檢索結果 - Pascual-Alonso, Ainhoa

MECP2-Related Disorders in Males 由 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 由 Xiol, Clara, Heredia, Maria, Pascual-Alonso, Ainhoa, Oyarzabal, Alfonso, Armstrong, Judith

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Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges 由 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 由 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 由 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 由 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 由 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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