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Ejhaem|October 6, 2025
Insights Into Hemoglobinopathies in Spain: A Comprehensive ReviewJoan-Lluis Vives CorronsJournal of Clinical Medicine|June 19, 2024
Understanding Rare Anemias: Emerging Frontiers for Diagnosis and TreatmentJoan-Lluis Vives CorronsActa Bio-Medica : Atenei Parmensis|March 8, 2021
Rare anemias in adolescentsJoan Lluis Vives-Corrons, Elena KrishnevskayaActa Bio-Medica : Atenei Parmensis|May 19, 2020
Rare Anaemias, Sickle-Cell Disease and COVID-19Joan-Lluis Vives Corrons, Vincenzo De SanctisBlood Cells, Molecules & Diseases|January 29, 2022
Haemoglobin Bristol-Alesha in a child with non-spherocytic severe haemolytic anaemia and marked anisochromic poikilocytosis with basophilic stippling and amorphous intracellular contentJoan-Lluis Vives Corrons, Barbara J BainActa Bio-Medica : Atenei Parmensis|February 2, 2021
The Multifacets of COVID-19 in Adult Patients: A Concise Clinical Review on Pulmonary and Extrapulmonary Manifestations for Healthcare PhysiciansDuran Canatan, Joan Lluis Vives Corrons, Vincenzo De SanctisThescientificworldjournal|April 12, 2013
The impact of migrations on the health services for rare diseases in Europe: the example of haemoglobin disordersMichalis Angastiniotis, Joan-Lluis Vives Corrons, Elpidoforos S Soteriades, et al.International Journal of Hematology|October 19, 2020
Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometryJoan-Lluis Vives-Corrons, Elena Krishnevskaya, Ines Hernandez Rodriguez, et al.Hemoglobin|August 7, 2009
Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disordersMaria del Mar Mañú Pereira, Anna Cabot Dalmau, Joan-Lluis Vives CorronsBiochimica Et Biophysica Acta|June 14, 2005
Glucose phosphate isomerase deficiency: enzymatic and familial characterization of Arg346His mutationAda Repiso, Baldomero Oliva, Joan-Lluis Vives Corrons, et al.Pageof 4