Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Kimberly A. Quaid"'
Autor:
Stephan Müller, Oliver Preische, Hamid R. Sohrabi, Susanne Gräber, Mathias Jucker, Janko Dietzsch, John M. Ringman, Ralph N. Martins, Eric McDade, Peter R. Schofield, Bernardino Ghetti, Martin Rossor, Neill R. Graff-Radford, Johannes Levin, Douglas Galasko, Kimberly A. Quaid, Stephen Salloway, Chengjie Xiong, Tammie Benzinger, Virginia Buckles, Colin L. Masters, Reisa Sperling, Randall J. Bateman, John C. Morris, Christoph Laske
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract The relationship between body-mass index (BMI) and Alzheimer´s disease (AD) has been extensively investigated. However, BMI alterations in preclinical individuals with autosomal dominant AD (ADAD) have not yet been investigated. We analyzed
Externí odkaz:
https://doaj.org/article/5827ec97abdf4b4b9ad4e8fcc030acca
Autor:
Eric M. Meslin, Joshua B. Rager, Peter H. Schwartz, Kimberly A. Quaid, Margaret M. Gaffney, Jon Duke, William M. Tierney
Publikováno v:
Clinical and Translational Medicine, Vol 4, Iss 1, Pp n/a-n/a (2015)
AbstractRelationships between industry and university‐based researchers have been commonplace for decades and have received notable attention concerning the conflicts of interest these relationships may harbor. While new efforts are being made to u
Externí odkaz:
https://doaj.org/article/c3f4df1fe0af47d4aad38d55b5d779b5
Autor:
Buckles, Randall J. Bateman, Hiroshi Mori, Ricardo F. Allegri, Bernardino Ghetti, Katrina L. Paumier, Christoph Laske, Soheyl Noachtar, Jasmeer P. Chhatwal, Nick C. Fox, Adrian Danek, James M. Noble, Jonathan Vöglein, Peter R. Schofield, Stephen Salloway, Colin L. Masters, Johannes Levin, Mathias Jucker, Kimberly A. Quaid, Sarah B. Berman, John M. Ringman, John C. Morris, Martin N. Rossor, Eric McDade, Reisa A. Sperling
Publikováno v:
Neurobiology of aging 76, 18-23 (2019). doi:10.1016/j.neurobiolaging.2018.11.022
Our objective was to assess the reported history of seizures in cognitively asymptomatic mutation carriers for autosomal dominant Alzheimer's disease (ADAD) and the predictive value of seizures for mutation carrier status in cognitively asymptomatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::955bc2a86643a735efbf2a69929d6d23
https://europepmc.org/articles/PMC6572755/
https://europepmc.org/articles/PMC6572755/
Publikováno v:
Clinical Genetics. 91:824-831
Huntington disease (HD) is a late onset ultimately fatal neurodegenerative disorder caused by a cytosine-adenine-guanine ( CAG) triplet repeat expansion in the Huntingtin gene which was discovered in 1993. The PHAROS study is a unique observational s
Autor:
Ira Shoulson, Rebecca E. Ready, Stacey K. Barton, Jane S. Paulsen, Stephen M. Rao, Julie C. Stout, Elizabeth A. Hahn, Stephen G. Schilling, Noelle E. Carlozzi, Michael D. Geschwind, Susan Perlman, Jennifer A. Miner, Martha Nance, Christopher A. Ross, Anna L. Kratz, Kimberly A. Quaid, Jin Shei Lai, Praveen Dayalu, H. Marin, Michael K. McCormack, Siera Goodnight, Nancy R. Downing, Joel S. Perlmutter, Samuel Frank, Richard Gershon, David Cella
Publikováno v:
Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, vol 25, iss 10
Carlozzi, NE; Schilling, SG; Lai, J-S; Paulsen, JS; Hahn, EA; Perlmutter, JS; et al.(2016). HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD). QUALITY OF LIFE RESEARCH, 25(10), 2441-2455. doi: 10.1007/s11136-016-1386-3. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2nb8m503
Carlozzi, NE; Schilling, SG; Lai, J-S; Paulsen, JS; Hahn, EA; Perlmutter, JS; et al.(2016). HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD). QUALITY OF LIFE RESEARCH, 25(10), 2441-2455. doi: 10.1007/s11136-016-1386-3. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2nb8m503
PurposeHuntington disease (HD) is a chronic, debilitating genetic disease that affects physical, emotional, cognitive, and social health. Existing patient-reported outcomes (PROs) of health-related quality of life (HRQOL) used in HD are neither compr
Autor:
Stephen G. Schilling, Noelle E. Carlozzi, Michael K. McCormack, Elizabeth A. Hahn, Jennifer A. Miner, Martha Nance, Jin Shei Lai, Samuel Frank, Siera Goodnight, Kimberly A. Quaid, Nancy R. Downing, Jane S. Paulsen, Joel S. Perlmutter, David Cella
Publikováno v:
Quality of Life Research. 25:2403-2415
Huntington disease (HD) is an incurable terminal disease. Thus, end of life (EOL) concerns are common in these individuals. A quantitative measure of EOL concerns in HD would enable a better understanding of how these concerns impact health-related q
Autor:
William Mallonee, Thomas T. Warner, Vicki L. Wheelock, Emily P. Freney, Stephen M. Rao, Vincent A. Magnotta, Alma Macaraeg, Sigurd D. Süßmuth, Paula Wasserman, Shineeka Smith, Phil Danzer, Anne Elizabeth Rosser, Michael D. Geschwind, Brenton Maxwell, Kelsey Montross, Gabriella Satris, Albie Law, Daniel S. O'Leary, David J. Moser, Thomas Brashers-Krug, Janessa O. Carvalho, Hans J. Johnson, Martha Nance, Anita M.Y. Goh, Mark Guttman, J. Preston, Janet K. Williams, Judith Bek, Susan Perlman, Alanna Sheinberg, Wenjing Lu, Christine Reece, Pietro Mazzoni, Nadine Yoritomo, Elizabeth Aylward, W.R. Wayne Martin, Megan M. Smith, Phyllis Chua, J. Decolongon, Breanna Nickels, Pamela King, Deborah L. Harrington, Roland Zschiegner, Brian Clemente, David G. Gunn, Alex Bura, Vivien Vaughan, Samantha M Loi, Maggie Burrows, Kimberly A. Quaid, Jillian McMillan, Jason Evans, Michael Orth, Mary Wodarski, Courtney Shadrick, Sarah L Mason, H. Jeremy Bockholt, Marguerite Wieler, Elizabeth Howard, Melissa Wesson, Kathy Price, Lisa Kjer, Daniela Rae, Lynn A. Raymond, Roger A. Barker, Edmond Chiu, Holly Westervalt, Joanne Wojcieszek, Stephanie Antonopoulos, Ji In Kim, Jane S. Paulsen, Maryjane Ong, Spencer Lourens, Maria Tedesco, Katrin Barth, Christina Reeves, Jane Griffith, Peter K. Panegyres, Sarah Hunt, Cathy Wood-Siverio, David Craufurd, Holly James Westervelt, Zosia Miedzybrodzka, A. Coleman, Irita Karmalkar, Joseph W. Y. Lee, Carolin Eschenbach, Greg Suter, Christopher A. Ross, Satwinder Sran, Sharon J. Sha, Daniela Schwenk, Joel S. Perlmutter, Ali Samii, James A. Mills, Mark Varvaris, Amanda Miller, Frederick J. Marshall, Amy M. Chesire, Isabella De Soriano, Ying Zhang, Natalie Valle Guzman, Angela Komiti, Oksana Suchowersky, Clement T. Loy, Diane Erickson, Karen Marder, Lyla Mourany, Joseph Winer, Anwar Ahmed, Jatin G. Vaidya, Eun Young Kim, Stacey K. Barton, Cheryl Erwin, Sonja Trautmann, Amanda Martin, Stewart A. Factor, Elizabeth McCusker, Mariella D'Alessandro, Jeffrey D. Long, Randi Jones, Nancy R. Downing, Jared M. Bruce, Charlyne Hickey, Rajeev Kumar, Mannie Fan, Sarah E Tomaszewski Farias
Publikováno v:
J Clin Exp Neuropsychol
Huntington disease (HD) is a neurodegenerative condition with prominent motor (including oculomotor), cognitive, and psychiatric effects. While neuropsychological deficits are present in HD, motor impairments may impact performance on neuropsychologi
Autor:
Michael K. McCormack, Susan Perlman, Julie C. Stout, Nicholas R. Boileau, Joel S. Perlmutter, Nora E. Fritz, Kimberly A. Quaid, Rebecca E. Ready, Jane S. Paulsen, Noelle E. Carlozzi, Stacey K. Barton
Up to 90% of individuals with Huntington's disease (HD)-a progressive, inherited neurodegenerative disorder-experience apathy. Apathy is particularly debilitating because it is marked by a reduction in goal-directed behaviors, including self-care, so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ae812c3fc602057d3d07c87705c4fb8
https://europepmc.org/articles/PMC6081241/
https://europepmc.org/articles/PMC6081241/
Autor:
Michael Wasserman, Monique M. Williams, Helen Hochstetler, Michael J. Pontecorvo, Kimberly A. Quaid, Gail Hunt, Michael M. Witte, James L. Levenson, Gil D. Rabinovici, Luann E. Van Campen, Adam S. Fleisher, Norman L. Foster, J. Scott Roberts, Paula T. Trzepacz, Linda B. Tabas, Ann Marie Hake, Craig A. Hunter
Publikováno v:
Alzheimer's & Dementia : Diagnosis, Assessment & Disease Monitoring
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 1, Iss 3, Pp 358-367 (2015)
Alzheimer's & dementia (Amsterdam, Netherlands), vol 1, iss 3
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 1, Iss 3, Pp 358-367 (2015)
Alzheimer's & dementia (Amsterdam, Netherlands), vol 1, iss 3
Until recently, estimation of β‐amyloid plaque density as a key element for identifying Alzheimer's disease (AD) pathology as the cause of cognitive impairment was only possible at autopsy. Now with amyloid‐positron emission tomography (amyloid
Autor:
Robert Cook-Deegan, Thomas O. Obisesan, Grace Ann Fasaye, T. Obisesan, E. McCarty Wood, Susie A. Sami, Lan Q. Le, Eric J. Topol, S. Hiraki, Debra L. Roter, L. Wright, Robert C. Green, Elana Cox, Eric T. Juengst, Megan S. Johnson, Norman R. Relkin, Patrick Griffith, Kristin Harkins, A D Sadovnick, Stephanie Johnson, Elana Levinson, Leo B. Waterston, Erin Linnenbringer, Pamela Sankar, Stephen G. Post, Jason Karlawish, Melissa Barber Butson, Charmaine D.M. Royal, Lisa D. Ravdin, Chen Chen, Kurt D. Christensen, Kimberly A. Quaid, Deepak L. Bhatt, Lindsay A. Farrer, Deborah Blacker, J. Scott Roberts, L. Adrienne Cupples, Peter J. Whitehouse, Jessica G. Davis, Wendy R. Uhlmann, Barbara B. Biesecker, Robert S. Stern
Publikováno v:
Alzheimer's & Dementia. 11:1222-1230
Conventional multisession genetic counseling is currently recommended when disclosing apolipoprotein E (APOE) genotype for the risk of Alzheimer's disease (AD) in cognitively normal individuals. The objective of this study was to evaluate the safety