Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vivianna, M Van Deerlin"'
Autor:
Nabila Dahodwala, Alice Chen-Plotkin, Sharon X. Xie, Jacqueline Rick, Lana M. Chahine, Leslie M. Shaw, John Q. Trojanowski, Daniel Weintraub, Thomas F. Tropea, Jimit Doshi, Vivianna M. Van Deerlin, Christos Davatzikos
Publikováno v:
Movement Disorders. 33:289-297
BACKGROUND People with PD are at high risk of developing cognitive impairment and dementia. Cross-sectional studies have identified candidate biomarkers associated with cognitive decline. However, longitudinal studies on this topic are rarer, and few
Autor:
Marilyn S. Albert, Brenna Cholerton, Johnna Devoto, Kathryn A. Chung, Alice Chen-Plotkin, Ignacio F. Mata, Jennifer G. Goldman, Debby W. Tsuang, Glenn T. Stebbins, Fredy J. Revilla, John Q. Trojanowski, James B. Leverenz, Cathy Wood-Siverio, Liana S. Rosenthal, Joseph F. Quinn, Thomas J. Montine, Daniel Weintraub, Cyrus P. Zabetian, Rebecca Rausch, Shu Ching Hu, Alberto J. Espay, Bryan Bernard, Karen L. Edwards, Ted M. Dawson, Haley Huston, Beate Ritz, Vivianna M. Van Deerlin, Stewart A. Factor, Amie L. Peterson-Hiller, Dora Yearout
Publikováno v:
Movement Disorders. 31:95-102
Background Loss-of-function mutations in the GBA gene are associated with more severe cognitive impairment in PD, but the nature of these deficits is not well understood and whether common GBA polymorphisms influence cognitive performance in PD is no
Autor:
Kathryn A. Chung, Jennifer G. Goldman, Catherine O. Johnson, Joseph F. Quinn, Alberto J. Espay, Karen L. Edwards, Brenna Cholerton, Vivianna M. Van Deerlin, Stewart A. Factor, Johnna Devoto, Amie Peterson, Fredy J. Revilla, Thomas J. Montine, Daniel Weintraub, Marilyn S. Albert, Cathy Wood-Siverio, Rebecca Rausch, Shu Ching Hu, Ignacio F. Mata, Glenn T. Stebbins, John Q. Trojanowski, Zbigniew K. Wszolek, James B. Leverenz, Sindhu Srivatsal, Beate Ritz, Jing Zhang, Kathleen S. Montine, Liana S. Rosenthal, Ted M. Dawson, Bryan Bernard, Ryan J. Uitti, Cyrus P. Zabetian, Dennis W. Dickson
Publikováno v:
Movement Disorders. 30:728-733
Author(s): Srivatsal, S; Cholerton, B; Leverenz, JB; Wszolek, ZK; Uitti, RJ; Dickson, DW; Weintraub, D; Trojanowski, JQ; Van Deerlin, VM; Quinn, JF; Chung, KA; Peterson, AL; Factor, SA; Wood-Siverio, C; Goldman, JG; Stebbins, GT; Bernard, B; Ritz, B;
Autor:
Ali Samii, John Q. Trojanowski, Christine R. Swanson, John W. Roberts, Rachel Goldmann Gross, Pinky Agarwal, Howard I. Hurtig, Kathy Li, Travis L. Unger, Daniel Weintraub, Michael D. Gallagher, Jacqueline Rick, Alice Chen-Plotkin, Cyrus P. Zabetian, Vivianna M. Van Deerlin, James B. Leverenz
Publikováno v:
Movement Disorders. 30:805-812
The discovery of novel plasma-based biomarkers could lead to new approaches in the treatment of Parkinson's disease (PD). Here, we explore the role of plasma apolipoprotein A1 (ApoA1) as a risk marker for PD and evaluate the influence of APOA1 promot
Autor:
María Sierra, Erica Martinez, Kathryn A. Chung, Pinky Agarwal, Carolyn M. Hutter, Joseph F. Quinn, Karen L. Edwards, Oswaldo Lorenzo-Betancor, Amy Colcher, Jon Infante, Pau Pastor, Victoria Alvarez, Hojoong M. Kim, Renee Ribacoba, John W. Roberts, Pilar Gómez-Garre, Jia Y. Wan, Dora Yearout, Beate Ritz, Shannon L. Rhodes, Vivianna M. Van Deerlin, Pablo Mir, Ali Samii, Cyrus P. Zabetian, Federico M. Farin, Ignacio F. Mata, Harvey Checkoway
Publikováno v:
Movement Disorders. 27:1823-1826
Background Common variants in the LRRK2 gene influence risk of Parkinson’s disease (PD) in Asians, but whether the same is true in European-derived populations is less clear.
Autor:
Alice Chen-Plotkin, Sharon X. Xie, Nabila Dahodwala, Andrew Siderowf, Amy Colcher, Stacy Horn, John E. Duda, Vivianna M. Van Deerlin, Matthew B. Stern, Daniel Weintraub, Howard I. Hurtig, James F. Morley, Dana Falcone
Publikováno v:
Movement Disorders. 27:512-518
The role of genetic factors in cognitive decline associated with Parkinson's disease (PD) is unclear. We examined whether variations in apolipoprotein E (APOE), microtubule-associated protein tau (MAPT), or catechol-O-methytransferase (COMT) genotype
Autor:
Wuxing Yuan, Benoit I. Giasson, Jason P. Covy, Elisa A. Waxman, Howard I. Hurtig, Vivianna M. Van Deerlin
Publikováno v:
Movement Disorders. 24:32-39
Mutations in LRRK2 are the single most common known cause of Parkinson's disease (PD). Two new PD patients with LRRK2 mutation were identified from a cohort with extensive postmortem assessment. One of these patients harbors the R793M mutation and pr