Zobrazeno 1 - 10
of 280
pro vyhledávání: '"Leonel T"'
Autor:
Imogen J. Swift, Rosa Rademakers, NiCole Finch, Matt Baker, Roberta Ghidoni, Luisa Benussi, Giuliano Binetti, Giacomina Rossi, Matthis Synofzik, Carlo Wilke, David Mengel, Caroline Graff, Leonel T. Takada, Raquel Sánchez-Valle, Anna Antonell, Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Marina Arcaro, Stefanie Schreiber, Stefan Vielhaber, Philipp Arndt, Isabel Santana, Maria Rosario Almeida, Fermín Moreno, Myriam Barandiaran, Alazne Gabilondo, Johannes Stubert, Estrella Gómez-Tortosa, Pablo Agüero, M. José Sainz, Tomohito Gohda, Maki Murakoshi, Nozomu Kamei, Sarah Kittel-Schneider, Andreas Reif, Johannes Weigl, Jinlong Jian, Chuanju Liu, Ginette Serrero, Thomas Greither, Gerit Theil, Ebba Lohmann, Stefano Gazzina, Silvia Bagnoli, Giovanni Coppola, Amalia Bruni, Mirja Quante, Wieland Kiess, Andreas Hiemisch, Anne Jurkutat, Matthew S. Block, Aaron M. Carlson, Geir Bråthen, Sigrid Botne Sando, Gøril Rolfseng Grøntvedt, Camilla Lauridsen, Amanda Heslegrave, Carolin Heller, Emily Abel, Alba Gómez-Núñez, Roger Puey, Andrea Arighi, Enmanuela Rotondo, Lize C. Jiskoot, Lieke H. H. Meeter, João Durães, Marisa Lima, Miguel Tábuas-Pereira, João Lemos, Bradley Boeve, Ronald C. Petersen, Dennis W. Dickson, Neill R. Graff-Radford, Isabelle LeBer, Leila Sellami, Foudil Lamari, Fabienne Clot, Barbara Borroni, Valentina Cantoni, Jasmine Rivolta, Alberto Lleó, Juan Fortea, Daniel Alcolea, Ignacio Illán-Gala, Lucie Andres-Cerezo, Philip Van Damme, Jordi Clarimon, Petra Steinacker, Emily Feneberg, Markus Otto, Emma L. van der Ende, John C. van Swieten, Harro Seelaar, Henrik Zetterberg, Aitana Sogorb-Esteve, Jonathan D. Rohrer
Publikováno v:
Alzheimer’s Research & Therapy, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Background Pathogenic heterozygous mutations in the progranulin gene (GRN) are a key cause of frontotemporal dementia (FTD), leading to significantly reduced biofluid concentrations of the progranulin protein (PGRN). This has led to a number
Externí odkaz:
https://doaj.org/article/1d7c751ac55c494a90e49ef788756561
Autor:
Carla Abdelnour, Federica Agosta, Marco Bozzali, Bertrand Fougère, Atsushi Iwata, Ramin Nilforooshan, Leonel T. Takada, Félix Viñuela, Martin Traber
Publikováno v:
Alzheimer’s Research & Therapy, Vol 14, Iss 1, Pp 1-12 (2022)
Abstract Background Patient stratification is the division of a patient population into distinct subgroups based on the presence or absence of particular disease characteristics. As patient stratification can be used to account for the underlying pat
Externí odkaz:
https://doaj.org/article/0963a2d230184043a8bac0dc179f9674
Autor:
Marcelo Adrián Maito, Hernando Santamaría-García, Sebastián Moguilner, Katherine L. Possin, María E. Godoy, José Alberto Avila-Funes, María I. Behrens, Ignacio L. Brusco, Martín A. Bruno, Juan F. Cardona, Nilton Custodio, Adolfo M. García, Shireen Javandel, Francisco Lopera, Diana L. Matallana, Bruce Miller, Maira Okada de Oliveira, Stefanie D. Pina-Escudero, Andrea Slachevsky, Ana L. Sosa Ortiz, Leonel T. Takada, Enzo Tagliazuchi, Victor Valcour, Jennifer S. Yokoyama, Agustín Ibañez
Publikováno v:
The Lancet Regional Health. Americas, Vol 17, Iss , Pp 100387- (2023)
Summary: Background: Global brain health initiatives call for improving methods for the diagnosis of Alzheimer's disease (AD) and frontotemporal dementia (FTD) in underrepresented populations. However, diagnostic procedures in upper-middle-income cou
Externí odkaz:
https://doaj.org/article/4ec51759945747fbaaabc9db03fca988
Autor:
Claudia Duran-Aniotz, Paulina Orellana, Tomas Leon Rodriguez, Fernando Henriquez, Victoria Cabello, María F. Aguirre-Pinto, Tamara Escobedo, Leonel T. Takada, Stefanie D. Pina-Escudero, Oscar Lopez, Jennifer S. Yokoyama, Agustin Ibanez, Mario A. Parra, Andrea Slachevsky
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Frontotemporal dementia (FTD) includes a group of clinically, genetically, and pathologically heterogeneous neurodegenerative disorders, affecting the fronto-insular-temporal regions of the brain. Clinically, FTD is characterized by progressive defic
Externí odkaz:
https://doaj.org/article/8eff1edc95a64035ba74af1ffa80104b
Autor:
Agustin Ibanez, Jennifer S. Yokoyama, Katherine L. Possin, Diana Matallana, Francisco Lopera, Ricardo Nitrini, Leonel T. Takada, Nilton Custodio, Ana Luisa Sosa Ortiz, José Alberto Avila-Funes, Maria Isabel Behrens, Andrea Slachevsky, Richard M. Myers, J. Nicholas Cochran, Luis Ignacio Brusco, Martin A. Bruno, Sonia M. D. Brucki, Stefanie Danielle Pina-Escudero, Maira Okada de Oliveira, Patricio Donnelly Kehoe, Adolfo M. Garcia, Juan Felipe Cardona, Hernando Santamaria-Garcia, Sebastian Moguilner, Claudia Duran-Aniotz, Enzo Tagliazucchi, Marcelo Maito, Erika Mariana Longoria Ibarrola, Maritza Pintado-Caipa, Maria Eugenia Godoy, Vera Bakman, Shireen Javandel, Kenneth S. Kosik, Victor Valcour, Bruce L. Miller
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Dementia is becoming increasingly prevalent in Latin America, contrasting with stable or declining rates in North America and Europe. This scenario places unprecedented clinical, social, and economic burden upon patients, families, and health systems
Externí odkaz:
https://doaj.org/article/a2e4fdf9c3cc48448e116e091fd05800
Autor:
Jennifer S Yokoyama, Allen K L Lee, Leonel T Takada, Edgar Busovaca, Luke W Bonham, Steven Z Chao, Marian Tse, Jing He, Christopher G Schwarz, Owen T Carmichael, Brandy R Matthews, Anna Karydas, Michael W Weiner, Giovanni Coppola, Charles S DeCarli, Bruce L Miller, Howard J Rosen
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0118338 (2015)
Studying ethnically diverse groups is important for furthering our understanding of biological mechanisms of disease that may vary across human populations. The ε4 allele of apolipoprotein E (APOE ε4) is a well-established risk factor for Alzheimer
Externí odkaz:
https://doaj.org/article/7bea0dcb2ab04fc9befe88c99671dc1b
Akademický článek
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Akademický článek
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Autor:
Mirna Lie Hosogi Senaha, Paulo Caramelli, Sonia M.D. Brucki, Jerusa Smid, Leonel T. Takada, Claudia S. Porto, Karolina G. César, Maria Niures P. Matioli, Roger T. Soares, Letícia L. Mansur, Ricardo Nitrini
Publikováno v:
Dementia & Neuropsychologia, Vol 7, Iss 1, Pp 110-121
ABSTRACT Primary progressive aphasia (PPA) is a neurodegenerative clinical syndrome characterized primarily by progressive language impairment. Recently, consensus diagnostic criteria were published for the diagnosis and classification of variants of
Externí odkaz:
https://doaj.org/article/1b43b5af59ac467ea7559e428423360a