Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maria C, Tartaglia"'
Autor:
Daniela Andriuta, Joel Ramirez, Fuqiang Gao, Jennifer Rabin, Madeline E Wood, Paula M McLaughlin, Christopher JM Scott, Miracle Ozzoude, Allison A Dilliott, Robert A Hegele, Maria C Tartaglia, David Tang-Wai, Richard H Swartz, Leanne Casaubon, Sanjeev Kumar, Dar Dowlatshahi, Jennifer Mandzia, Demetrios Sahlas, Gustavo Saposnik, Corinne Fischer, Michael Borrie, Ayman Hassan, Malcolm A Binns, Morris Freedman, Elizabeth Finger, Andrew Frank, Robert Bartha, Sean Symons, Mario Masellis, Sandra E Black
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 6, Iss , Pp 100292- (2024)
Introduction: MRI-visible perivascular spaces (PVS) are a neuroimaging feature of cerebral small vessel disease and are commonly observed in patients with cerebrovascular and neurodegenerative disease. However, it is unclear whether PVS burden is ass
Externí odkaz:
https://doaj.org/article/3072b8b20a2542edba402451a620a4f6
Autor:
Erin Gibson, Joel Ramirez, Lauren A. Woods, Rosa Sommers, Nasim M. Ghahjaverestan, Christopher J.M. Scott, Fuqiang Gao, Anthony E. Lang, Connie Marras, David P. Breen, Maria C. Tartaglia, Malcolm A. Binns, Robert Bartha, Sean Symons, Richard H. Swartz, Mario Masellis, Sandra E. Black, Alan Moody, Andrew SP Lim, Maged Goubran
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 6, Iss , Pp 100305- (2024)
Introduction: White matter hyperintensities (WMH) and MRI-visible perivascular spaces (PVS) are neuroimaging features of cerebral small vessel disease (CSVD). PVS are believed to play a role in cerebral metabolic waste clearance, particularly during
Externí odkaz:
https://doaj.org/article/a3f39586cc584821809ea747ab2a8349
Autor:
Joel Ramirez, Kirstin Walker, Melissa McSweeney, Hassan Akhavein, Melissa F. Holmes, Miracle Ozzoude, Christopher JM Scott, Fuqiang Gao, Seyyed MH Haddad, Paula McLaughlin, Brian Levine, Donna Kwan, Manuel Montero-Odasso, Elizabeth Finger, William E McIlroy, Anthony E. Lang, Maria C. Tartaglia, Jennifer Mandzia, Bradley J MacIntosh, Morris Freedman, Jennifer Rabin, Stephen C. Strother, Mario Masellis, Sean Symons, Robert Bartha, Andrew Lim, Richard H Swartz, Sandra E Black, Maged Goubran
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 6, Iss , Pp 100097- (2024)
Externí odkaz:
https://doaj.org/article/810b7aad2a7f4d9eb3c73a1afc6b7a82
Autor:
Saurabh Sihag, Sébastien Naze, Foad Taghdiri, Melisa Gumus, Charles Tator, Robin Green, Brenda Colella, Kaj Blennow, Henrik Zetterberg, Luis Garcia Dominguez, Richard Wennberg, David J. Mikulis, Maria C. Tartaglia, James R. Kozloski
Publikováno v:
Communications Medicine, Vol 2, Iss 1, Pp 1-14 (2022)
Sihag et al. analyse brain imaging data, circulating neurofilament light chain levels and personality scores in a cohort of former athletes with a history of concussions. The authors use graph signal processing to identify brain structural and connec
Externí odkaz:
https://doaj.org/article/76b22a0035f340ca81f0b11054dc2e46
Autor:
Allison A. Dilliott, Abdalla Abdelhady, Kelly M. Sunderland, Sali M. K. Farhan, Agessandro Abrahao, Malcolm A. Binns, Sandra E. Black, Michael Borrie, Leanne K. Casaubon, Dar Dowlatshahi, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, Morris Freedman, David Grimes, Ayman Hassan, Mandar Jog, Sanjeev Kumar, Donna Kwan, Anthony E. Lang, Jennifer Mandzia, Mario Masellis, Adam D. McIntyre, Stephen H. Pasternak, Bruce G. Pollock, Tarek K. Rajji, Ekaterina Rogaeva, Demetrios J. Sahlas, Gustavo Saposnik, Christine Sato, Dallas Seitz, Christen Shoesmith, Thomas D. L. Steeves, Richard H. Swartz, Brian Tan, David F. Tang-Wai, Maria C. Tartaglia, John Turnbull, Lorne Zinman, ONDRI Investigators, Robert A. Hegele
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
Abstract Genetic factors contribute to neurodegenerative diseases, with high heritability estimates across diagnoses; however, a large portion of the genetic influence remains poorly understood. Many previous studies have attempted to fill the gaps b
Externí odkaz:
https://doaj.org/article/c14898e55b0f4ab5b45663002d305766
Autor:
Allison A. Dilliott, Kristina K. Zhang, Jian Wang, Agessandro Abrahao, Malcolm A. Binns, Sandra E. Black, Michael Borrie, Dar Dowlatshahi, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, Morris Freedman, David Grimes, Ayman Hassan, Mandar Jog, Sanjeev Kumar, Anthony E. Lang, Jennifer Mandzia, Mario Masellis, Stephen H. Pasternak, Bruce G. Pollock, Tarek K. Rajji, Ekaterina Rogaeva, Demetrios J. Sahlas, Gustavo Saposnik, Christine Sato, Dallas Seitz, Christen Shoesmith, Thomas D. L. Steeves, Richard H. Swartz, Brian Tan, David F. Tang‐Wai, Maria C. Tartaglia, John Turnbull, Lorne Zinman, ONDRI Investigators, Robert A. Hegele
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background Although genetic factors are known to contribute to neurodegenerative disease susceptibility, there remains a large amount of heritability unaccounted for across the diagnoses. Copy number variants (CNVs) contribute to these pheno
Externí odkaz:
https://doaj.org/article/649dad53d67b47c99ebb458bbdb9833e
Autor:
Miracle Ozzoude, Joel Ramirez, Pradeep Reddy Raamana, Melissa F. Holmes, Kirstin Walker, Christopher J. M. Scott, Fuqiang Gao, Maged Goubran, Donna Kwan, Maria C. Tartaglia, Derek Beaton, Gustavo Saposnik, Ayman Hassan, Jane Lawrence-Dewar, Dariush Dowlatshahi, Stephen C. Strother, Sean Symons, Robert Bartha, Richard H. Swartz, Sandra E. Black
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
BackgroundRegional changes to cortical thickness in individuals with neurodegenerative and cerebrovascular diseases (CVD) can be estimated using specialized neuroimaging software. However, the presence of cerebral small vessel disease, focal atrophy,
Externí odkaz:
https://doaj.org/article/ff5a98fd84e94b8d8bc7362cf0c7bc27
Autor:
Anna Vasilevskaya, Foad Taghdiri, Namita Multani, Cassandra Anor, Karen Misquitta, Sylvain Houle, Charles Burke, David Tang-Wai, Anthony E. Lang, Susan Fox, Elizabeth Slow, Pablo Rusjan, Maria C. Tartaglia
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Introduction: Frontotemporal lobar degeneration (FTLD)-related syndrome includes progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS). PSP is usually caused by a tauopathy but can have associated Alzheimer's disease (AD) while CBS can
Externí odkaz:
https://doaj.org/article/03f39dc79a1a4ac2a596bcceae31add9
Autor:
Anna Vasilevskaya, Foad Taghdiri, Charles Burke, Apameh Tarazi, Seyed Ali Naeimi, Mozghan Khodadadi, Ruma Goswami, Christine Sato, Mark Grinberg, Danielle Moreno, Richard Wennberg, David Mikulis, Robin Green, Brenda Colella, Karen D. Davis, Pablo Rusjan, Sylvain Houle, Charles Tator, Ekaterina Rogaeva, Maria C. Tartaglia
Publikováno v:
NeuroImage: Clinical, Vol 26, Iss , Pp - (2020)
Background: Genetic polymorphisms like apolipoprotein E (APOE) and microtubule-associated protein tau (MAPT) genes increase the risk of neurodegeneration. Methods: 38 former players (age 52.63±14.02) of contact sports underwent neuroimaging, bioflui
Externí odkaz:
https://doaj.org/article/67247a18e77f4fbfad0c0566d25c64e3
Autor:
Giorgio G. Fumagalli, Paola Basilico, Andrea Arighi, Martina Bocchetta, Katrina M. Dick, David M. Cash, Sophie Harding, Matteo Mercurio, Chiara Fenoglio, Anna M. Pietroboni, Laura Ghezzi, John van Swieten, Barbara Borroni, Alexandre de Mendonça, Mario Masellis, Maria C. Tartaglia, James B. Rowe, Caroline Graff, Fabrizio Tagliavini, Giovanni B. Frisoni, Robert Laforce, Elizabeth Finger, Sandro Sorbi, Elio Scarpini, Jonathan D. Rohrer, Daniela Galimberti, on behalf of the Genetic FTD Initiative (GENFI)
Publikováno v:
Alzheimer’s Research & Therapy, Vol 10, Iss 1, Pp 1-9 (2018)
Abstract Background In patients with frontotemporal dementia, it has been shown that brain atrophy occurs earliest in the anterior cingulate, insula and frontal lobes. We used visual rating scales to investigate whether identifying atrophy in these a
Externí odkaz:
https://doaj.org/article/11b92a883e244953bc3d04bc14e476ee