Resultats de la cerca - Lee Cyn Ang
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Neuropathology of Temporal Lobe Epilepsy per Fahd Al Sufiani, Lee Cyn Ang
Publicat 2012Artigo -
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Brain monoamine oxidase B and A in human parkinsonian dopamine deficiency disorders per Junchao Tong, Gausiha Rathitharan, Jeffrey H. Meyer, Yoshiaki Furukawa, Lee-Cyn Ang, Isabelle Boileau, Mark Guttman, Oleh Hornykiewicz, Stephen J. Kish
Publicat 2017Artigo -
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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation per Ian R. Mackenzie, Olaf Ansorge, Michael J. Strong, Juan M. Bilbao, Lorne Zinman, Lee‐Cyn Ang, Matt Baker, Heather Stewart, Andrew Eisen, Rosa Rademakers, Manuela Neumann
Publicat 2011Artigo -
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Catheter based selective hypothermia reduces stroke volume during focal cerebral ischemia in swine per Thomas Mattingly, Lynn Denning, Karen L Siroen, Barb Lehrbass, Pablo López-Ojeda, Larry Stitt, David M. Pelz, Sumit Das, Lee-Cyn Ang, Donald H. Lee, Stephen P. Lownie
Publicat 2015Artigo -
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MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients per Carl O. Olson, Shervin Pejhan, Daniel Kroft, Kimia Sheikholeslami, David Fuss, Marjorie Buist, Annan Ali Sher, Marc R. Del Bigio, Yehezkel Sztainberg, Victoria Mok Siu, Lee Cyn Ang, Marianne Sabourin‐Félix, Tom Moss, Mojgan Rastegar
Publicat 2018Artigo -
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FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations per Manuela Neumann, Eva Bentmann, Dorothee Dormann, Ali Jawaid, Mariely DeJesus‐Hernandez, Olaf Ansorge, Sigrun Roeber, Hans A. Kretzschmar, David G. Muñoz, Hirofumi Kusaka, Osamu Yokota, Lee‐Cyn Ang, Juan M. Bilbao, Rosa Rademakers, Christian Haass, Ian R. Mackenzie
Publicat 2011Artigo -
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Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity per Pedro Piccardo, Stephen R. Dlouhy, Patricia Lievens, Katherine Young, Thomas D. Bird, David Nochlin, Dennis W. Dickson, Harry V. Vinters, Thomas Zimmerman, Ian R. Mackenzie, Stephen J. Kish, Lee‐Cyn Ang, Charles De Carli, Maurizio Pocchiari, Paul Brown, Clarence J. Gibbs, D. C. Gajdusek, Orso Bugiani, James W. Ironside, Fabrizio Tagliavini, Bernardino Ghetti
Publicat 1998Artigo -
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MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study per Rebecca R. Valentino, William J. Scotton, Shanu F. Roemer, Tammaryn Lashley, Michael G. Heckman, Maryam Shoai, Alejandro Martínez-Carrasco, Nicole Tamvaka, Ronald L. Walton, Matthew Baker, Hannah Macpherson, Raquel Real, Alexandra I. Soto‐Beasley, Kin Y. Mok, Tamás Révész, Elizabeth Christopher, Michael DeTure, William W. Seeley, Edward B. Lee, Matthew P. Frosch, Laura Molina‐Porcel, Tamar Gefen, Javier Redding‐Ochoa, Bernardino Ghetti, Andrew Robinson, Christopher Kobylecki, James B. Rowe, Thomas G. Beach, Andrew F. Teich, Julia Keith, István Bódi, Glenda M. Halliday, Marla Gearing, Thomas Arzberger, Christopher M. Morris, Charles L. White, Naguib Mechawar, Susana Boluda, Ian R. Mackenzie, Catriona McLean, Matthew D. Cykowski, Shih‐Hsiu J. Wang, Caroline Graff, Rashed M. Nagra, Gábor G. Kovács, Giorgio Giaccone, Manuela Neumann, Lee-Cyn Ang, Agostinho Carvalho, Huw R. Morris, Rosa Rademakers, John Hardy, Dennis W. Dickson, Jonathan D. Rohrer, Owen A. Ross, Thomas T. Warner, Zane Jaunmuktane, Bradley F. Boeve, Ranjan Duara, Neill R. Graff‐Radford, Keith A. Josephs, David S. Knopman, Shunsuke Koga, Melissa E. Murray, Kelly E. Lyons, Rajesh Pahwa, Ronald Petersen, Jennifer Whitwell, Lea T. Grinberg, Bruce L. Miller, Athena Schlereth, Salvatore Spina, Murray Grossman, David J. Irwin, EunRan Suh, John Q. Trojanowski, Vivianna M. Van Deerlin, David A. Wolk, Theresa R. Connors, Patrick M. Dooley, Derek H. Oakley, Ibán Aldecoa, Mircea Balasa, Ellen Gelpí, Sergi Borrego‐Écija, Jordi Gascón‐Bayarri, Raquel Sánchez‐Valle, Pilar Sanz-Cartagena, Gerard Piñol‐Ripoll, Eileen H. Bigio, Margaret E. Flanagan, Emily Rogalskı, Sandra Weıntraub, Julie A. Schneider, Lihua Peng, Xiongwei Zhu, Koping Chang, Juan C. Troncoso, Stefan Prokop, Kathy L. Newell
Publicat 2024Artigo
Eines de cerca:
Matèries relacionades
Medicine
Biology
Disease
Genetics
Pathology
Gene
Psychology
Dementia
Frontotemporal dementia
Internal medicine
Neuroscience
Amyotrophic lateral sclerosis
Cancer research
Cell biology
Neurodegeneration
Parkinson's disease
Parkinsonism
Psychiatry
Biochemistry
Cell culture
Cytoplasm
Frontotemporal lobar degeneration
Linguistics
Neuropathology
Phenotype
Philosophy
Allele
Alpha-synuclein
Alzheimer's disease
Anesthesia