Výsledky vyhledávání - Liisa Myllykangas

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  1. 1
    Aggregated α-Synuclein Mediates Dopaminergic Neurotoxicity<i>In Vivo</i>

    Aggregated α-Synuclein Mediates Dopaminergic Neurotoxicity<i>In Vivo</i> Autor Magali Periquet, Tudor A. Fulga, Liisa Myllykangas, Michael G. Schlossmacher, Mel Β. Feany

    Vydáno 2007
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  2. 2
    Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85+

    Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85+ Autor Anna Raunio, Karri Kaivola, Jarno Tuimala, Mia Kero, Minna Oinas, Tuomo Polvikoski, Anders Paetau, Pentti J. Tienari, Liisa Myllykangas

    Vydáno 2019
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  3. 3
    Neuropathological evidence of body-first vs. brain-first Lewy body disease

    Neuropathological evidence of body-first vs. brain-first Lewy body disease Autor Per Borghammer, Jacob Horsager, Katrine B. Andersen, Nathalie Van Den Berge, Anna Raunio, Shigeo Murayama, Laura Parkkinen, Liisa Myllykangas

    Vydáno 2021
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  4. 4
    <scp>CADASIL</scp> and <scp>CARASIL</scp>

    <scp>CADASIL</scp> and <scp>CARASIL</scp> Autor Saara Tikka, Marc Baumann, Maija Siitonen, Petra Pasanen, Minna Pöyhönen, Liisa Myllykangas, Matti Viitanen, Toshio Fukutake, Emmanuel Cognat, Anne Joutel, Hannu Kalimo

    Vydáno 2014
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  5. 5
    Neuropathologic features of four autopsied COVID‐19 patients

    Neuropathologic features of four autopsied COVID‐19 patients Autor Jonas Kantonen, Shamita Mahzabin, Mikko I. Mäyränpää, Olli Tynninen, Anders Paetau, Noora Andersson, Antti Sajantila, Olli Vapalahti, Olli Carpén, Eliisa Kekäläinen, Anu Kantele, Liisa Myllykangas

    Vydáno 2020
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  6. 6
    A postmortem study suggests a revision of the dual-hit hypothesis of Parkinson’s disease

    A postmortem study suggests a revision of the dual-hit hypothesis of Parkinson’s disease Autor Per Borghammer, Mie Kristine Just, Jacob Horsager, Casper Skjærbæk, Anna Raunio, Eloise Kok, Sara Savola, Shigeo Murayama, Yuko Saito, Liisa Myllykangas, Nathalie Van Den Berge

    Vydáno 2022
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  7. 7
    Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo

    Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo Autor Valerie Cullen, Maria Lindfors, Juliana Ng, Anders Paetau, Erika Swinton, Piotr Kolodziej, Heather Boston, Paul Säftig, John Woulfe, Mel Β. Feany, Liisa Myllykangas, Michael G. Schlossmacher, Jaana Tyynelä

    Vydáno 2009
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  8. 8
    Plasma homocysteine, Alzheimer and cerebrovascular pathology: a population-based autopsy study

    Plasma homocysteine, Alzheimer and cerebrovascular pathology: a population-based autopsy study Autor Babak Hooshmand, Tuomo Polvikoski, Miia Kivipelto, Maarit Tanskanen, Liisa Myllykangas, Timo Erkinjuntti, Mira Mäkelä, Minna Oinas, Anders Paetau, Philip Scheltens, Elisabeth C.W. van Straaten, Raimo Sulkava, Alina Solomon

    Vydáno 2013
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  9. 9
    Prediction models for dementia and neuropathology in the oldest old: the Vantaa 85+ cohort study

    Prediction models for dementia and neuropathology in the oldest old: the Vantaa 85+ cohort study Autor Anette Hall, Timo Pekkala, Tuomo Polvikoski, Mark van Gils, Miia Kivipelto, Jyrki Lötjönen, Jussi Mattila, Mia Kero, Liisa Myllykangas, Mira Mäkelä, Minna Oinas, Anders Paetau, Hilkka Soininen, Maarit Tanskanen, Alina Solomon

    Vydáno 2019
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  10. 10
    Novel mutations consolidate<i>KCTD7</i>as a progressive myoclonus epilepsy gene

    Novel mutations consolidate<i>KCTD7</i>as a progressive myoclonus epilepsy gene Autor Maria Kousi, Verneri Anttila, Angela Schulz, Stella Calafato, Eveliina Jakkula, Erik Riesch, Liisa Myllykangas, Hannu Kalimo, Meral Topçu, Sarenur Gökben, Füsun Alehan, Johannes R. Lemke, Michael Alber, Aarno Palotie, Outi Kopra, Anna‐Elina Lehesjoki

    Vydáno 2012
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  11. 11
    Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

    Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study Autor Hannu Laaksovirta, Terhi Peuralinna, Jennifer C. Schymick, Sonja W. Scholz, Shaoi-Lin Lai, Liisa Myllykangas, Raimo Sulkava, Lilja Jansson, Dena Hernández, J. Raphael Gibbs, Michael A. Nalls, David Heckerman, Pentti J. Tienari, Bryan J. Traynor

    Vydáno 2010
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  12. 12
    APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study

    APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study Autor Samu Kurki, Jonas Kantonen, Karri Kaivola, Laura Hokkanen, Mikko I. Mäyränpää, Henri Puttonen, Juha Martola, Minna Pöyhönen, Mia Kero, Jarno Tuimala, Olli Carpén, Anu Kantele, Olli Vapalahti, Marjaana Tiainen, Pentti J. Tienari, Kai Kaila, Johanna Hästbacka, Liisa Myllykangas

    Vydáno 2021
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  13. 13
    The chromosome 9 ALS and FTD locus is probably derived from a single founder

    The chromosome 9 ALS and FTD locus is probably derived from a single founder Autor Kin Y. Mok, Bryan J. Traynor, Jennifer C. Schymick, Pentti J. Tienari, Hannu Laaksovirta, Terhi Peuralinna, Liisa Myllykangas, Adriano Chió, Aleksey Shatunov, Bradley F. Boeve, Adam L. Boxer, Mariely DeJesus‐Hernandez, Ian R. Mackenzie, Adrian J. Waite, Nigel Williams, Huw R. Morris, Javier Simón‐Sánchez, John C. van Swieten, Peter Heutink, Gabriella Restagno, Gabriele Mora, Karen Morrison, Pamela J. Shaw, Pamela Sara Rollinson, Ammar Al‐Chalabi, Rosa Rademakers, Stuart Pickering‐Brown, Richard W. Orrell, Michael A. Nalls, John Hardy

    Vydáno 2011
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  14. 14
    Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy

    Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy Autor Ellen Gelpí, Raphael Reinecke, Carles Gaig, Àlex Iranzo, Lídia Sabater, Laura Molina‐Porcel, Ibán Aldecoa, Verena Endmayr, Birgit Högl, Erich Schmutzhard, Werner Poewe, Bettina Pfausler, Mara Popović, Janja Pretnar Oblak, Frank Leypoldt, Jakob Matschke, Markus Glatzel, Elena Erro, Ivonne Jericó, María Cristina Caballero, María Victoria Zelaya, Sara Mariotto, Anna Heidbreder, Ognian Kalev, Serge Weis, Stefan Macher, Evelyn Berger–Sieczkowski, Julia Ferrari, Christoph Reisinger, Nikolaus Klupp, Pentti Tienari, Osma S. Rautila, Miska Aleksanteri Niemelä, Deniz Yilmazer‐Hanke, Mar Guasp, Bas R. Bloem, Judith Van Gaalen, Benno Küsters, Maarten J. Titulaer, Nina L. Fransen, Joan Santamaría, Timothy Dawson, Janice L. Holton, Helen Ling, Tamás Révész, Liisa Myllykangas, Herbert Budka, Gábor G. Kovács, Jan Lewerenz, Josep Dalmau, Francesc Graus, Inga Koneczny, Romana Höftberger

    Vydáno 2024
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  15. 15
    Frequency of LATE neuropathologic change across the spectrum of Alzheimer’s disease neuropathology: combined data from 13 community-based or population-based autopsy cohorts

    Frequency of LATE neuropathologic change across the spectrum of Alzheimer’s disease neuropathology: combined data from 13 community-based or population-based autopsy cohorts Autor Peter T. Nelson, Carol Brayne, Margaret E. Flanagan, Erin L. Abner, Sonal Agrawal, Johannes Attems, Rudolph J. Castellani, María M. Corrada, Matthew D. Cykowski, Jing Di, Dennis W. Dickson, Brittany N. Dugger, John F. Ervin, Jane Fleming, Jonathan Graff‐Radford, Lea T. Grinberg, Suvi R. K. Hokkanen, Sally Hunter, Alifiya Kapasi, Claudia H. Kawas, Hannah A. D. Keage, C. Dirk Keene, Mia Kero, David S. Knopman, Naomi Kouri, Gábor G. Kovács, Sydney A. Labuzan, Eric B. Larson, Caitlin S. Latimer, Renata Elaine Paraízo Leite, Billie J. Matchett, Fiona E. Matthews, Richard L. Merrick, Thomas J. Montine, Melissa E. Murray, Liisa Myllykangas, Sukriti Nag, Ruth S. Nelson, Janna H. Neltner, Aivi T. Nguyen, Ronald C. Petersen, Tuomo Polvikoski, R. Ross Reichard, Roberta Diehl Rodriguez, Cláudia Kimie Suemoto, Shih‐Hsiu J. Wang, Stephen B. Wharton, Lon R. White, Julie A. Schneider

    Vydáno 2022
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  16. 16
    LATE-NC staging in routine neuropathologic diagnosis: an update

    LATE-NC staging in routine neuropathologic diagnosis: an update Autor Peter T. Nelson, Edward B. Lee, Matthew D. Cykowski, Irina Alafuzoff, Konstantinos Arfanakis, Johannes Attems, Carol Brayne, María M. Corrada, Brittany N. Dugger, Margaret E. Flanagan, Bernardino Ghetti, Lea T. Grinberg, Murray Grossman, Michel J. Grothe, Glenda M. Halliday, Masato Hasegawa, Suvi R. K. Hokkanen, Sally Hunter, K. A. Jellinger, Claudia H. Kawas, C. Dirk Keene, Naomi Kouri, Gábor G. Kovács, James B. Leverenz, Caitlin S. Latimer, Ian R. Mackenzie, Qinwen Mao, Kirsty E. McAleese, Richard L. Merrick, Thomas J. Montine, Melissa E. Murray, Liisa Myllykangas, Sukriti Nag, Janna H. Neltner, Kathy L. Newell, Robert A. Rissman, Yuko Saito, S. Ahmad Sajjadi, Katherine E. Schwetye, Andrew F. Teich, Dietmar Rudolf Thal, Sandra O. Tomé, Juan C. Troncoso, Shih‐Hsiu J. Wang, Charles L. White, Thomas Wısnıewskı, Hyun‐Sik Yang, Julie A. Schneider, Dennis W. Dickson, Manuela Neumann

    Vydáno 2022
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  17. 17
    Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

    Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study Autor Rita Guerreiro, Owen A. Ross, Célia Kun‐Rodrigues, Dena Hernández, Tatiana Orme, John D. Eicher, Claire E. Shepherd, Laura Parkkinen, Lee Darwent, Michael G. Heckman, Sonja W. Scholz, Juan C. Troncoso, Olga Pletnikova, Olaf Ansorge, Jordi Clarimón, Alberto Lleó, Estrella Morenas‐Rodríguez, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Afina W. Lemstra, Ekaterina Rogaeva, Peter St George‐Hyslop, Elisabet Londos, Henrik Zetterberg, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Janice L. Holton, Yaroslau Compta, Vivianna M. Van Deerlin, Geidy E. Serrano, Thomas G. Beach, Suzanne Lesage, Douglas Galasko, Eliezer Masliah, Isabel Santana, Pau Pástor, Mónica Díez-Fairén, Miquel Aguilar, Pentti J. Tienari, Liisa Myllykangas, Minna Oinas, Tamás Révész, Andrew J. Lees, Bradley F. Boeve, Ronald C. Petersen, Tanis J. Ferman, Valentina Escott‐Price, Caroline Graff, Nigel J. Cairns, John C. Morris, Stuart Pickering‐Brown, David Mann, Glenda M. Halliday, John Hardy, John Q. Trojanowski, Dennis W. Dickson, Andrew Singleton, David J. Stone, José Brás

    Vydáno 2017
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  18. 18
    A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

    A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD Autor Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson, J. Raphael Gibbs, Jennifer C. Schymick, Hannu Laaksovirta, John C. van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M. Remes, Alice Kaganovich, Sonja W. Scholz, Jamie Duckworth, Jinhui Ding, Daniel W. Harmer, Dena G. Hernandez, Janel O. Johnson, Kin Y. Mok, Mina Ryten, Daniah Trabzuni, Rita Guerreiro, Richard W. Orrell, James Neal, Alex Murray, Justin Pearson, Iris E. Jansen, David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chió, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor

    Vydáno 2011
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  19. 19
    Heritability and genetic variance of dementia with Lewy bodies

    Heritability and genetic variance of dementia with Lewy bodies Autor Rita Guerreiro, Valentina Escott‐Price, Dena Hernandez, Célia Kun‐Rodrigues, Owen A. Ross, Tatiana Orme, João Luís Neto, Susana Carmona, Nadia Dehghani, John D. Eicher, Claire E. Shepherd, Laura Parkkinen, Lee Darwent, Michael G. Heckman, Sonja W. Scholz, Juan C. Troncoso, Olga Pletnikova, Ted M. Dawson, Liana S. Rosenthal, Olaf Ansorge, Jordi Clarimón, Alberto Lleó, Estrella Morenas‐Rodríguez, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Afina W. Lemstra, Ekaterina Rogaeva, Peter St George–Hyslop, Elisabet Londos, Henrik Zetterberg, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Janice L. Holton, Yaroslau Compta, Vivianna M. Van Deerlin, Geidy E. Serrano, Thomas G. Beach, Suzanne Lesage, Douglas Galasko, Eliezer Masliah, Isabel Santana, Pau Pástor, Mónica Díez-Fairén, Miquel Aguilar, Pentti J. Tienari, Liisa Myllykangas, Minna Oinas, Tamás Révész, Andrew J. Lees, Bradley F. Boeve, Ronald C. Petersen, Tanis J. Ferman, Caroline Graff, Nigel J. Cairns, John C. Morris, Stuart Pickering‐Brown, David Mann, Glenda M. Halliday, John Hardy, John Q. Trojanowski, Dennis W. Dickson, Andrew Singleton, David J. Stone, José Brás

    Vydáno 2019
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  20. 20
    Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

    Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture Autor Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Regina H. Reynolds, Emil K. Gustavsson, Ronald L. Walton, Sarah Ahmed, Coralie Viollet, Jinhui Ding, Mary B. Makarious, Mónica Díez-Fairén, Makayla K. Portley, Zalak Shah, Yevgeniya Abramzon, Dena Hernández, Cornelis Blauwendraat, David J. Stone, John D. Eicher, Laura Parkkinen, Olaf Ansorge, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Afina W. Lemstra, Peter St George‐Hyslop, Elisabet Londos, Kevin Morgan, Tammaryn Lashley, Thomas T. Warner, Zane Jaunmuktane, Douglas Galasko, Isabel Santana, Pentti J. Tienari, Liisa Myllykangas, Minna Oinas, Nigel J. Cairns, John C. Morris, Glenda M. Halliday, Vivianna M. Van Deerlin, John Q. Trojanowski, Maurizio Grassano, Andrea Calvo, Gabriele Mora, Antonio Canosa, Gianluca Floris, Ryan C. Bohannan, Francesca Brett, Ziv Gan‐Or, Joshua T. Geiger, Anni Moore, Patrick May, Rejko Krüger, David S. Goldstein, Grisel Lopez, Nahid Tayebi, Ellen Sidransky, Anthony R. Sotis, Gauthaman Sukumar, Camille Alba, Nathaniel M. Lott, Elisa McGrath Martinez, Meila Tuck, Jatinder Singh, Dagmar Bačíková, Xijun Zhang, Daniel Hupalo, Adelani Adeleye, Matthew D. Wilkerson, Harvey B. Pollard, Lucy Norcliffe‐Kaufmann, Jose‐Alberto Palma, Horacio Kaufmann, Vikram G. Shakkottai, Matthew Perkins, Kathy L. Newell, Thomas Gasser, Claudia Schulte, Francesco Landi, Erika Salvi, Daniele Cusi, Eliezer Masliah, Ronald C. Kim, Chad A. Caraway, Edwin S. Monuki, Maura Brunetti, Ted M. Dawson, Liana S. Rosenthal, Marilyn S. Albert, Olga Pletnikova, Juan C. Troncoso, Margaret E. Flanagan, Qinwen Mao, Eileen H. Bigio, Eloy Rodríguez‐Rodríguez, Jon Infante, Carmen Lage, Isabel González Aramburu, Pascual Sánchez‐Juan, Bernardino Ghetti

    Vydáno 2021
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