Works matching AU Rivas, Eloy

Results: 38
    1

    Sex Hormone Receptor Expression in Craniopharyngiomas and Association with Tumor Aggressiveness Characteristics.

    Published in:
    Journal of Clinical Medicine, 2022, v. 11, n. 1, p. 281, doi. 10.3390/jcm11010281
    By:
    • Martínez-Ortega, Antonio;
    • Flores-Martinez, Álvaro;
    • Venegas-Moreno, Eva;
    • Dios, Elena;
    • Del Can, Diego;
    • Rivas, Eloy;
    • Kaen, Ariel;
    • Cárdenas Ruiz-Valdepeñas, Eugenio;
    • Fajardo, Elena;
    • Roldán, Florinda;
    • González-Rivera, Natividad;
    • Oliva, Rosario;
    • Fernández-Peña, José Ignacio;
    • Soto-Moreno, Alfonso;
    • Cano, David A.
    Publication type:
    Article
    2
    3
    4
    5

    Bone marrow cellular cannibalism by medulloblastoma.

    Published in:
    American Journal of Hematology, 2015, v. 90, n. 5, p. 466, doi. 10.1002/ajh.23892
    By:
    • Escamilla, Virginia;
    • Franco-Macías, Emilio;
    • Calderón-Cabrera, Cristina;
    • Rivas, Eloy;
    • Morales-Camacho, Rosario M.;
    • Vargas, Maria Teresa;
    • Bernal, Ricardo;
    • Pérez-Simón, José A.
    Publication type:
    Article
    6
    7
    8

    Congenital hypomyelinating neuropathy due to a novel MPZ mutation.

    Published in:
    Journal of the Peripheral Nervous System, 2011, v. 16, n. 4, p. 347, doi. 10.1111/j.1529-8027.2011.00369.x
    By:
    • Sevilla, Teresa;
    • Lupo, Vincenzo;
    • Sivera, Rafael;
    • Marco-Marín, Clara;
    • Martínez-Rubio, Dolores;
    • Rivas, Eloy;
    • Hernández, Arturo;
    • Palau, Francesc;
    • Espinós, Carmen
    Publication type:
    Article
    9
    10
    11

    Lessons learned from a sporadic FUSopathy in a young man: a case report.

    Published in:
    BMC Neurology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12883-023-03082-0
    By:
    • García-Roldán, Ernesto;
    • Rivas-Infante, Eloy;
    • Medina-Rodríguez, Manuel;
    • Arriola-Infante, José Enrique;
    • Rodrigo-Herrero, Silvia;
    • Paradas, Carmen;
    • Rábano-Gutiérrez, Alberto;
    • Franco-Macías, Emilio
    Publication type:
    Article
    12

    Hemimegalencephaly: Prenatal Diagnosis and Outcome.

    Published in:
    Fetal Diagnosis & Therapy, 2011, v. 30, n. 3, p. 234, doi. 10.1159/000329937
    By:
    • Alvarez, Rosa María;
    • García-Díaz, Lutgardo;
    • Márquez, Javier;
    • Fajardo, Manuel;
    • Rivas, Eloy;
    • García-Lozano, Juan Carlos;
    • Antiñolo, Guillermo
    Publication type:
    Article
    13

    Screening of effective pharmacological treatments for MELAS syndrome using yeasts, fibroblasts and cybrid models of the disease.

    Published in:
    British Journal of Pharmacology, 2012, v. 167, n. 6, p. 1311, doi. 10.1111/j.1476-5381.2012.02086.x
    By:
    • Garrido-Maraver, Juan;
    • Cordero, Mario D;
    • Moñino, Irene Domínguez;
    • Pereira-Arenas, Sheila;
    • Lechuga-Vieco, Ana V;
    • Cotán, David;
    • De la Mata, Mario;
    • Oropesa-Ávila, Manuel;
    • De Miguel, Manuel;
    • Bautista Lorite, Juan;
    • Rivas Infante, Eloy;
    • Álvarez-Dolado, Manuel;
    • Navas, Plácido;
    • Jackson, Sandra;
    • Francisci, Silvia;
    • Sánchez-Alcázar, José A
    Publication type:
    Article
    14
    15

    Inflammatory bowel disease induces pathological α‐synuclein aggregation in the human gut and brain.

    Published in:
    Neuropathology & Applied Neurobiology, 2024, v. 50, n. 1, p. 1, doi. 10.1111/nan.12962
    By:
    • Espinosa‐Oliva, Ana M.;
    • Ruiz, Rocío;
    • Soto, Manuel Sarmiento;
    • Boza‐Serrano, Antonio;
    • Rodriguez‐Perez, Ana I.;
    • Roca‐Ceballos, María A.;
    • García‐Revilla, Juan;
    • Santiago, Marti;
    • Serres, Sébastien;
    • Economopoulus, Vasiliki;
    • Carvajal, Ana E.;
    • Vázquez‐Carretero, María D.;
    • García‐Miranda, Pablo;
    • Klementieva, Oxana;
    • Oliva‐Martín, María J.;
    • Deierborg, Tomas;
    • Rivas, Eloy;
    • Sibson, Nicola R.;
    • Labandeira‐García, José L.;
    • Machado, Alberto
    Publication type:
    Article
    16
    17

    A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss.

    Published in:
    EMBO Molecular Medicine, 2016, v. 8, n. 11, p. 1289, doi. 10.15252/emmm.201505815
    By:
    • Servián‐Morilla, Emilia;
    • Takeuchi, Hideyuki;
    • Lee, Tom V;
    • Clarimon, Jordi;
    • Mavillard, Fabiola;
    • Area‐Gómez, Estela;
    • Rivas, Eloy;
    • Nieto‐González, Jose L;
    • Rivero, Maria C;
    • Cabrera‐Serrano, Macarena;
    • Gómez‐Sánchez, Leonardo;
    • Martínez‐López, Jose A;
    • Estrada, Beatriz;
    • Márquez, Celedonio;
    • Morgado, Yolanda;
    • Suárez‐Calvet, Xavier;
    • Pita, Guillermo;
    • Bigot, Anne;
    • Gallardo, Eduard;
    • Fernández‐Chacón, Rafael
    Publication type:
    Article
    18

    Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy.

    Published in:
    2012
    By:
    • Juan-Mateu, Jonàs;
    • Rodríguez, Maria José;
    • Nascimento, Andrés;
    • Jiménez-Mallebrera, Cecilia;
    • González-Quereda, Lidia;
    • Rivas, Eloy;
    • Paradas, Carmen;
    • Madruga, Marcos;
    • Sánchez-Ayaso, Pedro;
    • Jou, Cristina;
    • González-Mera, Laura;
    • Munell, Francina;
    • Roig-Quilis, Manuel;
    • Rabasa, Maria;
    • Hernández-Lain, Aurelio;
    • Díaz-Manera, Jorge;
    • Gallardo, Eduard;
    • Pascual, Jordi;
    • Verdura, Edgard;
    • Colomer, Jaume
    Publication type:
    journal article
    19

    Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy.

    Published in:
    Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 82, doi. 10.1186/1750-1172-7-82
    By:
    • Juan-Mateu, Jonàs;
    • Rodríguez, Maria José;
    • Nascimento, Andrés;
    • Jiménez-Mallebrera, Celilia;
    • González-Quereda, Lidia;
    • Rivas, Eloy;
    • Paradas, Carmen;
    • Madruga, Marcos;
    • Sánchez-Ayaso, Pedro;
    • Jou, Cristina;
    • González-Mera, Jorge;
    • Munell, Francina;
    • Roig-Quilis, Manuel;
    • Rabasa, Maria;
    • Hernández-Lain, Aurelio;
    • Díaz-Manera, Jorge;
    • Gallardo, Eduard;
    • Pascual, Jordi;
    • Verdura, Edgard;
    • Colomer, Jaume
    Publication type:
    Article
    20
    21
    22

    HMGCS1 variants cause rigid spine syndrome amenable to mevalonic acid treatment in an animal model.

    Published in:
    Brain: A Journal of Neurology, 2025, v. 148, n. 5, p. 1707, doi. 10.1093/brain/awae371
    By:
    • Dofash, Lein N H;
    • Miles, Lee B;
    • Saito, Yoshihiko;
    • Rivas, Eloy;
    • Calcinotto, Vanessa;
    • Oveissi, Sara;
    • Serrano, Rita J;
    • Templin, Rachel;
    • Ramm, Georg;
    • Rodger, Alison;
    • Haywood, Joel;
    • Ingley, Evan;
    • Clayton, Joshua S;
    • Taylor, Rhonda L;
    • Folland, Chiara L;
    • Groth, David;
    • Hock, Daniella H;
    • Stroud, David A;
    • Gorokhova, Svetlana;
    • Donkervoort, Sandra
    Publication type:
    Article
    23

    Decoding the muscle transcriptome of patients with late-onset Pompe disease reveals markers of disease progression.

    Published in:
    Brain: A Journal of Neurology, 2024, v. 147, n. 12, p. 4213, doi. 10.1093/brain/awae249
    By:
    • Monceau, Alexandra;
    • Nath, Rasya Gokul;
    • Suárez-Calvet, Xavier;
    • Musumeci, Olimpia;
    • Toscano, Antonio;
    • Kierdaszuk, Biruta;
    • Kostera-Pruszczyk, Anna;
    • Domínguez-González, Cristina;
    • Hernández-Lain, Aurelio;
    • Paradas, Carmen;
    • Rivas, Eloy;
    • Papadimas, George;
    • Papadopoulos, Constantinos;
    • Chrysanthou-Piterou, Margarita;
    • Gallardo, Eduard;
    • Olivé, Montse;
    • Lilleker, James;
    • Roberts, Mark E;
    • Marchese, Domenica;
    • Lunazzi, Giulia
    Publication type:
    Article
    24

    Ablation of the carboxy-terminal end of MAMDC2 causes a distinct muscular dystrophy.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. 5235, doi. 10.1093/brain/awad256
    By:
    • Mavillard, Fabiola;
    • Servian-Morilla, Emilia;
    • Dofash, Lein;
    • Rojas-Marcos, Iñigo;
    • Folland, Chiara;
    • Monahan, Gavin;
    • Gutierrez-Gutierrez, Gerardo;
    • Rivas, Eloy;
    • Hernández-Lain, Aurelio;
    • Valladares, Amador;
    • Cantero, Gloria;
    • Morales, Jose M;
    • Laing, Nigel G;
    • Paradas, Carmen;
    • Ravenscroft, Gianina;
    • Cabrera-Serrano, Macarena
    Publication type:
    Article
    25
    26

    Neuromuscular disease classification system.

    Published in:
    Journal of Biomedical Optics, 2013, v. 18, n. 6, p. 1, doi. 10.1117/1.JBO.18.6.066017
    By:
    • Sáez, Aurora;
    • Acha, Begoña;
    • Montero-Sánchez, Adoración;
    • Rivas, Eloy;
    • Escudero, Luis M.;
    • Serrano, Carmen
    Publication type:
    Article
    27

    NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay.

    Published in:
    Annals of Clinical & Translational Neurology, 2019, v. 6, n. 11, p. 2328, doi. 10.1002/acn3.50910
    By:
    • Mavillard, Fabiola;
    • Madruga‐Garrido, Marcos;
    • Rivas, Eloy;
    • Servián‐Morilla, Emilia;
    • Ávila‐Polo, Rainiero;
    • Marcos, Irene;
    • Morón, Francisco J.;
    • Paradas, Carmen;
    • Cabrera‐Serrano, Macarena
    Publication type:
    Article
    28

    Lacosamide intake during pregnancy increases the incidence of foetal malformations and symptoms associated with schizophrenia in the offspring of mice.

    Published in:
    Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64626-9
    By:
    • López-Escobar, Beatriz;
    • Fernández-Torres, Rut;
    • Vargas-López, Viviana;
    • Villar-Navarro, Mercedes;
    • Rybkina, Tatyana;
    • Rivas-Infante, Eloy;
    • Hernández-Viñas, Ayleen;
    • Álvarez del Vayo, Concepción;
    • Caro-Vega, José;
    • Sánchez-Alcázar, José A.;
    • González-Meneses, Antonio;
    • Carrión, M. Ángel;
    • Ybot-González, Patricia
    Publication type:
    Article
    29

    Correction: Gene Expression Profiling Identifies Molecular Pathways Associated with Collagen VI Deficiency and Provides Novel Therapeutic Targets.

    Published in:
    PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0128614
    By:
    • Paco, Sonia;
    • Kalko, Susana G.;
    • Jou, Cristina;
    • Rodríguez, María A.;
    • Corbera, Joan;
    • Muntoni, Francesco;
    • Feng, Lucy;
    • Rivas, Eloy;
    • Torner, Ferran;
    • Gualandi, Francesca;
    • Gomez-Foix, Anna M.;
    • Ferrer, Anna;
    • Ortez, Carlos;
    • Nascimento, Andrés;
    • Colomer, Jaume;
    • Jimenez-Mallebrera, Cecilia
    Publication type:
    Article
    30

    Gene Expression Profiling Identifies Molecular Pathways Associated with Collagen VI Deficiency and Provides Novel Therapeutic Targets.

    Published in:
    PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0077430
    By:
    • Paco, Sonia;
    • Kalko, Susana G.;
    • Jou, Cristina;
    • Rodríguez, María A.;
    • Corbera, Joan;
    • Muntoni, Francesco;
    • Feng, Lucy;
    • Rivas, Eloy;
    • Torner, Ferran;
    • Gualandi, Francesca;
    • Gomez-Foix, Anna M.;
    • Ferrer, Anna;
    • Ortez, Carlos;
    • Nascimento, Andrés;
    • Colomer, Jaume;
    • Jimenez-Mallebrera, Cecilia
    Publication type:
    Article
    31

    Late-onset thymidine kinase 2 deficiency: a review of 18 cases.

    Published in:
    2019
    By:
    • Domínguez-González, Cristina;
    • Hernández-Laín, Aurelio;
    • Rivas, Eloy;
    • Hernández-Voth, Ana;
    • Sayas Catalán, Javier;
    • Fernández-Torrón, Roberto;
    • Fuiza-Luces, Carmen;
    • García García, Jorge;
    • Morís, Germán;
    • Olivé, Montse;
    • Miralles, Frances;
    • Díaz-Manera, Jordi;
    • Caballero, Candela;
    • Méndez-Ferrer, Bosco;
    • Martí, Ramon;
    • García Arumi, Elena;
    • Badosa, María Carmen;
    • Esteban, Jesús;
    • Jimenez-Mallebrera, Cecilia;
    • Encinar, Alberto Blazquez
    Publication type:
    journal article
    32
    33
    34
    35
    36
    37
    38