Resultats de la cerca - Radoslav Matěj
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Biomarkers of Neurodegenerative Diseases: Biology, Taxonomy, Clinical Relevance, and Current Research Status per Dorota Koníčková, Kateřina Menšíková, Lucie Tučková, Eva Hényková, Miroslav Strnad, David Friedecký, David Stejskal, Radoslav Matěj, Petr Kaňovský
Publicat 2022Revisão -
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Neutrophil Extracellular Traps and Thrombolysis Resistance: New Insights for Targeting Therapies per Luca Mengozzi, Ilaria Barison, Martin Malý, Giulia Lorenzoni, Marny Fedrigo, Chiara Castellani, Darío Gregori, Petr Malý, Radoslav Matěj, Petr Toušek, Petr Widimský, Annalisa Angelini
Publicat 2024Artigo -
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A comprehensive immunohistochemical analysis of 26 markers in 250 cases of serous ovarian tumors per Kristýna Němejcová, Adam Šafanda, Michaela Bártů, Romana Michálková, Jana Drozenová, Pavel Fabián, Jitka Hausnerová, Ján Laco, Radoslav Matěj, Gábor Méhes, Petr Škapa, Ivana Stružinská, Pavel Dundr
Publicat 2023Artigo -
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Correlation between p53 immunoexpression and TP53 mutation status in extrapulmonary small cell neuroendocrine carcinomas and its association with patient survival per Klára Pavlíčková, J. Hojný, Petr Waldauf, Pavel Dundr, Nikola Hájková, Marián Švajdler, Pavel Fabián, Iva Staniczková Zambo, Miroslava Flídrová, Ján Laco, Helena Hornychová, Patricie Delongová, Jozef Škarda, Jan Hrudka, Radoslav Matěj
Publicat 2025Artigo -
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Lewy body disease or diseases with Lewy bodies? per Kateřina Menšíková, Radoslav Matěj, Carlo Colosimo, Raymond L. Rosales, Lucie Tučková, Jiří Ehrmann, Dominik Hraboš, Kristýna Kolaříková, Radek Vodička, Radek Vrtěl, Martin Procházka, Martin Nevrlý, Michaela Kaiserová, Sandra Kurčová, Pavel Otruba, Petr Kaňovský
Publicat 2022Revisão -
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Primary Mucinous Tumors of the Ovary: An Interobserver Reproducibility and Detailed Molecular Study Reveals Significant Overlap Between Diagnostic Categories per Pavel Dundr, Michaela Bártů, Tjalling Bosse, Quang Hiep Bui, David Cibula, Jana Drozenová, Pavel Fabián, Oluwole Fadare, Jitka Hausnerová, J. Hojný, Nikola Hájková, Radek Jakša, Ján Laco, Sigurd Lax, Radoslav Matěj, Gábor Méhes, Romana Michálková, Adam Šafanda, Kristýna Němejcová, Naveena Singh, Simona Stolnicu, Marián Švajdler, Tomáš Zima, Ivana Stružinská, W. Glenn McCluggage
Publicat 2023Artigo -
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Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease per Arne De Roeck, Tobi Van den Bossche, Julie van der Zee, Jan Verheijen, Wouter De Coster, Jasper Van Dongen, Lubina Dillen, Yalda Baradaran‐Heravi, Bavo Heeman, Raquel Sánchez‐Valle, Albert Lladó, Benedetta Nacmias, Sandro Sorbi, Ellen Gelpí, Oriol Grau‐Rivera, Estrella Gómez‐Tortosa, Pau Pástor, Sara Ortega‐Cubero, María A. Pastor, Caroline Graff, Håkan Thonberg, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Alexandre de Mendonça, Madalena Martins, Barbara Borroni, Alessandro Padovani, Maria Rosário Almeida, Isabel Santana, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Jordi Clarimón, Alberto Lleó, Juan Fortea, Magda Tsolaki, Maria Koutroumani, Radoslav Matěj, Zdeněk Rohan, Peter Paul De Deyn, Sebastiaan Engelborghs, Patrick Cras, Christine Van Broeckhoven, Kristel Sleegers
Publicat 2017Artigo -
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Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG) per Gábor G. Kovács, Sharon X. Xie, Edward B. Lee, John Robinson, Carrie Caswell, David J. Irwin, Jon B. Toledo, Victoria E. Johnson, Douglas H. Smith, Irina Alafuzoff, Johannes Attems, János Bencze, Kevin F. Bieniek, Eileen H. Bigio, István Bódi, Herbert Budka, Dennis W. Dickson, Brittany N. Dugger, Charles Duyckaerts, Isidró Ferrer, Shelley L. Forrest, Ellen Gelpí, Stephen M. Gentleman, Giorgio Giaccone, Lea T. Grinberg, Glenda M. Halliday, Kimmo J. Hatanpaa, Patrick R. Hof, Monika Hofer, Tibor Hortobágyi, James W. Ironside, Andrew King, Julia Kofler, Enikò Kövari, Jillian J. Kril, Seth Love, Ian R. Mackenzie, Qinwen Mao, Radoslav Matěj, Catriona McLean, David G. Muñoz, Melissa E. Murray, Janna H. Neltner, Peter T. Nelson, Diane Ritchie, Roberta Diehl Rodriguez, Zdeněk Rohan, Annemieke J.M. Rozemüller, Kenji Sakai, Christian Schultz, Danielle Seilhean, Vanessa D. Smith, Paweł Tacik, Hitoshi Takahashi, Takao Masaki, Dietmar Rudolf Thal, Serge Weis, Stephen B. Wharton, Charles L. White, John Woulfe, Masahito Yamada, John Q. Trojanowski
Publicat 2017Artigo -
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Genome-wide association study of autopsy-confirmed Multiple System Atrophy identifies common variants near <i>ZIC1</i> and <i>ZIC4</i> per Franziska Hopfner, Anja Tietz, Viktoria Ruf, Owen A. Ross, Shunsuke Koga, Dennis W. Dickson, Adriano Aguzzi, Johannes Attems, Thomas G. Beach, Allison Beller, Vivianna M. Van Deerlin, Paula Desplats, Günther Deuschl, Charles Duyckaerts, David Ellinghaus, Valentin Evsyukov, Margaret E. Flanagan, André Franke, Matthew P. Frosch, Marla Gearing, Ellen Gelpí, Bernardino Ghetti, Jonathan D. Glass, Lea T. Grinberg, Glenda M. Halliday, Ingo Helbig, Matthias Höllerhage, Inge Huitinga, David J. Irwin, Dirk Keene, Gábor G. Kovács, Edward B. Lee, Johannes Levin, Marı́a José Martı́, Ian R. Mackenzie, Ian G. McKeith, Catriona McLean, Brit Mollenhauer, Manuela Neumann, Kathy L. Newell, Alexander Pantelyat, Manuela Pendziwiat, Annette Peters, Laura Molina‐Porcel, Alberto Rábano, Radoslav Matěj, Alex Rajput, Ali H. Rajput, Regina Reimann, William K. Scott, William W. Seeley, Sashika Selvackadunco, Tanya Simuni, Christine Stadelmann, Per Svenningsson, Alan Thomas, Claudia Trenkwalder, Claire Troakes, John Q. Trojanowski, Charles L. White, Tao Xie, Teresa Ximelis, Justo Yebenes, Ulrich Müller, Daniela Berg, Jochen Herms, Gregor Kuhlenbäumer, Günter U. Höglinger
Publicat 2021Pré-impressão -
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Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy per Gábor G. Kovács, Isidró Ferrer, Lea T. Grinberg, Irina Alafuzoff, Johannes Attems, Herbert Budka, Nigel J. Cairns, John F. Crary, Charles Duyckaerts, Bernardino Ghetti, Glenda M. Halliday, James W. Ironside, Seth Love, Ian R. Mackenzie, David G. Muñoz, Melissa E. Murray, Peter T. Nelson, Hitoshi Takahashi, John Q. Trojanowski, Olaf Ansorge, Thomas Arzberger, Atik Baborie, Thomas G. Beach, Kevin F. Bieniek, Eileen H. Bigio, István Bódi, Brittany N. Dugger, Mel Β. Feany, Ellen Gelpí, Stephen M. Gentleman, Giorgio Giaccone, Kimmo J. Hatanpaa, Richard Heale, Patrick R. Hof, Monika Hofer, Tibor Hortobágyi, K. A. Jellinger, Gregory A. Jicha, Paul G. Ince, Julia Kofler, Enikò Kövari, Jillian J. Kril, David Mann, Radoslav Matěj, Ann C. McKee, Catriona McLean, Ivan Milenković, Thomas J. Montine, Shigeo Murayama, Edward B. Lee, Jasmin Rahimi, Roberta Diehl Rodriguez, Annemieke J.M. Rozemüller, Julie A. Schneider, Christian Schultz, William W. Seeley, Danielle Seilhean, Colin Smith, Fabrizio Tagliavini, Masaki Takao, Dietmar Rudolf Thal, Jon B. Toledo, Markus Tolnay, Juan C. Troncoso, Harry V. Vinters, Serge Weis, Stephen B. Wharton, Charles L. White, Thomas Wısnıewskı, John Woulfe, Masahito Yamada, Dennis W. Dickson
Publicat 2015Revisão -
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Common Variants Near <scp>ZIC1</scp> and <scp>ZIC4</scp> in Autopsy‐Confirmed Multiple System Atrophy per Franziska Hopfner, Anja Tietz, Viktoria Ruf, Owen A. Ross, Shunsuke Koga, Dennis W. Dickson, Adriano Aguzzi, Johannes Attems, Thomas Beach, Allison Beller, William P. Cheshire, Vivianna M. Van Deerlin, Paula Desplats, Günther Deuschl, Charles Duyckaerts, David Ellinghaus, Valentin Evsyukov, Margaret E. Flanagan, André Franke, Matthew P. Frosch, Marla Gearing, Ellen Gelpí, Jay A. van Gerpen, Bernardino Ghetti, Jonathan D. Glass, Lea T. Grinberg, Glenda M. Halliday, Ingo Helbig, Matthias Höllerhage, Inge Huitinga, David J. Irwin, Dirk Keene, Gábor G. Kovács, Edward B. Lee, Johannes Levin, Marı́a José Martı́, Ian R. Mackenzie, Ian G. McKeith, Catriona McLean, Brit Mollenhauer, Manuela Neumann, Kathy L. Newell, Alexander Pantelyat, Manuela Pendziwiat, Annette Peters, Laura Molina‐Porcel, Alberto Rábano, Radoslav Matěj, Alex Rajput, Ali H. Rajput, Regina Reimann, William K. Scott, William W. Seeley, Sashika Selvackadunco, Tanya Simuni, Christine Stadelmann, Per Svenningsson, Alan Thomas, Claudia Trenkwalder, Claire Troakes, John Q. Trojanowski, Ryan J. Uitti, Charles L. White, Zbigniew K. Wszołek, Tao Xie, Teresa Ximelis, Justo Yebenes, Ulrich Müller, Daniela Berg, Jochen Herms, Gregor Kuhlenbäumer, Günter U. Höglinger
Publicat 2022Artigo -
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration per Julie van der Zee, Tim Van Langenhove, Gábor G. Kovács, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut, Katrien Smets, Philip Van Damme, Céline Merlin, Annelies Laureys, Marleen Van den Broeck, Maria Mattheijssens, Karin Peeters, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Isabel Hernández, Merçé Boada, Agustı́n Ruiz, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Frederico Simões do Couto, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Caroline Graff, Huei-Hsin Chiang, Håkan Thonberg, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Giovanni B. Frisoni, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Tobias B. Haack, Tim M. Strom, Holger Prokisch, Oriol Dols‐Icardo, Jordi Clarimón, Alberto Lleó, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Michael T. Heneka, Frank Jessen, Alfredo Ramı́rez, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Eva Parobková, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Thomas Ströbel, Patrick Santens, Wim Robberecht, Peter De Jonghe, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Kristel Sleegers, Christine Van Broeckhoven
Publicat 2014Artigo -
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<i>TBK1</i> Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis per Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker, Jonathan Baets, Ellen Gelpí, Ricardo Rojas-García, Jordi Clarimón, Alberto Lleó, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Robert Perneczky, Matthis Synofzik, Jennifer Just, Lüdger Schöls, Caroline Graff, Håkan Thonberg, Barbara Borroni, Alessandro Padovani, Albena Jordanova, Stayko Sarafov, Ivailo Tournev, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Frederico Simões do Couto, Alfredo Ramı́rez, Frank Jessen, Michael T. Heneka, Estrella Gómez‐Tortosa, Adrian Danek, Patrick Cras, Rik Vandenberghe, Peter De Jonghe, Peter Paul De Deyn, Kristel Sleegers, Marc Cruts, Christine Van Broeckhoven, Johan Goeman, Dirk Nuytten, Katrien Smets, Wim Robberecht, Philip Van Damme, Jan De Bleecker, Patrick Santens, Bart Dermaut, Jan Versijpt, Alex Michotte, Adrian Ivanoiu, Olivier Deryck, Bruno Bergmans, Jean Delbeck, M. Bruyland, Christiana Willems, Éric Salmon, Pau Pástor, Sara Ortega‐Cubero, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Isabel Hernández, Merçé Boada, Agustı́n Ruiz, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Raquel Sánchez‐Valle, Albert Lladó, Isabel Santana, Maria Rosário Almeida, Giovanni B. Frisoni, Walter Maetzler, Radoslav Matěj, Matthew J. Fraidakis, Gábor G. Kovács, Gian Maria Fabrizi, Silvia Testi
Publicat 2016Artigo -
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Real-world EGFR testing practices for non-small-cell lung cancer by thoracic pathology laboratories across Europe per Paul Hofman, Fiorella Calabrese, Izidor Kern, Julien Adam, Ana Alarcão, Ilaria Alborelli, N.T. Anton, Annette Arndt, A. M Avdalyan, Massimo Barberis, Hugues Bégueret, Bettina Bisig, Hélène Blons, Pontus Boström, Luka Brčić, Gordana Bubanović, A. Buisson, Anna Caliò, Maria Cannone, Lucas Resende de Carvalho, C. Caumont, Anne Cayre, L. Chalabreysse, Marie Pierre Chenard, Esther Conde, Marie‐Christine Copin, Jean‐François Côté, Nicky D’Haene, Hong Dai, Laurence de Leval, P. Delongova, Marija Denčić‐Fekete, Aurélie Fabre, F. Ferenc, Fabien Forest, Florence de Fraipont, M. Garcia-Martos, Guillaume Gauchotte, Robert Geraghty, Éric Guérin, D. Guerrero, Susana Hernández, Pavel Hurník, B. Jean-Jacques, Karl Kashofer, Daniel Kazdal, Sylvie Lantuéjoul, Camille Léonce, Antonio Lupo, Umberto Malapelle, Radoslav Matěj, Jean‐Louis Merlin, Kirsten D. Mertz, Alain Morel, Aino Mutka, Nicola Normanno, P. Ovidiu, Ángel Panizo, Mauro Papotti, Eva Parobková, Giulia Pasello, Patrick Pauwels, Giuseppe Pelosi, Frédérique Penault‐Llorca, Tiphanie Picot, Nicolas Piton, Alessandra Pittaro, G. Planchard, Nicolas Poté, Teodora Radonic, Ida Rapa, Alessandra Rappa, Cristin Roma, Mitja Rot, Jean‐Christophe Sabourin, Indra Pratama Putra Salmon, S. Savic Prince, Aldo Scarpa, Ed Schuuring, I. Serre, Vasiliki Siozopoulou, D. Sizaret, Silvana Smojver‐Ježek, Jérôme Solassol, Konrad Steinestel, Jelena Stojšić, C. Syrykh, Sergei Timofeev, Giancarlo Troncone, Arnaud Uguen, Séverine Valmary‐Degano, A. Vigier, Marco Volante, Sissel Gyrid Freim Wahl, Albrecht Stenzinger, Marius Ilié
Publicat 2023Artigo -
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A Pan‐<scp>E</scp>uropean Study of the<i>C9orf72</i>Repeat Associated with<scp>FTLD</scp>: Geographic Prevalence, Genomic Instability, and Intermediate Repeats per Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben, Veerle Bäumer, Githa Maes, Ellen Corsmit, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Sónia Pereira, José Pimentel, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Caroline Graff, Huei‐Hsin Chiang, Marie Westerlund, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Giovanni B. Frisoni, Orazio Zanetti, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Michael T. Heneka, Frank Jessen, Radoslav Matěj, Eva Parobková, Gábor G. Kovács, Thomas Ströbel, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Adrian Danek, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Patrick Santens, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Stéphanie Philtjens, Kristel Sleegers, Veerle Bäumer, Githa Maes, Ellen Corsmit, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Stéphanie Philtjens, Jessie Theuns, Kristel Sleegers, Veerle Bäumer, Githa Maes, Marc Cruts, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter P. De Deyn, Patrick Cras, Sebastiaan Engelborghs, Peter P. De Deyn, Mathieu Vandenbulcke, Mathieu Vandenbulcke, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen
Publicat 2012Revisão
Eines de cerca:
Matèries relacionades
Biology
Medicine
Pathology
Disease
Gene
Genetics
Internal medicine
Neuroscience
Dementia
Biochemistry
Cancer
Frontotemporal dementia
Immunohistochemistry
Oncology
Alpha-synuclein
Alzheimer's disease
Ataxia
Atrophy
Cancer research
Cell biology
Cerebellar ataxia
Cerebellum
Degenerative disease
Endocrinology
Frontotemporal lobar degeneration
Intensive care medicine
Molecular biology
Mutation
Olivopontocerebellar atrophy
Parkinson's disease