Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Shanu F Roemer"'
Autor:
Nobutaka Sakae, Shanu F. Roemer, Kevin F. Bieniek, Melissa E. Murray, Matthew C. Baker, Koji Kasanuki, Neill R. Graff‐Radford, Leonard Petrucelli, Marka Van Blitterswijk, Rosa Rademakers, Dennis W. Dickson
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 9, Pp 1782-1796 (2019)
Abstract Objective To identify clinicopathological differences between frontotemporal lobar degeneration (FTLD) due to mutations in progranulin (FTLD‐GRN) and chromosome 9 open reading frame 72 (FTLD‐C9ORF72). Methods We performed quantitative ne
Externí odkaz:
https://doaj.org/article/7f413b148bef45bca5c50915fd71e1b1
Autor:
Rebecca R Valentino, William J Scotton, Shanu F Roemer, Tammaryn Lashley, Michael G Heckman, Maryam Shoai, Alejandro Martinez-Carrasco, Nicole Tamvaka, Ronald L Walton, Matthew C Baker, Hannah L Macpherson, Raquel Real, Alexandra I Soto-Beasley, Kin Mok, Tamas Revesz, Thomas T Warner, Zane Jaunmuktane, Bradley F Boeve, Elizabeth A Christopher, Michael DeTure, Ranjan Duara, Neill R Graff-Radford, Keith A Josephs, David S Knopman, Shunsuke Koga, Melissa E Murray, Kelly E Lyons, Rajesh Pahwa, Joseph E Parisi, Ronald C Petersen, Jennifer Whitwell, Lea T Grinberg, Bruce Miller, Athena Schlereth, William W Seeley, Salvatore Spina, Murray Grossman, David J Irwin, Edward B Lee, EunRan Suh, John Q Trojanowski, Vivianna M Van Deerlin, David A Wolk, Theresa R Connors, Patrick M Dooley, Matthew P Frosch, Derek H Oakley, Iban Aldecoa, Mircea Balasa, Ellen Gelpi, Sergi Borrego-Écija, Rosa Maria de Eugenio Huélamo, Jordi Gascon-Bayarri, Raquel Sánchez-Valle, Pilar Sanz-Cartagena, Gerard Piñol-Ripoll, Laura Molina-Porcel, Eileen H Bigio, Margaret E Flanagan, Tamar Gefen, Emily J Rogalski, Sandra Weintraub, Javier Redding-Ochoa, Koping Chang, Juan C Troncoso, Stefan Prokop, Kathy L Newell, Bernardino Ghetti, Matthew Jones, Anna Richardson, Andrew C Robinson, Federico Roncaroli, Julie Snowden, Kieren Allinson, Oliver Green, James B Rowe, Poonam Singh, Thomas G Beach, Geidy E Serrano, Xena E Flowers, James E Goldman, Allison C Heaps, Sandra P Leskinen, Andrew F Teich, Sandra E Black, Julia L Keith, Mario Masellis, Istvan Bodi, Andrew King, Safa-Al Sarraj, Claire Troakes, Glenda M Halliday, John R Hodges, Jillian J Kril, John B Kwok, Olivier Piguet, Marla Gearing, Thomas Arzberger, Sigrun Roeber, Johannes Attems, Christopher M Morris, Alan J Thomas, Bret M. Evers, Charles L White, Naguib Mechawar, Anne A Sieben, Patrick P Cras, Bart B De Vil, Peter Paul P.P. De Deyn, Charles Duyckaerts, Isabelle Le Ber, Danielle Seihean, Sabrina Turbant-Leclere, Ian R MacKenzie, Catriona McLean, Matthew D Cykowski, John F Ervin, Shih-Hsiu J Wang, Caroline Graff, Inger Nennesmo, Rashed M Nagra, James Riehl, Gabor G Kovacs, Giorgio Giaccone, Benedetta Nacmias, Manuela Neumann, Lee-Cyn Ang, Elizabeth C Finger, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Dan Vitale, Cristina Cunha, Agostinho Carvalho, Zbigniew K Wszolek, Huw R Morris, Rosa Rademakers, John A Hardy, Dennis W Dickson, Jonathan D Rohrer, Owen A Ross
Publikováno v:
medRxiv
BackgroundPick’s disease (PiD) is a rare and predominantly sporadic form of frontotemporal dementia that is classified as a primary tauopathy. PiD is pathologically defined by argyrophilic inclusion Pick bodies and ballooned neurons in the frontal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eb436da4c7362a38f76655e19fddf0a
https://europepmc.org/articles/PMC10168402/
https://europepmc.org/articles/PMC10168402/
Autor:
Gregory S Day, Evelyn Lazar, Nikhil B Ghayal, Shanu F Roemer, Neill R. Graff‐Radford, Dennis W. Dickson
Publikováno v:
Alzheimer's & Dementia. 18
Autor:
Shanu F. Roemer, Lea T. Grinberg, John F. Crary, William W. Seeley, Ann C. McKee, Gabor G. Kovacs, Thomas G. Beach, Charles Duyckaerts, Isidro A. Ferrer, Ellen Gelpi, Edward B. Lee, Tamas Revesz, Charles L. White, Mari Yoshida, Felipe L. Pereira, Kristen Whitney, Nikhil B. Ghayal, Dennis W. Dickson
Publikováno v:
Acta neuropathologica, vol 144, iss 4
Neuropathologic criteria for progressive supranuclear palsy (PSP) proposed by a National Institute of Neurological Disorders and Stroke (NINDS) working group were published in 1994 and based on the presence of neurofibrillary tangles in basal ganglia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eab41220f15886905d446a56640660b
https://escholarship.org/uc/item/6fp5m26k
https://escholarship.org/uc/item/6fp5m26k
Autor:
Shanu F, Roemer, Lea T, Grinberg, John F, Crary, William W, Seeley, Ann C, McKee, Gabor G, Kovacs, Thomas G, Beach, Charles, Duyckaerts, Isidro A, Ferrer, Ellen, Gelpi, Edward B, Lee, Tamas, Revesz, Charles L, White, Mari, Yoshida, Felipe L, Pereira, Kristen, Whitney, Nikhil B, Ghayal, Dennis W, Dickson
Publikováno v:
Acta neuropathologica. 144(4)
Neuropathologic criteria for progressive supranuclear palsy (PSP) proposed by a National Institute of Neurological Disorders and Stroke (NINDS) working group were published in 1994 and based on the presence of neurofibrillary tangles in basal ganglia
Autor:
Na Zhao, Anna I. Wernick, Shanu F. Roemer, Ronald L. Walton, Dennis W. Dickson, William P. Cheshire, Owen A. Ross, Neill R. Graff-Radford, Ayman H. Faroqi, Shunsuke Koga, Fuyao Li, Tanis J. Ferman
Publikováno v:
Brain Pathology (Zurich, Switzerland)
Background: Abnormal aggregates of α‐synuclein are pathologic hallmarks of multiple system atrophy (MSA) and Lewy body disease (LBD). LBD sometimes coexists with MSA, but the impact of co‐pathology, particularly diffuse LBD, on presentation of M
Publikováno v:
Parkinsonism Relat Disord
Background The corticobasal syndrome (CBS) is heterogeneous in terms of postmortem neuropathology. While it has been previously studied with antemortem neuroimaging, clinicopathologic features of corticobasal syndrome associated with cerebrovascular
Autor:
Neill R. Graff-Radford, Kevin F. Bieniek, Nobutaka Sakae, Matt Baker, Koji Kasanuki, Marka van Blitterswijk, Melissa E. Murray, Leonard Petrucelli, Dennis W. Dickson, Rosa Rademakers, Shanu F. Roemer
Publikováno v:
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 6, Iss 9, Pp 1782-1796 (2019)
Annals of Clinical and Translational Neurology, Vol 6, Iss 9, Pp 1782-1796 (2019)
Objective To identify clinicopathological differences between frontotemporal lobar degeneration (FTLD) due to mutations in progranulin (FTLD-GRN) and chromosome 9 open reading frame 72 (FTLD-C9ORF72). Methods We performed quantitative neuropathologic
Autor:
Rosa Rademakers, J. Eric Ahlskog, Owen A. Ross, Shunsuke Koga, Shanu F. Roemer, Takuya Konno, Michael DeTure, Dennis W. Dickson, Matt Baker
Publikováno v:
J Neuropathol Exp Neurol
Progressive supranuclear palsy with predominant cerebellar ataxia (PSP-C) has been reported as a rare clinical subtype, but the underlying pathology of its cerebellar ataxia remains unclear. Here, we report a patient with the coexistence of PSP with
Autor:
John D. Fryer, Matt Baker, Billie J. Matchett, Alexandra M. Nicholson, Wenhui Qiao, Monica Castanedes-Casey, Virginia Phillips, Hung Phuoc Nguyen, Mieu Brooks, Zachary S. Quicksall, Yan W. Asmann, Melissa E. Murray, Shanu F. Roemer, Guojun Bu, Rosa Rademakers, Xiaolai Zhou, Yingxue Ren, Dennis W. Dickson, Ariston L. Librero, Cristhoper H. Fernandez De Castro, Ralph B. Perkerson, Shunsuke Koga, Aishe Kurti
Publikováno v:
Brain Pathology
Brain pathology
Brain pathology
Genetic variants in TMEM106B are a major risk factor for several neurodegenerative diseases including frontotemporal degeneration, limbic-predominant age-related TDP-43 encephalopathy, Parkinson's disease, late-onset-Alzheimer's disease and constitut