María-Angustias Molina-Arrebola

7PUBLICATIONS
4CO-AUTHORS
Social epidemiologyGene expression (incl. microarray and other genome-wide approaches)Respiratory diseasesSystems physiologyCardiovascular medicine and haematology not elsewhere classified
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Publications (7)

|Aug 04, 2026
Evolution of hemoglobinopathy diagnosis over 30 years in southern Spain: impact of migration and laboratory screening strategies.

|Jun 02, 2026
Beta-Thalassemia in Spain: Results From the National Thalassemia Registry and Molecular Analysis of Patients With Transfusion-Dependent Thalassemia.

|Apr 22, 2026
High-performance liquid chromatography screening reveals HbS/β+-thalassemia double heterozygosity as a pediatric muscular dystrophy mimic.

|Jul 28, 2025
Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrinLELY in Trans.

María-Angustias Molina-Arrebola, Barbara J Bain

|Jul 09, 2025
Not All Hereditary Iron Overload Is Hemochromatosis: A Case of Hereditary Xerocytosis Unmasked by Blood Smear Morphology.

María-Angustias Molina-Arrebola, Barbara J Bain

|Jun 18, 2025
Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil.

María-Angustias Molina-Arrebola, Barbara J Bain

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Frequent Collaborators

4 joint publications

Barbara J Bain

1 joint publications

Paloma Ropero

1 joint publications

María Menor

1 joint publications

Jesús María Hernández-Rivas