Lídia Romero-Cortadellas

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Venues

International journal of molecular sciences

Disease models & mechanisms

British journal of haematology

Health expectations : an international journal of public participation in health care and health policy

Universitat Internacional de Catalunya Facultat de Medicina i Ciències de la Salut

Universitat Autònoma de Barcelona Facultat de Biociències (MSC)

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

Affiliation History

Universitat Internacional de Catalunya Facultat de Medicina i Ciències de la Salut Jan 13 2020

Spain

PhD Student; :: Basic Sciences, Group in Iron metabolism, regulation and diseases

Vall d'Hebron Research Institute Sep 01 2018 - Jun 25 2019

Spain

Academic practices. Study of the readthrough therapy in an in vitro model of McArdle disease :: Gene and Cell Therapy Group

Banc de Sang i Teixits Jul 01 2017 - Sep 01 2017

Spain

Academic practices. Identification of irregular erythrocyte antibodies in patient-derived samples :: Red series laboratory; immunohematology area

Universitat Autònoma de Barcelona Facultat de Medicina

Spain

Informatic support in the International Project "Digital Embryology Consortium" :: Anatomy Unit

Banc de Sang i Teixits Jul 01 2013 - Jul 31 2013

Spain

Support for blood donation and transfusoin

Education History

Universitat Autònoma de Barcelona Facultat de Biociències

Spain

MSC

Universitat Autònoma de Barcelona Facultat de Biociències

Spain

BSC

Publications

Lídia Romero-Cortadellas, Xènia Ferrer-Cortès, Laura Calvo-López, Mireia Olivella, Anna Barqué, Christina Diaz de Heredia, Katja Moser, Ilona Kleine Budde, Mayka Sanchez
Novel transferrin gene mutations in four new cases of congenital Atransferrinaemia: Functional and diagnostic pathogenicity despite negative bioinformatics. British journal of haematology (2024)
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernandez, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María Del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. International journal of molecular sciences 24 (12) (2023)
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernandez, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María Del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. International journal of molecular sciences 24 (12) (2023)
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernandez, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María Del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. International journal of molecular sciences 24 (12) (2023)
Lídia Romero-Cortadellas, Veronica Venturi, Juan Carlos Martín-Sánchez, Ketil Toska, Dianne Prince, Barbara Butzeck, Graça Porto, Nils Thorm Milman, Hi/Efaph Survey Committee, Mayka Sánchez
Haemochromatosis patients' research priorities: Towards an improved quality of life. Health expectations : an international journal of public participation in health care and health policy (2023)
Lídia Romero-Cortadellas, Gonzalo Hernandez, Xènia Ferrer-Cortès, Laura Zalba-Jadraque, Jose-Luis Fuster, Mar Bermúdez-Cortés, Ana María Galera, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation. International journal of molecular sciences 23 (8) (2022)
Guillermo Tarrasó, Alberto Real-Martinez, Marta Parés, Lídia Romero-Cortadellas, Laura Puigros, Laura Moya-Borrego, Noemí de Luna, Astrid Brull, Miguel Angel Martin, Joaquin Arenas, Alejandro Lucia, Antoni L Andreu, Jordi Barquinero, John Vissing, Thomas O Krag, Tomàs Pinós
Absence of p.R50X Pygm read-through in McArdle disease cellular models. Disease models & mechanisms 13 (1) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Lídia Romero-Cortadellas