Ana Argudo‐Ramírez

First Universal Newborn Screening Program for Severe Combined Immunodeficiency in Europe. Two-Years' Experience in Catalonia (Spain)

Ana Argudo‐Ramírez, Andrea Martín-Nalda, José Luís Marín-Soria et al. · Frontiers in Immunology · 2019 · 49 citations · Full text

Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns

Sonia Pajares, José Antonio Arranz, Aída Ormazábal et al. · Orphanet Journal of Rare Diseases · 2021 · 29 citations · Full text

Newborn Screening for SCID: Experience in Spain (Catalonia)

Ana Argudo‐Ramírez, Andrea Martín-Nalda, José Manuel González de Aledo‐Castillo et al. · International Journal of Neonatal Screening · 2021 · 16 citations · Full text

Immunohematology, Neonatology, Immunodeficiencies +23

Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years’ experience in Catalonia (Spain)

Andrea Martín-Nalda, Anna M. Cueto‐González, Ana Argudo‐Ramírez et al. · Molecular Genetics & Genomic Medicine · 2019 · 14 citations · Full text

An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations

Sonia Pajares, Rosa María López, Laura Gort et al. · Molecular Genetics and Metabolism Reports · 2020 · 14 citations · Full text