Elisabeth Castellanos

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Topics

Top Venues

Journal of medical genetics

Archives of toxicology

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

Publications

Alberto F Maroto, Mireia Borrajo, Silvia Prades, Àngela Callejo, Emilio Amilibia, Marta Pérez-Grau, Francesc Roca-Ribas, Elisabeth Castellanos, Alejandro Barrallo-Gimeno, Jordi Llorens
The vestibular calyceal junction is dismantled following subchronic streptomycin in rats and sensory epithelium stress in humans. Archives of toxicology (2023)
Belen Garcia, Nuria Catasus, Andrea Ros, Inma Rosas, Alejandro Negro, Mercedes Guerrero-Murillo, Ana Maria Valero, Anna Duat-Rodriguez, Juan Luis Becerra, Sandra Bonache, Conxi Lazaro Garcia, Carmina Comas, Isabel Bielsa, Eduard Serra, Concepción Hernández-Chico, Yolanda Martin, Elisabeth Castellanos, Ignacio Blanco
Neurofibromatosis type 1 families with first-degree relatives harbouring distinct <i>NF1</i> pathogenic variants. Genetic counselling and familial diagnosis: what should be offered? Journal of medical genetics 59 (10) (2022)
Núria Catasús, Belen Garcia, Iván Galván-Femenía, Adrià Plana, Alejandro Negro, Inma Rosas, Andrea Ros, Emilio Amilibia, Juan Luis Becerra, Cristina Hostalot, Francesc Rocaribas, Isabel Bielsa, Conxi Lazaro Garcia, Rafael de Cid, Eduard Serra, Ignacio Blanco, Elisabeth Castellanos, null null
Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic component. Journal of medical genetics (2021)
Arkadiusz Piotrowski, Magdalena Koczkowska, Andrzej B Poplawski, Rafał Bartoszewski, Jarosław Króliczewski, Alina Mieczkowska, Alicia Gomes, Michael R Crowley, David K Crossman, Yunjia Chen, Ping Lao, Eduard Serra, Meritxell C Llach, Elisabeth Castellanos, Ludwine M Messiaen
Targeted massively parallel sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas: An analysis of 51 individuals in a single-center experience. Human mutation (2021)