Výsledky vyhledávání - Pascual-Alonso, Ainhoa

MECP2-Related Disorders in Males Autor Pascual-Alonso, Ainhoa, Martínez-Monseny, Antonio F., Xiol, Clara, Armstrong, Judith

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Technological Improvements in the Genetic Diagnosis of Rett Syndrome Spectrum Disorders Autor Xiol, Clara, Heredia, Maria, Pascual-Alonso, Ainhoa, Oyarzabal, Alfonso, Armstrong, Judith

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Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges Autor Vidal, Silvia, Xiol, Clara, Pascual-Alonso, Ainhoa, O’Callaghan, M., Pineda, Mercè, Armstrong, Judith

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Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis Autor Vidal, Silvia, Pascual‐Alonso, Ainhoa, Rabaza‐Gairí, Marc, Gerotina, Edgar, Brandi, Nuria, Pacheco, Paola, Xiol, Clara, Pineda, Mercè, Armstrong, Judith

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X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients Autor Xiol, Clara, Vidal, Silvia, Pascual-Alonso, Ainhoa, Blasco, Laura, Brandi, Núria, Pacheco, Paola, Gerotina, Edgar, O’Callaghan, Mar, Pineda, Mercè, Armstrong, Judith

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Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy Autor Castells, Alba-Aina, Balada, Rafel, Tristán-Noguero, Alba, O’Callaghan, Mar, Cortès-Saladelafont, Elisenda, Pascual-Alonso, Ainhoa, Garcia-Cazorla, Àngels, Armstrong, Judith, Alcántara, Soledad

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Analysis of the circRNA and T-UCR populations identifies convergent pathways in mouse and human models of Rett syndrome Autor Siqueira, Edilene, Obiols-Guardia, Aida, Jorge-Torres, Olga C., Oliveira-Mateos, Cristina, Soler, Marta, Ramesh-Kumar, Deepthi, Setién, Fernando, van Rossum, Daniëlle, Pascual-Alonso, Ainhoa, Xiol, Clara, Ivan, Cristina, Shimizu, Masayoshi, Armstrong, Judith, Calin, George A., Pasterkamp, R. Jeroen, Esteller, Manel, Guil, Sonia

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