Showing 1 - 16 results of 16 for search 'Ariadna Ayerza‐Casas', query time: 0.05s
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Síndrome de tortuosidad arterial en un paciente pediátrico by Daniel Palanca Arias, Ariadna Ayerza Casas, Cristina Gutiérrez Alonso, Lorenzo Jiménez Montañés
Published 2020-02-01
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Atrial flutter without structural heart disease in pediatrics: a retrospective review of cases in the Hospital Infantil Miguel Servet, Zaragoza, Spain by Tamara Moliner-Morón, Rebeca Santiago-Cortés, Ariadna Ayerza-Casas, Marcos Clavero-Adell, Lorenzo Jiménez-Montañés, Daniel Palanca-Arias
Published 2022-01-01
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Arterial tortuosity syndrome (variants in SLC2A10 gene) in two pediatric patients in the same city of Spain: a case report by Daniel Palanca Arias, Ariadna Ayerza Casas, Marcos Clavero Adell, Cristina Gutiérrez Alonso, Marta López Ramón, Lorenzo Jiménez Montañés, Victoria Estaben Boldova, Silvia Izquierdo-Álvarez
Published 2022-09-01
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Impact of Suspected Preterm Labor during Pregnancy on Cardiometabolic Profile and Neurodevelopment during Childhood: A Prospective Cohort Study Protocol by Jesús González, Marina Vilella, Sonia Ruiz, Iris Iglesia, Marcos Clavero-Adell, Ariadna Ayerza-Casas, Angel Matute-Llorente, Daniel Oros, Jose Antonio Casajús, Victoria Pueyo, Gerardo Rodriguez, Cristina Paules
Published 2023-03-01
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Heart Disease Characterization and Myocardial Strain Analysis in Patients with <i>PACS1</i> Neurodevelopmental Disorder by Ana Latorre-Pellicer, Laura Trujillano, Julia del Rincón, Mónica Peña-Marco, Marta Gil-Salvador, Cristina Lucia-Campos, María Arnedo, Beatriz Puisac, Feliciano J. Ramos, Ariadna Ayerza-Casas, Juan Pié
Published 2023-06-01
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Things are not always what they seem: From Cornelia de Lange to KBG phenotype in a girl with genetic variants in NIPBL and ANKRD11 by Ana Latorre‐Pellicer, Ángela Ascaso, Cristina Lucia‐Campos, Marta Gil‐Salvador, María Arnedo, Rebeca Antoñanzas, Ariadna Ayerza‐Casas, Iñigo Marcos‐Alcalde, Paulino Gómez‐Puertas, Feliciano J. Ramos, Juan Pié, Beatriz Puisac
Published 2021-11-01
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Molecular Basis of the Schuurs–Hoeijmakers Syndrome: What We Know about the Gene and the PACS-1 Protein and Novel Therapeutic Approaches by María Arnedo, Ángela Ascaso, Ana Latorre-Pellicer, Cristina Lucia-Campos, Marta Gil-Salvador, Ariadna Ayerza-Casas, María Jesús Pablo, Paulino Gómez-Puertas, Feliciano J. Ramos, Gloria Bueno-Lozano, Juan Pié, Beatriz Puisac
Published 2022-08-01
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Targeted Gene Sequencing, Bone Health, and Body Composition in Cornelia de Lange Syndrome by Ángel Matute-Llorente, Ángela Ascaso, Ana Latorre-Pellicer, Beatriz Puisac, Laura Trujillano, Elena Llorente, Juan José Puente-Lanzarote, Ariadna Ayerza-Casas, María Arnedo, Luis A. Moreno, Feliciano Ramos, Juan Pié, José A. Casajus, Gloria Bueno-Lozano
Published 2021-01-01
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Clinical relevance of postzygotic mosaicism in Cornelia de Lange syndrome and purifying selection of NIPBL variants in blood by Ana Latorre-Pellicer, Marta Gil-Salvador, Ilaria Parenti, Cristina Lucia-Campos, Laura Trujillano, Iñigo Marcos-Alcalde, María Arnedo, Ángela Ascaso, Ariadna Ayerza-Casas, Rebeca Antoñanzas-Pérez, Cristina Gervasini, Maria Piccione, Milena Mariani, Axel Weber, Deniz Kanber, Alma Kuechler, Martin Munteanu, Katharina Khuller, Gloria Bueno-Lozano, Beatriz Puisac, Paulino Gómez-Puertas, Angelo Selicorni, Frank J. Kaiser, Feliciano J. Ramos, Juan Pié
Published 2021-07-01
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