Risultati della ricerca - Lee-Cyn Ang

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  1. 1
    Neuropathology of Temporal Lobe Epilepsy

    Neuropathology of Temporal Lobe Epilepsy di Fahd Al Sufiani, Lee Cyn Ang

    Pubblicazione 2012
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  2. 2
    Significance of Parkinsonian Manifestations in Essential Tremor

    Significance of Parkinsonian Manifestations in Essential Tremor di A. H. Rajput, B. Rozdilsky, Lee Cyn Ang, Alex Rajput

    Pubblicazione 1993
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  3. 3
    Hospital Nurse Perspectives on Barriers and Facilitators to Caring for Socially Disadvantaged Patients

    Hospital Nurse Perspectives on Barriers and Facilitators to Caring for Socially Disadvantaged Patients di J. Margo Brooks Carthon, K. Jane Muir, Lee Cyn Ang, Kelvin Amenyedor, Daniela Golinelli, Shelli Feder, Ann Kutney‐Lee

    Pubblicazione 2025
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  4. 4
    Versican Enhances Locomotion of Astrocytoma Cells and Reduces Cell Adhesion through Its G1 Domain

    Versican Enhances Locomotion of Astrocytoma Cells and Reduces Cell Adhesion through Its G1 Domain di Lee Cyn Ang, Yaou Zhang, Liu Cao, Bing Yang, Beverley Young, Chris Kiani, Vivian Lee, Katherine S. Allan, Burton B. Yang

    Pubblicazione 1999
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  5. 5
    Low levels of astroglial markers in Parkinson’s disease: relationship to α-synuclein accumulation

    Low levels of astroglial markers in Parkinson’s disease: relationship to α-synuclein accumulation di Junchao Tong, Lee-Cyn Ang, Belinda Williams, Yoshiaki Furukawa, Paul S. Fitzmaurice, Mark Guttman, Isabelle Boileau, Oleh Hornykiewicz, Stephen J. Kish

    Pubblicazione 2015
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  6. 6
    Psychosis and Hallucinations in Frontotemporal Dementia with the C9ORF72 Mutation

    Psychosis and Hallucinations in Frontotemporal Dementia with the C9ORF72 Mutation di Andrew Kertesz, Lee Cyn Ang, Sarah Jesso, Julia MacKinley, Matt Baker, Patricia E. Brown, Christen Shoesmith, Rosa Rademakers, Elizabeth Finger

    Pubblicazione 2013
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  7. 7
    Brain monoamine oxidase B and A in human parkinsonian dopamine deficiency disorders

    Brain monoamine oxidase B and A in human parkinsonian dopamine deficiency disorders di Junchao Tong, Gausiha Rathitharan, Jeffrey H. Meyer, Yoshiaki Furukawa, Lee-Cyn Ang, Isabelle Boileau, Mark Guttman, Oleh Hornykiewicz, Stephen J. Kish

    Pubblicazione 2017
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  8. 8
    Why is parkinsonism not a feature of human methamphetamine users?

    Why is parkinsonism not a feature of human methamphetamine users? di Anna Moszczyńska, Paul S. Fitzmaurice, Lee Cyn Ang, Kathryn S. Kalasinsky, Gregory A. Schmunk, Frank J. Peretti, Sally S. Aiken, Dennis J. Wickham, Stephen J. Kish

    Pubblicazione 2004
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  9. 9
    Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

    Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation di 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

    Pubblicazione 2011
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  10. 10
    MicroRNA miR-93 promotes tumor growth and angiogenesis by targeting integrin-β8

    MicroRNA miR-93 promotes tumor growth and angiogenesis by targeting integrin-β8 di Ling Fang, Zhaoqun Deng, Tatiana Shatseva, Jennifer Yang, Chun Peng, William W. Du, Albert Yee, Lee Cyn Ang, Congfen He, Sze Wan Shan, Burton B. Yang

    Pubblicazione 2010
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  11. 11
    Catheter based selective hypothermia reduces stroke volume during focal cerebral ischemia in swine

    Catheter based selective hypothermia reduces stroke volume during focal cerebral ischemia in swine di 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

    Pubblicazione 2015
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  12. 12
    MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

    MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients di 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

    Pubblicazione 2018
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  13. 13
    FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

    FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations di 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

    Pubblicazione 2011
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  14. 14
    Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity

    Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity di 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

    Pubblicazione 1998
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  15. 15
    MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

    MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study di 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

    Pubblicazione 2024
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