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DNA methylation signature of human hippocampus in Alzheimer's disease is linked to neurogenesis.
Published in:
Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0672-7
By:
- Altuna, Miren;
- Urdánoz-Casado, Amaya;
- Sánchez-Ruiz de Gordoa, Javier;
- Zelaya, María V.;
- Labarga, Alberto;
- Lepesant, Julie M. J.;
- Roldán, Miren;
- Blanco-Luquin, Idoia;
- Perdones, Álvaro;
- Larumbe, Rosa;
- Jericó, Ivonne;
- Echavarri, Carmen;
- Méndez-López, Iván;
- Di Stefano, Luisa;
- Mendioroz, Maite
Publication type:
Article
Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain.
Published in:
2015
By:
- Dols-Icardo, Oriol;
- Nebot, Irene;
- Gorostidi, Ana;
- Ortega-Cubero, Sara;
- Hernández, Isabel;
- Rojas-García, Ricard;
- García-Redondo, Alberto;
- Povedano, Monica;
- Lladó, Albert;
- Álvarez, Victoria;
- Sánchez-Juan, Pascual;
- Pardo, Julio;
- Jericó, Ivonne;
- Vázquez-Costa, Juan;
- Sevilla, Teresa;
- Cardona, Fernando;
- Indakoechea, Begoña;
- Moreno, Fermín;
- Fernández-Torrón, Roberto;
- Muñoz-Llahuna, Laia
Publication type:
Letter
Liquid biopsy shows differences in cfDNA fragmentation pattern between AD patients and controls: Biomarkers (non‐neuroimaging) / plasma/serum/urine biomarkers.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.039748
By:
- Santamaria, Blanca Acha;
- Luquin, Idoia Blanco;
- Corroza, Jon;
- Miguel, Mikel San;
- Roldan, Miren;
- Zueco, Sara;
- Beiras, Itsaso Elizalde;
- Cabello, Carolina;
- Agudo, Maria Ángeles Garde;
- Jericó, Ivonne;
- Erro, Elena;
- Mendioroz, Maite
Publication type:
Article
Hippocampal LMNA Gene Expression is Increased in Late-Stage Alzheimer's Disease.
Published in:
International Journal of Molecular Sciences, 2019, v. 20, n. 4, p. 878, doi. 10.3390/ijms20040878
By:
- Méndez-López, Iván;
- Blanco-Luquin, Idoia;
- Sánchez-Ruiz de Gordoa, Javier;
- Urdánoz-Casado, Amaya;
- Roldán, Miren;
- Acha, Blanca;
- Echavarri, Carmen;
- Zelaya, Victoria;
- Jericó, Ivonne;
- Mendioroz, Maite
Publication type:
Article
Neuroanatomical Quantitative Proteomics Reveals Common Pathogenic Biological Routes between Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD).
Published in:
International Journal of Molecular Sciences, 2019, v. 20, n. 1, p. 4, doi. 10.3390/ijms20010004
By:
- Iridoy, Marina Oaia;
- Zubiri, Irene;
- Zelaya, María Victoria;
- Martinez, Leyre;
- Ausín, Karina;
- Lachen-Montes, Mercedes;
- Santamaría, Enrique;
- Fernandez-Irigoyen, Joaquín;
- Jericó, Ivonne
Publication type:
Article
Myasthenia gravis: Sleep quality, quality of life, and disease severity.
Published in:
Muscle & Nerve, 2012, v. 46, n. 2, p. 174, doi. 10.1002/mus.23296
By:
- De Lapiscina, Elena Hernández Martínez;
- Aguirre, María Elena Erro;
- Blanco, Teresa Ayuso;
- Pascual, Ivonne Jericó
Publication type:
Article
Evaluation of Chitotriosidase and CC-Chemokine Ligand 18 as Biomarkers of Microglia Activation in Amyotrophic Lateral Sclerosis.
Published in:
Neurodegenerative Diseases, 2018, v. 18, n. 4, p. 208, doi. 10.1159/000490920
By:
- Martinez-Merino, Leyre;
- Iridoy, Marina;
- Galbete, Arkaitz;
- Roldán, Miren;
- Rivero, Adriana;
- Acha, Blanca;
- Irún, Pilar;
- Canosa, Cecilia;
- Pocoví, Miguel;
- Mendioroz, Maite;
- Jericó, Ivonne
Publication type:
Article
Inflammatory Neuropathy Consortium base (INCbase): a protocol of a global prospective observational cohort study for the development of a prediction model for treatment response in chronic inflammatory demyelinating polyneuropathy.
Published in:
BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03903-w
By:
- Michael, Milou R.;
- Wieske, Luuk;
- Allen, Jeffrey A.;
- Lunn, Michael P.;
- Doppler, Kathrin;
- Tan, Cheng-Yin;
- Koike, Haruki;
- Markvardsen, Lars K.;
- Kapoor, Mahima;
- Hsieh, Sung-Tsang;
- Nobile-Orazio, Eduardo;
- Jacobs, Bart C.;
- Rajabally, Yusuf A.;
- Basta, Ivana;
- Ripellino, Paolo;
- Querol, Luis;
- Eftimov, Filip;
- on behalf of the INCbase Consortium;
- Gutiérrez-Gutiérrez, Gerardo;
- Pascual, Ivonne Jericó
Publication type:
Article
Drug‐refractory myasthenia gravis: Clinical characteristics, treatments, and outcome.
Published in:
Annals of Clinical & Translational Neurology, 2022, v. 9, n. 2, p. 122, doi. 10.1002/acn3.51492
By:
- Cortés‐Vicente, Elena;
- Álvarez‐Velasco, Rodrigo;
- Pla‐Junca, Francesc;
- Rojas‐Garcia, Ricard;
- Paradas, Carmen;
- Sevilla, Teresa;
- Casasnovas, Carlos;
- Gómez‐Caravaca, María Teresa;
- Pardo, Julio;
- Ramos‐Fransi, Alba;
- Pelayo‐Negro, Ana Lara;
- Gutiérrez‐Gutiérrez, Gerardo;
- Turon‐Sans, Janina;
- López de Munain, Adolfo;
- Guerrero‐Sola, Antonio;
- Jericó, Ivonne;
- Martín, María Asunción;
- Mendoza, María Dolores;
- Morís, Germán;
- Vélez‐Gómez, Beatriz
Publication type:
Article
Novel PLEKHG5 mutations in a patient with childhood‐onset lower motor neuron disease.
Published in:
Annals of Clinical & Translational Neurology, 2021, v. 8, n. 1, p. 294, doi. 10.1002/acn3.51265
By:
- Gonzalez‐Quereda, Lidia;
- Pagola, Inmaculada;
- Fuentes Prior, Pablo;
- Bernal, Sara;
- Rodriguez, Maria Jose;
- Torné, Laura;
- Salgado Garrido, Josefa;
- Gallano, Pia;
- Jericó, Ivonne
Publication type:
Article
Liquid biopsy: a new source of candidate biomarkers in amyotrophic lateral sclerosis.
Published in:
Annals of Clinical & Translational Neurology, 2018, v. 5, n. 6, p. 763, doi. 10.1002/acn3.565
By:
- Mendioroz, Maite;
- Martínez‐Merino, Leyre;
- Blanco‐Luquin, Idoia;
- Urdánoz, Amaya;
- Roldán, Miren;
- Jericó, Ivonne
Publication type:
Article
Association and linkage disequilibrium analyses of APOE polymorphisms in atherosclerosis.
Published in:
Disease Markers, 2008, v. 24, n. 2, p. 65, doi. 10.1155/2008/650410
By:
- Artieda, Marta;
- Gañán, Alberto;
- Cenarro, Ana;
- García-Otín, Ángel Luis;
- Jericó, Ivonne;
- Civeira, Fernando;
- Pocoví, Miguel
Publication type:
Article
Epidemiological study and genetic characterization of inherited muscle diseases in a northern Spanish region.
Published in:
2019
By:
- Pagola-Lorz, Inmaculada;
- Vicente, Esther;
- Ibáñez, Berta;
- Torné, Laura;
- Elizalde-Beiras, Itsaso;
- Garcia-Solaesa, Virginia;
- García, Fermín;
- Delfrade, Josu;
- Jericó, Ivonne
Publication type:
journal article
Expanding the clinical phenotypes of MT-ATP6 mutations.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 23, p. 6191
By:
- López-Gallardo, Ester;
- Emperador, Sonia;
- Solano, Abelardo;
- Llobet, Laura;
- Martín-Navarro, Antonio;
- López-Pérez, Manuel José;
- Briones, Paz;
- Pineda, Mercedes;
- Artuch, Rafael;
- Barraquer, Elena;
- Jericó, Ivonne;
- Ruiz-Pesini, Eduardo;
- Montoya, Julio
Publication type:
Article
Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease.
Published in:
European Journal of Neurology, 2023, v. 30, n. 4, p. 861, doi. 10.1111/ene.15661
By:
- Vázquez‐Costa, Juan F.;
- Borrego‐Hernández, Daniel;
- Paradas, Carmen;
- Gómez‐Caravaca, María Teresa;
- Rojas‐Garcia, Ricardo;
- Varona, Luis;
- Povedano, Mónica;
- García‐Sobrino, Tania;
- Jericó Pascual, Ivonne;
- Gutiérrez, Antonio;
- Riancho, Javier;
- Turon‐Sans, Janina;
- Assialioui, Abdelilah;
- Pérez‐Tur, Jordi;
- Sevilla, Teresa;
- Esteban Pérez, Jesús;
- García‐Redondo, Alberto;
- López, Alberto Andrés;
- Calabria, M. Dolores;
- Díaz‐Marín, Carmen
Publication type:
Article
Clinical characteristics and outcomes of thymoma‐associated myasthenia gravis.
Published in:
European Journal of Neurology, 2021, v. 28, n. 6, p. 2083, doi. 10.1111/ene.14820
By:
- Álvarez‐Velasco, Rodrigo;
- Gutiérrez‐Gutiérrez, Gerardo;
- Trujillo, Juan Carlos;
- Martínez, Elisabeth;
- Segovia, Sonia;
- Arribas‐Velasco, Marina;
- Fernández, Guillermo;
- Paradas, Carmen;
- Vélez‐Gómez, Beatriz;
- Casasnovas, Carlos;
- Nedkova, Velina;
- Guerrero‐Sola, Antonio;
- Ramos‐Fransi, Alba;
- Martínez‐Piñeiro, Alicia;
- Pardo, Julio;
- Sevilla, Teresa;
- Gómez‐Caravaca, María Teresa;
- López de Munain, Adolfo;
- Jericó, Ivonne;
- Pelayo‐Negro, Ana L.
Publication type:
Article
Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
Published in:
2019
By:
- De la Casa‐Fages, Beatriz;
- Fernández‐Eulate, Gorka;
- Gamez, Josep;
- Barahona‐Hernando, Raúl;
- Morís, Germán;
- García‐Barcina, María;
- Infante, Jon;
- Zulaica, Miren;
- Fernández‐Pelayo, Uxoa;
- Muñoz‐Oreja, Mikel;
- Urtasun, Miguel;
- Olaskoaga, Ander;
- Zelaya, Victoria;
- Jericó, Ivonne;
- Saez‐Villaverde, Raquel;
- Catalina, Irene;
- Sola, Emma;
- Martínez‐Sáez, Elena;
- Pujol, Aurora;
- Ruiz, Montserrat
Publication type:
Letter
Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism.
Published in:
2019
By:
- De la Casa‐Fages, Beatriz;
- Fernández‐Eulate, Gorka;
- Gamez, Josep;
- Barahona‐Hernando, Raúl;
- Morís, Germán;
- García‐Barcina, María;
- Infante, Jon;
- Zulaica, Miren;
- Fernández‐Pelayo, Uxoa;
- Muñoz‐Oreja, Mikel;
- Urtasun, Miguel;
- Olaskoaga, Ander;
- Zelaya, Victoria;
- Jericó, Ivonne;
- Saez‐Villaverde, Raquel;
- Catalina, Irene;
- Sola, Emma;
- Martínez‐Sáez, Elena;
- Pujol, Aurora;
- Ruiz, Montserrat
Publication type:
journal article
Exploring the Disease-Associated Microglia State in Amyotrophic Lateral Sclerosis.
Published in:
Biomedicines, 2023, v. 11, n. 11, p. 2994, doi. 10.3390/biomedicines11112994
By:
- Jauregui, Carlota;
- Blanco-Luquin, Idoia;
- Macías, Mónica;
- Roldan, Miren;
- Caballero, Cristina;
- Pagola, Inma;
- Mendioroz, Maite;
- Jericó, Ivonne
Publication type:
Article
Liquid Biopsy in Alzheimer's Disease Patients Reveals Epigenetic Changes in the PRLHR Gene.
Published in:
Cells (2073-4409), 2023, v. 12, n. 23, p. 2679, doi. 10.3390/cells12232679
By:
- Macías, Mónica;
- Acha, Blanca;
- Corroza, Jon;
- Urdánoz-Casado, Amaya;
- Roldan, Miren;
- Robles, Maitane;
- Sánchez-Ruiz de Gordoa, Javier;
- Erro, María Elena;
- Jericó, Ivonne;
- Blanco-Luquin, Idoia;
- Mendioroz, Maite
Publication type:
Article
Analysis of the C 9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide.
Published in:
Human Mutation, 2013, v. 34, n. 1, p. 79, doi. 10.1002/humu.22211
By:
- García‐Redondo, Alberto;
- Dols‐Icardo, Oriol;
- Rojas‐García, Ricard;
- Esteban‐Pérez, Jesús;
- Cordero‐Vázquez, Pilar;
- Muñoz‐Blanco, José Luis;
- Catalina, Irene;
- González‐Muñoz, Miguel;
- Varona, Luis;
- Sarasola, Esther;
- Povedano, Monica;
- Sevilla, Teresa;
- Guerrero, Antonio;
- Pardo, Julio;
- de Munain, Adolfo López;
- Márquez‐Infante, Celedonio;
- de Rivera, Francisco Javier Rodríguez;
- Pastor, Pau;
- Jericó, Ivonne;
- de Arcaya, Amaya Álvarez
Publication type:
Article
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population.
Published in:
Genes, 2019, v. 10, n. 10, p. 785, doi. 10.3390/genes10100785
By:
- Garcia-Solaesa, Virginia;
- Serrano-Lorenzo, Pablo;
- Ramos-Arroyo, Maria Antonia;
- Blázquez, Alberto;
- Pagola-Lorz, Inmaculada;
- Artigas-López, Mercè;
- Arenas, Joaquín;
- Martín, Miguel A.;
- Jericó-Pascual, Ivonne
Publication type:
Article

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