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Lídia Romero‐Cortadellas

Observed names: L. Romero-Cortadellas, Lídia Romero-Cortadellas, Romero Cortadellas, Lídia
ORCID: 0000-0003-1080-3774
Observed ORCID: 0000-0003-1080-3774
OpenAlex ID: A5064841944
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II
2023 · Melina Mara Musri, Veronica Venturi, et al. · International Journal of Molecular Sciences · 11
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Absence of p.R50X Pygm read-through in McArdle disease cellular models
2019 · Guillermo Tarrasó, Alberto Real-Martinez, et al. · Disease Models & Mechanisms · 10
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Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III
2022 · Gonzalo Hernández, Lídia Romero-Cortadellas, et al. · Haematologica · 9
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Haemochromatosis patients' research priorities: Towards an improved quality of life
2023 · Lídia Romero‐Cortadellas, Veronica Venturi, et al. · Health Expectations · 8
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New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation
2022 · Lídia Romero-Cortadellas, Gonzalo Hernández, et al. · International Journal of Molecular Sciences · 8
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Autosomal Recessive Congenital Dyserythropoietic Anemia Type III Is Caused By Mutations in the Centralspindlin RACGAP1 Component
2021 · Lídia Romero-Cortadellas, Gonzalo Hernández, et al. · Blood · 6
Novel transferrin gene mutations in four new cases of congenital Atransferrinaemia: Functional and diagnostic pathogenicity despite negative bioinformatics
2024 · Lídia Romero‐Cortadellas, Xènia Ferrer‐Cortès, et al. · British Journal of Haematology · 1
S274: a Novel Subtype of Anemia Caused by Mutations in Tfrc Gene
2022 · S. Colucci, V. Venturi, et al. · HemaSphere · 1
P1496: Transferrin Non-coding Variants Cause Mrna Destabilisation in Congenital Hypotransferrinemia
2023 · Xenia Ferrer, Lídia Romero-Cortadellas, et al. · HemaSphere
P1475: Mutations in the Gap Domain of Racgap1 Cause Developmental and Erythroid Defects in Zebrafish
2023 · Lídia Romero-Cortadellas, Aitor Bañón, et al. · HemaSphere
P1431: Molecular Characterization and Lentiviral Correction of in Vitro Erythropoieis in Patients With a Novel Recessive Congenital Dyserythropoietic Anemia Type Iii (cda Type Iiib).
2022 · G. Hernández, L. Romero-Cortadellas, et al. · HemaSphere
Works count: 12
Citation count: 54
H-index: 6
I10-index: 2
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