Paloma Ropero

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 53 publications

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

Journal: Hemoglobin
Published: September 03, 2026

Digital PCR-based non-invasive prenatal diagnosis should be considered in the evolving diagnostic pathway for sickle cell disease.

Digital PCR-based non-invasive prenatal diagnosis should be considered in the evolving diagnostic pathway for sickle cell disease.

Journal: HemaSphere
Published: June 17, 2026

First Case of Hb City of Hope (HBB: c.208G > A) in Andalusia. A Molecular Update of β-Thalassemia in Southwestern Spain (Huelva Province).

First Case of Hb City of Hope (HBB: c.208G > A) in Andalusia. A Molecular Update of β-Thalassemia in Southwestern Spain (Huelva Province).

Journal: Hemoglobin
Published: March 03, 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

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

An HBB Intron 1 Variant (c.92 + 9C > T) Suggestive of β-Thalassemia Trait.

An HBB Intron 1 Variant (c.92 + 9C > T) Suggestive of β-Thalassemia Trait.

Journal: Hemoglobin
Published: August 11, 2025

Molecular Characterization of Three Novel Large Deletions Causing α0-Thalassemia.

Molecular Characterization of Three Novel Large Deletions Causing α0-Thalassemia.

Journal: International journal of molecular sciences
Published: August 01, 2025

Importance of the 3'UTR region in globin synthesis: identification of two novel HBA1 mutations causing α-Thalassemia.

Importance of the 3'UTR region in globin synthesis: identification of two novel HBA1 mutations causing α-Thalassemia.

Journal: Annals of hematology
Published: July 04, 2025

Structural and clinical characterization of Hb Móstoles (HBA2:c.176A>G; p.His59Arg): a new unstable alpha-globin variant with thalassemic features.

Structural and clinical characterization of Hb Móstoles (HBA2:c.176A>G; p.His59Arg): a new unstable alpha-globin variant with thalassemic features.

Journal: American journal of blood research
Published: March 11, 2025

Phenotype of sickle cell disease. Correlation of haplotypes and polymorphisms in cluster β, BCL11A, and HBS1L-MYB. Pilot study.

Phenotype of sickle cell disease. Correlation of haplotypes and polymorphisms in cluster β, BCL11A, and HBS1L-MYB. Pilot study.

Journal: Frontiers in medicine
Published: November 30, 2023

β-Thalassemia Intermedia: Interaction of α-Globin Gene Triplication With β-thalassemia Heterozygous in Spain.

β-Thalassemia Intermedia: Interaction of α-Globin Gene Triplication With β-thalassemia Heterozygous in Spain.

Journal: Frontiers in medicine
Published: January 31, 2022
Showing 1-12 of 53

Last Updated: 09/26/2026