Valle Recasens

Zaragoza, AR, Spain

Last Updated: 09/26/2026

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Found 27 publications

Autoimmune cytopenias as an early manifestation of common variable immunodeficiency.

Autoimmune cytopenias as an early manifestation of common variable immunodeficiency.

Journal: Medicina clinica

Published: June 03, 2026

Neurological Complications in Sickle Cell Disease: Clinical, Analytical and Radiological Correlations in a Multicentre Cohort.

Neurological Complications in Sickle Cell Disease: Clinical, Analytical and Radiological Correlations in a Multicentre Cohort.

Journal: Hemoglobin

Published: March 03, 2026

Implementation of third-generation digital PCR for non-invasive prenatal diagnosis of sickle cell disease and early detection. Pilot study.

Implementation of third-generation digital PCR for non-invasive prenatal diagnosis of sickle cell disease and early detection. Pilot study.

Journal: Frontiers in medicine

Published: February 23, 2026

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

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

Journal: Journal of clinical laboratory analysis

Published: January 19, 2026

Diagnostic reassessment in myeloproliferative neoplasms: the value of functional iron parameters and JAK2 allelic burden.

Diagnostic reassessment in myeloproliferative neoplasms: the value of functional iron parameters and JAK2 allelic burden.

Journal: Annals of hematology

Published: September 10, 2025

Unlocking Rare Diagnoses: The Essential Role of Molecular Techniques in Hemoglobin Agrinio. A Case Report.

Unlocking Rare Diagnoses: The Essential Role of Molecular Techniques in Hemoglobin Agrinio. A Case Report.

Journal: European journal of haematology

Published: August 12, 2025

Unlocking Rare Diagnoses: The Essential Role of Molecular Techniques in Hemoglobin Agrinio. A Case Report.

Unlocking Rare Diagnoses: The Essential Role of Molecular Techniques in Hemoglobin Agrinio. A Case Report.

Journal: European journal of haematology

Published: August 12, 2025

Rare onset of congenital thrombotic thrombocytopenic purpura during pregnancy: A novel ADAMTS13 gene variant.

Rare onset of congenital thrombotic thrombocytopenic purpura during pregnancy: A novel ADAMTS13 gene variant.

Journal: Transfusion

Published: December 28, 2024

Transfusion independence after lenalidomide discontinuation in patients with del(5q) myelodysplastic neoplasm: a HARMONY Alliance study.

Transfusion independence after lenalidomide discontinuation in patients with del(5q) myelodysplastic neoplasm: a HARMONY Alliance study.

Journal: Leukemia

Published: April 12, 2024

Haemoglobinopathies and other rare anemias in Spain: ten years of a nationwide registry (REHem-AR).

Haemoglobinopathies and other rare anemias in Spain: ten years of a nationwide registry (REHem-AR).

Journal: Annals of hematology

Published: February 16, 2024

Does size matter? Two new deletions in the HBB gene cause β0-thalassemia.

Does size matter? Two new deletions in the HBB gene cause β0-thalassemia.

Journal: Annals of hematology

Published: January 28, 2022

CYB5R3 homozygous pathogenic variant as a rare cause of cyanosis in the newborn.

CYB5R3 homozygous pathogenic variant as a rare cause of cyanosis in the newborn.

Journal: Clinical biochemistry

Published: September 16, 2021

Showing 1-12 of 27

Last Updated: 09/26/2026