Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Zdenek Rohan"'
Autor:
Zuzana Stejskalova, Zdenek Rohan, Robert Rusina, Adam Tesar, Jaromir Kukal, Gabor G. Kovacs, Ales Bartos, Radoslav Matej
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background We aimed to produce a detailed neuropathological analysis of pyramidal motor system pathology and provide its clinical pathological correlation in cases with definite progressive supranuclear palsy (PSP). Methods Pyramidal motor s
Externí odkaz:
https://doaj.org/article/7f24de3257b740e4b8007af784178d02
Autor:
Adam Tesar, Zdenek Rohan, Radoslav Matej, Zuzana Stejskalova, Robert Rusina, Jaromir Kukal, Ales Bartos, Gabor G. Kovacs
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-8 (2019)
BMC Neurology
BMC Neurology
Background We aimed to produce a detailed neuropathological analysis of pyramidal motor system pathology and provide its clinical pathological correlation in cases with definite progressive supranuclear palsy (PSP). Methods Pyramidal motor system pat
Autor:
Kristel Sleegers, Nathalie Geerts, Ellen Gelpi, Lubina Dillen, Caroline Graff, Christine Van Broeckhoven, Tobi Van den Bossche, Albert Lladó, Alessandro Padovani, Sandro Sorbi, Barbara Borroni, Huei-Hsin Chiang, Benedetta Nacmias, Janine Diehl-Schmid, Jordi Clarimón, Patrick Cras, Panagiotis Alexopoulos, Håkan Thonberg, Sara Ortega-Cubero, Julie van der Zee, Radoslav Matej, Rita Cacace, Annelies Laureys, Pau Pastor, Giuliano Binetti, Maria A. Pastor, Raquel Sánchez-Valle, Maria Koutroumani, Rik Vandenberghe, Alexandre de Mendonça, Mathieu Vandenbulcke, Magda Tsolaki, Isabel Santana, Madalena Martins, Peter Paul De Deyn, Zdenek Rohan, Alberto Lleó, Roberta Ghidoni, Maria Rosário Almeida, Sebastiaan Engelborghs, Juan Fortea, Luisa Benussi
Publikováno v:
Human Mutation. 36:1226-1235
Rare variants in the phospholipase D3 gene (PLD3) were associated with increased risk for late-onset Alzheimer disease (LOAD). We identified a missense mutation in PLD3 in whole-genome sequence data of a patient with autopsy confirmed Alzheimer disea
Autor:
Juan Fortea, Marc Cruts, Tobi Van den Bossche, Jan Versijpt, Alessandro Padovani, Luisa Benussi, Roberta Ghidoni, Alexandre de Mendonça, Elena Lorenzo, Manuel Seijo-Martínez, Jaume Campdelacreu, Sandro Sorbi, Radoslav Matej, Peter Paul De Deyn, Panagiotis Alexopoulos, Olivier Deryck, Albert Lladó, Pau Pastor, Frederico Simões do Couto, Rik Vandenberghe, Estrella Gómez-Tortosa, Zdenek Rohan, Jordi Clarimón, Anne Sieben, Jordi Gascon, Isabel Santana, Maria A. Pastor, Maria Koutroumani, Madalena Martins, Sebastiaan Engelborghs, Janine Diehl-Schmid, Christine Van Broeckhoven, Benedetta Nacmias, Patrick Santens, Lubina Dillen, Ilse Gijselinck, Giuliano Binetti, Silvia Bagnoli, Bruno Bergmans, Agustín Ruiz, Raquel Sánchez-Valle, Barbara Borroni, Maria Rosário Almeida, Kristel Sleegers, Ellen Gelpi, Adrian Ivanoiu, Bavo Heeman, Cristina Razquin, Magda Tsolaki, Elena Iglesias, Caroline Graff, Johan Goeman, Alberto Lleó, Valentina Bessi, Laura Fratiglioni, Jan Verheijen, Alex Michotte, Jan De Bleecker, Rafael Blesa, Julie van der Zee, Eric Salmon, Ramón Reñé, Dirk Nuytten, Mathieu Vandenbulcke, Bart Dermaut, Håkan Thonberg, Christiana Willems
Publikováno v:
Neurobiology of Aging
Neurobiology of aging, Vol. 62, p. 245.e1-245.e7 (2018)
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging
Neurobiology of aging, Vol. 62, p. 245.e1-245.e7 (2018)
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging
TANK-binding kinase 1 (TBK1) loss-of-function (LoF) mutations are known to cause frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), often combined with memory deficits early in the disease course. We performed targeted resequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58ed5857598d419a89a3fe6fb32883e4
http://hdl.handle.net/2158/1107096
http://hdl.handle.net/2158/1107096
Autor:
Peter Paul De Deyn, Kristel Sleegers, Raquel Sánchez-Valle, Ellen Gelpi, Zdenek Rohan, Isabel Santana, Julie van der Zee, Patrick Cras, Panagiotis Alexopoulos, Madalena Martins, A. Lleo, Håkan Thonberg, Alessandro Padovani, Giuliano Binetti, Sandro Sorbi, Albert Lladó, Sebastiaan Engelborghs, Bavo Heeman, Tobi Van den Bossche, Alexandre de Mendonça, Pau Pastor, Christine Van Broeckhoven, Arne De Roeck, Maria Koutroumani, Janine Diehl-Schmid, Maria Rosário Almeida, Juan Fortea, Jasper Van Dongen, Sara Ortega-Cubero, Roberta Ghidoni, Lubina Dillen, Oriol Grau-Rivera, Estrella Gómez-Tortosa, Luisa Benussi, Maria A. Pastor, Benedetta Nacmias, Wouter De Coster, Caroline Graff, Jordi Clarimón, Magda Tsolaki, Jan Verheijen, Yalda Baradaran-Heravi, Barbara Borroni, Radoslav Matěj
Publikováno v:
Acta neuropathologica
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Acta Neuropathologica
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Acta Neuropathologica
Altres ajuts: The sponsors of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report. The research was funded in part by the European Commission Seventh Framework Programme for research, t
Autor:
Zdenek Rohan, Radoslav Matej
Publikováno v:
Archives of Pathology & Laboratory Medicine. 138:132-138
Frontotemporal lobar degenerations are clinically, genetically, and molecularly heterogeneous diseases characterized by mainly frontal and temporal atrophy and affecting behavioral, language, cognitive, and motor functions. The term frontotemporal de
Publikováno v:
Journal of neuropathology and experimental neurology. 75(12)
Pathological protein deposits in oligodendroglia are common but variable features of various neurodegenerative conditions. To evaluate oligodendrocyte response in neurodegenerative diseases (NDDs) with different extents of oligodendroglial protein de
Autor:
Jasmin Rahimi, Zdenek Rohan, Serge Weis, Gabor G. Kovacs, Nenad Mitrovic, Beata Sikorska, Istvan Kapas, Eduard Auff, Pawel P. Liberski, Radoslav Matej
Publikováno v:
Acta neuropathologica. 130(2)
Autor:
Julie van der Zee, Roberta Ghidoni, Nathalie Geerts, Huei Hsin Chiang, Giovanni B. Frisoni, Alberto Lleó, Céline Merlin, Alessandro Padovani, Maria Rosário Almeida, Christine Van Broeckhoven, Juan Fortea, Sebastiaan Engelborghs, Raquel Sánchez-Valle, Jordi Clarimón, Håkan Thonberg, Pau Pastor, Karolien Bettens, Luisa Benussi, Benedetta Nacmias, Elise Cuyvers, Giuliano Binetti, Caroline Graff, Janine Diehl-Schmid, Caroline Robberecht, Alexandre de Mendonça, Panagiotis Alexopoulos, Lubina Dillen, Sara Ortega-Cubero, Kristel Sleegers, Ellen Gelpi, Rik Vandenberghe, Sandro Sorbi, Maria A. Pastor, Barbara Borroni, Mathieu Vandenbulcke, Gian Maria Fabrizi, Peter Paul De Deyn, Zdenek Rohan, Radoslav Matěj, Isabel Santana, Madalena Martins, Agustín Ruiz, Albert Lladó
Publikováno v:
Neurobiology of Aging, Vol. 36, No 5 (2015) pp. 2005.e15-e22
Neurobiology of Aging
Neurobiology of aging
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of Aging, 36(5), 2005.e15-2005.e22. ELSEVIER SCIENCE INC
Neurobiology of Aging
Neurobiology of aging
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of Aging, 36(5), 2005.e15-2005.e22. ELSEVIER SCIENCE INC
Meta-analysis of existing genome-wide association studies on Alzheimer's disease (AD) showed subgenome-wide association of an intronic variant in the sequestosome 1 (SQSTM1) gene with AD. We performed targeted resequencing of SQSTM1 in Flanders-Belgi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f26161a4583716c3b1b6e1f51bd850c
https://archive-ouverte.unige.ch/unige:75880
https://archive-ouverte.unige.ch/unige:75880
Publikováno v:
The Journal of pathology. 236(1)