Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Denise W. Ng"'
Autor:
Anna E. Blanken, Sona Hurtz, Chris Zarow, Kristina Biado, Hedieh Honarpisheh, Johanne Somme, Jenny Brook, Spencer Tung, Emily Kraft, Darrick Lo, Denise W. Ng, Harry V. Vinters, Liana G. Apostolova
Publikováno v:
NeuroImage: Clinical, Vol 15, Iss , Pp 56-61 (2017)
Hippocampal atrophy, amyloid plaques, and neurofibrillary tangles are established pathologic markers of Alzheimer's disease. We analyzed the temporal lobes of 9 Alzheimer's dementia (AD) and 7 cognitively normal (NC) subjects. Brains were scanned pos
Externí odkaz:
https://doaj.org/article/117a945c54b44e578c567f7c2b11485d
Autor:
Boris C. Bernhardt, Hal Blumenfeld, Yotin Chinvarun, Irene Wang, Denise W. Ng, Fernando Cendes, Stefan Rampp, Victoria L. Morgan, Andrea Bernasconi, Anna Elisabetta Vaudano, Graeme D. Jackson, Paolo Federico
The ILAE Neuroimaging Task Force aims to publish educational case reports highlighting basic aspects related to neuroimaging in epilepsy consistent with the educational mission of the ILAE. It is important to obtain MRI scans early in the clinical co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::700b66791cefc8ba6fc4755fd6575033
https://hdl.handle.net/11380/1268605
https://hdl.handle.net/11380/1268605
Autor:
Hedieh Honarpisheh, Kristina Biado, Anna E. Blanken, Denise W. Ng, Liana G. Apostolova, Jenny Brook, Harry V. Vinters, Emily Kraft, Chris Zarow, Johanne Somme, Darrick Lo, Sona Hurtz, Spencer Tung
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 15, Iss, Pp 56-61 (2017)
NeuroImage: Clinical, Vol 15, Iss, Pp 56-61 (2017)
Hippocampal atrophy, amyloid plaques, and neurofibrillary tangles are established pathologic markers of Alzheimer's disease. We analyzed the temporal lobes of 9 Alzheimer's dementia (AD) and 7 cognitively normal (NC) subjects. Brains were scanned pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b42d05e98f329f9c50e02a6fa5917b2
https://doi.org/10.1016/j.nicl.2017.04.020
https://doi.org/10.1016/j.nicl.2017.04.020
Autor:
Seyed A. Hojat, William H. Yong, Mari Perez-Rosendahl, Timothy F. Cloughesy, Maryam Shabihkhani, Isaac Yang, Albert Lai, Kyuseok Im, Sergey Mareninov, Denise W. Ng, Michael W. Wang, Shino Magaki, Phioanh L. Nghiemphu, Ryan R. Williams, Lawrance K. Chung, Randy S. Tashjian, Harry V. Vinters, Negar Khanlou, Gregory M. Lucey, Bowen Wei, Masoud Movassaghi, Linda M. Liau
Publikováno v:
Experimental and molecular pathology. 103(1)
Background Commercial targeted genomic profiling with next generation sequencing using formalin-fixed paraffin embedded (FFPE) tissue has recently entered into clinical use for diagnosis and for the guiding of therapy. However, there is limited indep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44525fd38c2ffd22ada3c3b0f38bde37
https://pubmed.ncbi.nlm.nih.gov/28663030
https://pubmed.ncbi.nlm.nih.gov/28663030
Autor:
Harry V. Vinters, Kevin H. Terashima, Denise W. Ng, Shino Magaki, Stellios Karnezis, Noriko Salamon, Luke Macyszyn, Adrienne M. Keener
Publikováno v:
Human pathology. 64
Amyloid-β-related angiitis (ABRA) is a rare complication of cerebral amyloid angiopathy in which amyloid-β deposition in the leptomeningeal and cortical vessels is associated with vasculitis characterized by transmural lymphohistiocytic, often gran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::596ace3a548273275937c5ca370f20da
https://pubmed.ncbi.nlm.nih.gov/28161339
https://pubmed.ncbi.nlm.nih.gov/28161339
Autor:
Giovanni Coppola, Yan Zhou, Sandra Weintraub, Amanda Fisher-Hubbard, Mario F. Mendez, Harry V. Vinters, John M. Ringman, Andy Nguyen, Roger L. Albin, Marek-Marsel Mesulam, Darren R. Gitelman, Denise W. Ng, Eileen H. Bigio, Sarah E. Monsell, Victoria Van Berlo, Spencer Tung
Publikováno v:
Journal of neuropathology and experimental neurology. 75(3)
Alzheimer disease (AD) represents a genetically heterogeneous entity. To elucidate neuropathologic features of autosomal dominant AD ([ADAD] due to PSEN1, APP, or PSEN2 mutations), we compared hallmark AD pathologic findings in 60 cases of ADAD and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d218e24cfd029edf2c07338b6bfa11f
https://pubmed.ncbi.nlm.nih.gov/26888304
https://pubmed.ncbi.nlm.nih.gov/26888304
Publikováno v:
American Journal of Clinical Pathology. 138:A050-A050
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f00ab247049ef7f8d1c75766a90cb78
https://doi.org/10.1093/ajcp/138.suppl2.279
https://doi.org/10.1093/ajcp/138.suppl2.279