Zobrazeno 1 - 10
of 182
pro vyhledávání: '"A. PELAYO-NEGRO"'
Autor:
Armirola-Ricaurte, Camila, Zonnekein, Noortje, Koutsis, Georgios, Amor-Barris, Silvia, Pelayo-Negro, Ana Lara, Atkinson, Derek, Efthymiou, Stephanie, Turchetti, Valentina, Dinopoulos, Argyris, Garcia, Antonio, Karakaya, Mert, Moris, German, Polat, Ayşe Ipek, Yiş, Uluç, Espinos, Carmen, Van de Vondel, Liedewei, De Vriendt, Els, Karadima, Georgia, Wirth, Brunhilde, Hanna, Michael, Houlden, Henry, Berciano, Jose, Jordanova, Albena
Publikováno v:
In Genetics in Medicine June 2024 26(6)
Autor:
Aldecoa, Iban, Barcelo, Maria Ines, Canneti, Beatrice, Cedres, Susana, Chavarria, Alba, Fabregat-Franco, Carles, Ferrer-Civeira, Maria, Frutos-Alegria, Maria Teresa, Guasp, Mar, Landete, Lamberto, Llufriu, Sara, Marti, Maria Teresa, Martinez-Rodriguez, Jose Enrique, Matas-Garcia, Ana, Moreno-Pulido, Silvia, Pelayo-Negro, Ana Lara, Reig, Maria, Riancho, Javier, Sánchez-Vizcaíno, Cristina, Sanduzzi-Zamparelli, Marco, Sepulveda, Maria, Silvarrey-Rodriguez, Saul, Tagliani, Paula, Fonseca, Elianet *, Cabrera-Maqueda, Jose M *, Ruiz-García, Raquel, Naranjo, Laura, Diaz-Pedroche, Carmen, Velasco, Roser, Macias-Gómez, Adrià, Milisenda, Jose C, Muñoz-Farjas, Elena, Pascual-Goñi, Elba, Gállego Perez-Larraya, Jaime, Saiz, Albert, Dalmau, Josep, Blanco, Yolanda, Graus, Francesc, Martinez-Hernandez, Eugenia *
Publikováno v:
In The Lancet Neurology December 2023 22(12):1150-1159
Autor:
Prieto-Peña, Diana, Ocejo-Vinyals, Javier G., Mazariegos-Cano, Joel, Pelayo-Negro, Ana L., Remuzgo-Martínez, Sara, Genre, Fernanda, García-Dorta, Alicia, Renuncio-García, Mónica, Martínez-Taboada, Víctor M., García-Ibarbia, Carmen, Sánchez-Martín, Julio, López-Hoyos, Marcos, Blanco, Ricardo, González-Gay, Miguel A., Hernández, José L.
Publikováno v:
In European Journal of Internal Medicine July 2022 101:86-92
Autor:
Elena Cortés‐Vicente, Rodrigo Álvarez‐Velasco, Francesc Pla‐Junca, Ricard Rojas‐Garcia, Carmen Paradas, Teresa Sevilla, Carlos Casasnovas, María Teresa Gómez‐Caravaca, Julio Pardo, Alba Ramos‐Fransi, Ana Lara Pelayo‐Negro, Gerardo Gutiérrez‐Gutiérrez, Janina Turon‐Sans, Adolfo López de Munain, Antonio Guerrero‐Sola, Ivonne Jericó, María Asunción Martín, María Dolores Mendoza, Germán Morís, Beatriz Vélez‐Gómez, Tania Garcia‐Sobrino, Elba Pascual‐Goñi, David Reyes‐Leiva, Isabel Illa, Eduard Gallardo
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 2, Pp 122-131 (2022)
Abstract Objective To describe the clinical characteristics and outcomes in patients with refractory myasthenia gravis (MG) and to determine the effectiveness and side effects of the drugs used for their treatment. Methods This observational retrospe
Externí odkaz:
https://doaj.org/article/2b39a018049e4bdbb38862338fe7dbf0
Akademický článek
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Autor:
Berciano, José, Orizaola, Pedro, Gallardo, Elena, Pelayo-Negro, Ana L., Sánchez-Juan, Pascual, Infante, Jon, Sedano, María J.
Publikováno v:
In Clinical Neurophysiology Practice 2020 5:1-9
Autor:
José Berciano, Pedro Orizaola, Elena Gallardo, Ana L. Pelayo-Negro, Pascual Sánchez-Juan, Jon Infante, María J. Sedano
Publikováno v:
Clinical Neurophysiology Practice, Vol 5, Iss , Pp 1-9 (2020)
Objectives: Using recent optimized electrodiagnostic criteria sets, we primarily aimed at verifying the accuracy of the initial electrophysiological test in very early Guillain-Barré syndrome (VEGBS), ≤4 days of onset, compared with the results of
Externí odkaz:
https://doaj.org/article/38b120c5a66f4199882261b4fc8e5269
Autor:
E. Servián-Morilla, M. Cabrera-Serrano, E. Rivas-Infante, A. Carvajal, P. J. Lamont, A. L. Pelayo-Negro, G. Ravenscroft, R. Junckerstorff, J. M. Dyke, S. Fletcher, A. M. Adams, F. Mavillard, M. A. Fernández-García, J. L. Nieto-González, N. G. Laing, C. Paradas
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-16 (2019)
Abstract TRIM32 is a E3 ubiquitin -ligase containing RING, B-box, coiled-coil and six C-terminal NHL domains. Mutations involving NHL and coiled-coil domains result in a pure myopathy (LGMD2H/STM) while the only described mutation in the B-box domain
Externí odkaz:
https://doaj.org/article/347882b61d064fd4ae84598c7da1fafa
Autor:
Santana, Magda M., Gaspar, Laetitia S., Pinto, Maria M., Silva, Patrick, Adão, Diana, Pereira, Dina, Ribeiro, Joana Afonso, Cunha, Inês, Huebener-Schmid, Jeannette, Raposo, Mafalda, Ferreira, Ana F., Faber, Jennifer, Kuhs, Sandra, Garcia-Moreno, Hector, Reetz, Kathrin, Thieme, Andreas, Infante, Jon, Warrenburg, Bart P. C. van de, Giunti, Paola, Riess, Olaf, Schöls, Ludger, Lima, Manuela, Klockgether, Thomas, Januário, Cristina, Almeida, Luís Pereira de, Krahe, Janna, Gaalen, Judith van, Gonzalez-Robles, Cristina, Fleszar, Zofia, Pelayo-Negro, Ana Lara, Manrique, Leire, Timmann-Braun, Dagmar, Steiner, Katharina M., Melo, Ana Rosa Vieira, van de Warrenburg, Bart P. C., de Almeida, Luís Pereira, van Gaalen, Judith
Publikováno v:
Neuropathology & applied neurobiology 49(2), e12892 (2023). doi:10.1111/nan.12892
Neuropathology and Applied Neurobiology, 49
Neuropathology and Applied Neurobiology, 49, 2
Neuropathology and Applied Neurobiology, 49
Neuropathology and Applied Neurobiology, 49, 2
Contains fulltext : 292317.pdf (Publisher’s version ) (Open Access) The European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative (ESMI) is a consortium established with the ambition to set up the largest European longitudinal trial-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61e4f6f4d14ead1199ce864237a3af1e
https://pub.dzne.de/record/257792
https://pub.dzne.de/record/257792
Autor:
Rafael Sivera, Marina Frasquet, Vincenzo Lupo, Tania García-Sobrino, Patricia Blanco-Arias, Julio Pardo, Roberto Fernández-Torrón, Adolfo López de Munain, Celedonio Márquez-Infante, Liliana Villarreal, Pilar Carbonell, Ricard Rojas-García, Sonia Segovia, Isabel Illa, Anna Lia Frongia, Andrés Nascimento, Carlos Ortez, María del Mar García-Romero, Samuel Ignacio Pascual, Ana Lara Pelayo-Negro, José Berciano, Antonio Guerrero, Carlos Casasnovas, Ana Camacho, Jesús Esteban, María José Chumillas, Marisa Barreiro, Carmen Díaz, Francesc Palau, Juan Jesús Vílchez, Carmen Espinós, Teresa Sevilla
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Mutations in the GDAP1 gene can cause Charcot-Marie-Tooth disease. These mutations are quite rare in most Western countries but not so in certain regions of Spain or other Mediterranean countries. This cross-sectional retrospective multicent
Externí odkaz:
https://doaj.org/article/0faa7f5c1e624b5b885d1c7b72e34039