Beach, David J. Stone, Olga Pletnikova, Glenda M. Halliday, Jordi Clarimón, John Q. Trojanowski, Anne Braae, Claire E. Shepherd, Pau Pastor, Geidy E. Serrano, Susana Carmona, Minna Oinas, Andrew J. Lees, Afina W. Lemstra, Miquel Aguilar, Laura Parkkinen, Rita Guerreiro, Estrella Morenas-Rodríguez, Janice L. Holton, Olaf Ansorge, Tamas Revesz, Vivianna M. Van Deerlin, Neill R. Graff-Radford, Safa Al-Sarraj, Kristelle Brown, Valentina Escott-Price, Suzanne Lesage, Lawrence S. Honig, Celia Kun-Rodrigues, John C. Morris, Ronald C. Petersen, Henrik Zetterberg, Kevin Morgan, Brad F. Boeve, Lorraine N. Clark, Isabel Santana, Yaroslau Compta, Liana S. Rosenthal, Michael G. Heckman
Publikováno v:
Kun-Rodrigues, C, Orme, T, Carmona, S, Hernandez, D G, Ross, O A, Eicher, J D, Shepherd, C, Parkkinen, L, Darwent, L, Heckman, M G, Scholz, S W, Troncoso, J C, Pletnikova, O, Dawson, T, Rosenthal, L, Ansorge, O, Clarimon, J, Lleo, A, Morenas-Rodriguez, E, Clark, L, Honig, L S, Marder, K, Lemstra, A, Rogaeva, E, St. George-Hyslop, P, Londos, E, Zetterberg, H, Barber, I, Braae, A, Brown, K, Morgan, K, Troakes, C, Al-Sarraj, S, Lashley, T, Holton, J, Compta, Y, van Deerlin, V, Serrano, G E, Beach, T G, Lesage, S, Galasko, D, Masliah, E, Santana, I, Pastor, P, Diez-Fairen, M, Aguilar, M, Tienari, P J, Myllykangas, L, Oinas, M, Revesz, T, Lees, A, Boeve, B F, Petersen, R C, Ferman, T J, Escott-Price, V, Graff-Radford, N, Cairns, N J, Morris, J C, Pickering-Brown, S, Mann, D, Halliday, G M, Hardy, J, Trojanowski, J Q, Dickson, D W, Singleton, A, Stone, D J, Guerreiro, R & Bras, J 2019, ' A comprehensive screening of copy number variability in dementia with Lewy bodies ', Neurobiology of Aging, vol. 75, pp. 223.e1-223.e10 . https://doi.org/10.1016/j.neurobiolaging.2018.10.019
Neurobiology of aging 75, 223.e1-223.e10 (2019). doi:10.1016/j.neurobiolaging.2018.10.019
Neurobiology of Aging, 75, 223.e1-223.e10. Elsevier Inc.
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging 75, 223.e1-223.e10 (2019). doi:10.1016/j.neurobiolaging.2018.10.019
Neurobiology of Aging, 75, 223.e1-223.e10. Elsevier Inc.
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
The role of genetic variability in dementia with Lewy bodies (DLB) is now indisputable; however, data regarding copy number variation (CNV) in this disease has been lacking. Here, we used whole-genome genotyping of 1454 DLB cases and 1525 controls to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fe78b5077a5e0a2df60bae68e7079cb
https://hdl.handle.net/10400.4/2247
https://hdl.handle.net/10400.4/2247
Autor:
Roy D. Bloom, Pavan Atluri, Nicole Hornsby, Matthew H. Levine, Katharine J. Bar, Paige M. Porrett, Richard Hasz, Vivianna M. Van Deerlin, Christian A. Bermudez, Peter P. Reese, Anna Sicilia, Lawrence Suplee, Ashley Woodards, Emily A. Blumberg, Michael A. Acker, Muhammad N. Zahid, K. Rajender Reddy, Jennifer R. Smith, Caren Gentile, Lee R. Goldberg, Rhondalyn C. McLean, David S. Goldberg, Peter L. Abt
Publikováno v:
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant SurgeonsREFERENCES. 19(9)
The advent of direct-acting antiviral therapy for hepatitis C virus (HCV) has generated tremendous interest in transplanting organs from HCV-infected donors. We conducted a single-arm trial of orthotopic heart transplantation (OHT) from HCV-infected