Hasil Pencarian - Ariadna AyerzaCasas
- Menampilkan 1 - 16 hasil dari 16
-
1
-
2
-
3
Síndrome de tortuosidad arterial en un paciente pediátrico oleh Daniel Palanca Arias, Ariadna Ayerza Casas, Cristina Gutiérrez Alonso, Lorenzo Jiménez Montañés
Diterbitkan 2020-02-01Dapatkan teks lengkap
Artikel -
4
-
5
-
6
Atrial flutter without structural heart disease in pediatrics: a retrospective review of cases in the Hospital Infantil Miguel Servet, Zaragoza, Spain oleh Tamara Moliner-Morón, Rebeca Santiago-Cortés, Ariadna Ayerza-Casas, Marcos Clavero-Adell, Lorenzo Jiménez-Montañés, Daniel Palanca-Arias
Diterbitkan 2022-01-01Dapatkan teks lengkap
Artikel -
7
-
8
-
9
Evolución del riesgo cardiometabólico en pacientes supervivientes de leucemia aguda infantil oleh Elena Guadalupe Corella Aznar, Ariadna Ayerza Casas, Pilar Samper Villagrasa, Carmen Rodríguez Vigil, Lorenzo Jiménez Montañés, Carlota Calvo Escribano, José Ignacio Labarta Aizpun
Dapatkan teks lengkap
Artikel -
10
Arterial tortuosity syndrome (variants in SLC2A10 gene) in two pediatric patients in the same city of Spain: a case report oleh Daniel Palanca Arias, Ariadna Ayerza Casas, Marcos Clavero Adell, Cristina Gutiérrez Alonso, Marta López Ramón, Lorenzo Jiménez Montañés, Victoria Estaben Boldova, Silvia Izquierdo-Álvarez
Diterbitkan 2022-09-01Dapatkan teks lengkap
Artikel -
11
Impact of Suspected Preterm Labor during Pregnancy on Cardiometabolic Profile and Neurodevelopment during Childhood: A Prospective Cohort Study Protocol oleh 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
Diterbitkan 2023-03-01Dapatkan teks lengkap
Artikel -
12
Things are not always what they seem: From Cornelia de Lange to KBG phenotype in a girl with genetic variants in NIPBL and ANKRD11 oleh 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
Diterbitkan 2021-11-01Dapatkan teks lengkap
Artikel -
13
Molecular Basis of the Schuurs–Hoeijmakers Syndrome: What We Know about the Gene and the PACS-1 Protein and Novel Therapeutic Approaches oleh 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
Diterbitkan 2022-08-01Dapatkan teks lengkap
Artikel -
14
Targeted Gene Sequencing, Bone Health, and Body Composition in Cornelia de Lange Syndrome oleh 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
Diterbitkan 2021-01-01Dapatkan teks lengkap
Artikel -
15
Endocrine Evaluation and Homeostatic Model Assessment in Patients with Cornelia de Lange Syndrome oleh Ángela Ascaso, Ana Latorre-Pellicer, Beatriz Puisac, Laura Trujillano, María Arnedo, Ilaria Parenti, Elena Llorente, Juan José Puente-Lanzarote, Ángel Matute-Llorente, Ariadna Ayerza-Casas, Frank J. Kaiser, Feliciano J. Ramos, Juan Pié Juste, Gloria Bueno-Lozano
Diterbitkan 2024-06-01Dapatkan teks lengkap
Artikel -
16
Clinical relevance of postzygotic mosaicism in Cornelia de Lange syndrome and purifying selection of NIPBL variants in blood oleh 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
Diterbitkan 2021-07-01Dapatkan teks lengkap
Artikel