Works matching AU Iruzubieta, Pablo


Results: 21
    1
    2

    Additional Cover.

    Published in:
    Aging Cell, 2025, v. 24, n. 1, p. 1, doi. 10.1111/acel.14480
    By:
    • Launay, Nathalie;
    • Espinosa‐Alcantud, Maria;
    • Verdura, Edgard;
    • Fernández‐Eulate, Gorka;
    • Ondaro, Jon;
    • Iruzubieta, Pablo;
    • Marsal, Maria;
    • Schlüter, Agatha;
    • Ruiz, Montserrat;
    • Fourcade, Stephane;
    • Rodríguez‐Palmero, Agustí;
    • Zulaica, Miren;
    • Sistiaga, Andone;
    • Labayru, Garazi;
    • Loza‐Alvarez, Pablo;
    • Vaquero, Alejandro;
    • Lopez de Munain, Adolfo;
    • Pujol, Aurora
    Publication type:
    Article
    3

    Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia.

    Published in:
    Aging Cell, 2025, v. 24, n. 1, p. 1, doi. 10.1111/acel.14355
    By:
    • Launay, Nathalie;
    • Espinosa‐Alcantud, Maria;
    • Verdura, Edgard;
    • Fernández‐Eulate, Gorka;
    • Ondaro, Jon;
    • Iruzubieta, Pablo;
    • Marsal, Maria;
    • Schlüter, Agatha;
    • Ruiz, Montserrat;
    • Fourcade, Stephane;
    • Rodríguez‐Palmero, Agustí;
    • Zulaica, Miren;
    • Sistiaga, Andone;
    • Labayru, Garazi;
    • Loza‐Alvarez, Pablo;
    • Vaquero, Alejandro;
    • Lopez de Munain, Adolfo;
    • Pujol, Aurora
    Publication type:
    Article
    4
    5
    6
    7

    Impact on functional outcome of an adaptive Stroke Unit based system of care for patients undergoing endovascular treatment during pandemic times.

    Published in:
    European Stroke Journal, 2022, v. 7, n. 3, p. 248, doi. 10.1177/23969873221098269
    By:
    • Equiza, Jon;
    • de la Riva, Patricia;
    • Angel Larrea, José;
    • Marta-Enguita, Juan;
    • Albájar, Inés;
    • Lüttich, Alex;
    • Garmendia, Eñaut;
    • Alonso, Maitane;
    • de Arce, Ana;
    • Díez, Noemí;
    • Gonzalez, Félix;
    • Iruzubieta, Pablo;
    • Sulibarria, Naroa;
    • Puig, Josep;
    • Martínez-Zabaleta, Maite
    Publication type:
    Article
    8
    9

    Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-36654-8
    By:
    • Bonnet, Céline;
    • Pellerin, David;
    • Roth, Virginie;
    • Clément, Guillemette;
    • Wandzel, Marion;
    • Lambert, Laëtitia;
    • Frismand, Solène;
    • Douarinou, Marian;
    • Grosset, Anais;
    • Bekkour, Ines;
    • Weber, Frédéric;
    • Girardier, Florent;
    • Robin, Clément;
    • Cacciatore, Stéphanie;
    • Bronner, Myriam;
    • Pourié, Carine;
    • Dreumont, Natacha;
    • Puisieux, Salomé;
    • Iruzubieta, Pablo;
    • Dicaire, Marie-Josée
    Publication type:
    Article
    10

    The FGF14GAA repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the SCA27B phenotype across populations.

    Published in:
    Clinical Genetics, 2024, v. 105, n. 4, p. 446, doi. 10.1111/cge.14482
    By:
    • Kartanou, Chrisoula;
    • Mitrousias, Alexandros;
    • Pellerin, David;
    • Kontogeorgiou, Zoi;
    • Iruzubieta, Pablo;
    • Dicaire, Marie‐Josée;
    • Danzi, Matt C.;
    • Koniari, Chrysoula;
    • Athanassopoulos, Konstantinos;
    • Panas, Marios;
    • Stefanis, Leonidas;
    • Zuchner, Stephan;
    • Brais, Bernard;
    • Houlden, Henry;
    • Karadima, Georgia;
    • Koutsis, Georgios
    Publication type:
    Article
    11

    Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like features.

    Published in:
    Brain: A Journal of Neurology, 2024, v. 147, n. 8, p. 2867, doi. 10.1093/brain/awae046
    By:
    • Iruzubieta, Pablo;
    • Damborenea, Alberto;
    • Ioghen, Mihaela;
    • Bajew, Simon;
    • Fernandez-Torrón, Roberto;
    • Töpf, Ana;
    • Herrero-Reiriz, Álvaro;
    • Epure, Diana;
    • Vill, Katharina;
    • Hernández-Laín, Aurelio;
    • Manterola, María;
    • Azkargorta, Mikel;
    • Pikatza-Menoio, Oihane;
    • Pérez-Fernandez, Laura;
    • García-Puga, Mikel;
    • Gaina, Gisela;
    • Bastian, Alexandra;
    • Streata, Ioana;
    • Walter, Maggie C;
    • Müller-Felber, Wolfgang
    Publication type:
    Article
    12

    A founder variant in the RYR1 gene is associated with hyperCKemia, myalgia and muscle cramps.

    Published in:
    European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16471
    By:
    • Segarra‐Casas, Alba;
    • Iruzubieta, Pablo;
    • Kapetanovic, Solange;
    • Hernández‐Laín, Aurelio;
    • Jericó, Ivonne;
    • Fernández‐Torrón, Roberto;
    • Maneiro, Miren;
    • Marco‐Moreno, Pablo;
    • Zelaya‐Huerta, M. Victoria;
    • Rodríguez‐Santiago, Benjamín;
    • Calafell, Francesc;
    • Töpf, Ana;
    • Straub, Volker;
    • Vallejo‐Illarramendi, Ainara;
    • López de Munain, Adolfo;
    • Gallano, Pia;
    • Gonzalez‐Quereda, Lidia
    Publication type:
    Article
    13

    Frequency and phenotypic spectrum of spinocerebellar ataxia 27B and other genetic ataxias in a Spanish cohort of late‐onset cerebellar ataxia.

    Published in:
    European Journal of Neurology, 2023, v. 30, n. 12, p. 3828, doi. 10.1111/ene.16039
    By:
    • Iruzubieta, Pablo;
    • Pellerin, David;
    • Bergareche, Alberto;
    • Albajar, Inés;
    • Mondragón, Elisabet;
    • Vinagre, Ana;
    • Fernández‐Torrón, Roberto;
    • Moreno, Fermín;
    • Equiza, Jon;
    • Campo‐Caballero, David;
    • Poza, Juan José;
    • Ruibal, Marta;
    • Formica, Alessandro;
    • Dicaire, Marie‐Josée;
    • Danzi, Matt C.;
    • Zuchner, Stephan;
    • Croitoru, Ioana;
    • Ruiz, Montserrat;
    • Schlüter, Agatha;
    • Casasnovas, Carlos
    Publication type:
    Article
    14
    15

    Serum Neurofilament Light Chain in Replication Factor Complex Subunit 1 CANVAS and Disease Spectrum.

    Published in:
    Movement Disorders, 2024, v. 39, n. 1, p. 209, doi. 10.1002/mds.29680
    By:
    • Quartesan, Ilaria;
    • Vegezzi, Elisa;
    • Currò, Riccardo;
    • Heslegrave, Amanda;
    • Pisciotta, Chiara;
    • Iruzubieta, Pablo;
    • Salvalaggio, Alessandro;
    • Fernández‐Eulate, Gorka;
    • Dominik, Natalia;
    • Rugginini, Bianca;
    • Manini, Arianna;
    • Abati, Elena;
    • Facchini, Stefano;
    • Manso, Katarina;
    • Albajar, Ines;
    • Laban, Rhiannon;
    • Rossor, Alexander M.;
    • Pichiecchio, Anna;
    • Cosentino, Giuseppe;
    • Saveri, Paola
    Publication type:
    Article
    16

    Non‐GAA Repeat Expansions in FGF14 Are Likely Not Pathogenic—Reply to: "Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean Family".

    Published in:
    Movement Disorders, 2023, v. 38, n. 8, p. 1575, doi. 10.1002/mds.29552
    By:
    • Pellerin, David;
    • Iruzubieta, Pablo;
    • Tekgül, Şeyma;
    • Danzi, Matt C.;
    • Ashton, Catherine;
    • Dicaire, Marie‐Josée;
    • Wandzel, Marion;
    • Roth, Virginie;
    • Lamont, Phillipa J.;
    • Bonnet, Céline;
    • Renaud, Mathilde;
    • Synofzik, Matthis;
    • Zuchner, Stephan;
    • Brais, Bernard;
    • Başak, Nazlı A.;
    • Houlden, Henry
    Publication type:
    Article
    17

    The Role of Integrin β1D Mislocalization in the Pathophysiology of Calpain 3-Related Limb–Girdle Muscular Dystrophy.

    Published in:
    Cells (2073-4409), 2025, v. 14, n. 6, p. 446, doi. 10.3390/cells14060446
    By:
    • Valls, Andrea;
    • Ruiz-Roldán, Cristina;
    • Immanuel, Jenita;
    • Alonso-Martín, Sonia;
    • Gallardo, Eduard;
    • Fernández-Torrón, Roberto;
    • Bonilla, Mario;
    • Lersundi, Ana;
    • Hernández-Laín, Aurelio;
    • Domínguez-González, Cristina;
    • Vílchez, Juan Jesús;
    • Iruzubieta, Pablo;
    • López de Munain, Adolfo;
    • Sáenz, Amets
    Publication type:
    Article
    18
    19

    Clinical and imaging spectrum of non-congenital dominant ACTN2 myopathy.

    Published in:
    Journal of Neurology, 2025, v. 272, n. 2, p. 1, doi. 10.1007/s00415-025-12893-9
    By:
    • Iruzubieta, Pablo;
    • Verdú-Díaz, José;
    • Töpf, Ana;
    • Luce, Leonela;
    • Claeys, Kristl G.;
    • De Ridder, Willem;
    • González-Quereda, Lidia;
    • de Fuenmayor-Fernández de la Hoz, Carlos Pablo;
    • Poza, Juan José;
    • Zulaica, Miren;
    • de Jonghe, Peter;
    • Duff, Jennifer;
    • Mroczek, Magdalena;
    • Martín-Jiménez, Paloma;
    • Hernández-Laín, Aurelio;
    • Domínguez-González, Cristina;
    • Baets, Jonathan;
    • Gallano, Pia;
    • Díaz-Manera, Jordi;
    • Straub, Volker
    Publication type:
    Article
    20

    Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis.

    Published in:
    Acta Neuropathologica, 2024, v. 148, n. 1, p. 1, doi. 10.1007/s00401-024-02794-y
    By:
    • Zufiría, Mónica;
    • Pikatza-Menoio, Oihane;
    • Garciandia-Arcelus, Maddi;
    • Bengoetxea, Xabier;
    • Jiménez, Andrés;
    • Elicegui, Amaia;
    • Levchuk, María;
    • Arnold-García, Olatz;
    • Ondaro, Jon;
    • Iruzubieta, Pablo;
    • Rodríguez-Gómez, Laura;
    • Fernández-Pelayo, Uxoa;
    • Muñoz-Oreja, Mikel;
    • Aiastui, Ana;
    • García-Verdugo, José Manuel;
    • Herranz-Pérez, Vicente;
    • Zulaica, Miren;
    • Poza, Juan José;
    • Ruiz-Onandi, Rebeca;
    • Fernández-Torrón, Roberto
    Publication type:
    Article
    21