Francisco J Del Castillo

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Duchenne Muscular Dystrophy

Ejection Fraction

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

María Domínguez-Ruiz, Silvia Murillo-Cuesta, Julio Contreras, Marta Cantero, Gema Garrido, Belén Martín-Bernardo, Elena Gómez-Rosas, Almudena Fernández, Francisco J Del Castillo, Lluís Montoliu, Isabel Varela-Nieto, Ignacio Del Castillo
A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study. BMC genomics 25 (1) (2024)
María Domínguez-Ruiz, Silvia Murillo-Cuesta, Julio Contreras, Marta Cantero, Gema Garrido, Belén Martín-Bernardo, Elena Gómez-Rosas, Almudena Fernández, Francisco J Del Castillo, Lluís Montoliu, Isabel Varela-Nieto, Ignacio Del Castillo
A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study. BMC genomics 25 (1) (2024)
María Domínguez-Ruiz, Silvia Murillo-Cuesta, Julio Contreras, Marta Cantero, Gema Garrido, Belén Martín-Bernardo, Elena Gómez-Rosas, Almudena Fernández, Francisco J Del Castillo, Lluís Montoliu, Isabel Varela-Nieto, Ignacio Del Castillo
A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study. BMC genomics 25 (1) (2024)
María Domínguez-Ruiz, Silvia Murillo-Cuesta, Julio Contreras, Marta Cantero, Gema Garrido, Belén Martín-Bernardo, Elena Gómez-Rosas, Almudena Fernández, Francisco J Del Castillo, Lluís Montoliu, Isabel Varela-Nieto, Ignacio Del Castillo
A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study. BMC genomics 25 (1) (2024)
María Domínguez-Ruiz, Silvia Murillo-Cuesta, Julio Contreras, Marta Cantero, Gema Garrido, Belén Martín-Bernardo, Elena Gómez-Rosas, Almudena Fernández, Francisco J Del Castillo, Lluís Montoliu, Isabel Varela-Nieto, Ignacio Del Castillo
A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study. BMC genomics 25 (1) (2024)
María Domínguez-Ruiz, Laura Ruiz-Palmero, Paula I Buonfiglio, Irene García-Vaquero, Elena Gómez-Rosas, Marina Goñi, Manuela Villamar, Matias Morín, Miguel Angel Moreno-Pelayo, Ana Belén Elgoyhen, Francisco J Del Castillo, Viviana Dalamón, Ignacio Del Castillo
Novel Pathogenic Variants in the Gene Encoding Stereocilin ( STRC ) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects. Biomedicines 11 (11) (2023)
Sinziana Stanescu, Patricia Correcher, Francisco J Del Castillo, Olga Alonso Luengo, Luis Maria Arto Millan, Amaya Belanger Quintana, Maria Camprodon Gómez, Lydia Diez Langhetée, Oscar Garcia Campos, Ana Matas-García, Jimena Perez-Moreno, Barbara Rubio Gribble, Nuria Visa-Reñé, Pilar Giraldo, Mar O'Callaghan Gordo
Clinical Outcomes of Patients with Chronic Neuropathic Form of Gaucher Disease in the Spanish Real-World Setting: A Retrospective Study. Biomedicines 11 (10) (2023)
Gloria Muñoz, David García-Seisdedos, Crina Ciubotariu, Miguel Piris-Villaespesa, Marta Gandía, Fernando Martín-Moro, Luis G Gutiérrez-Solana, Marta Morado, Javier López-Jiménez, Antonio Sánchez-Herranz, Jesús Villarrubia, Francisco J Del Castillo
Early detection of lysosomal diseases by screening of cases of idiopathic splenomegaly and/or thrombocytopenia with a next-generation sequencing gene panel. JIMD reports 51 (1) (2019)