Lídia Romero-Cortadellas

5PUBLICATIONS
15CO-AUTHORS
Nanotoxicology, health and safetyRespiratory diseasesCardiovascular medicine and haematology not elsewhere classifiedMedical mycologyCardiology (incl. cardiovascular diseases)
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Publications (5)

|Jul 31, 2024
Novel transferrin gene mutations in four new cases of congenital Atransferrinaemia: Functional and diagnostic pathogenicity despite negative bioinformatics.

Lídia Romero-Cortadellas, Xènia Ferrer-Cortès, Laura Calvo-López

|Jul 28, 2023
Haemochromatosis patients' research priorities: Towards an improved quality of life.

Lídia Romero-Cortadellas, Veronica Venturi, Juan Carlos Martín-Sánchez

|Jun 28, 2023
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II.

Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès

|Apr 23, 2022
New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation.

Lídia Romero-Cortadellas, Gonzalo Hernández, Xènia Ferrer-Cortès

|Dec 19, 2019
Absence of p.R50X Pygm read-through in McArdle disease cellular models.

Guillermo Tarrasó, Alberto Real-Martinez, Marta Parés

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Frequent Collaborators

3 joint publications

Mayka Sánchez

2 joint publications

Gonzalo Hernández

2 joint publications

Xènia Ferrer-Cortès

1 joint publications

Laura Moya