Catherine Badens

Marseille, 13385, France

Last Updated: 09/26/2026

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Found 93 publications

Chasing uncertain significance in PIEZO1 variants.

Chasing uncertain significance in PIEZO1 variants.

Journal: Blood

Published: July 09, 2026

Transition from Pediatric to Adult Care in Patients with Transfusion-Dependent Beta-Thalassemia in France: A National Study Concerning a Rare Disease.

Transition from Pediatric to Adult Care in Patients with Transfusion-Dependent Beta-Thalassemia in France: A National Study Concerning a Rare Disease.

Journal: Journal of clinical medicine

Published: January 22, 2026

Base editing of β0-thalassemia mutations as a therapeutic strategy for severe β-hemoglobinopathies.

Base editing of β0-thalassemia mutations as a therapeutic strategy for severe β-hemoglobinopathies.

Journal: Science translational medicine

Published: November 26, 2025

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study.

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study.

Journal: HemaSphere

Published: November 26, 2025

Genetics and cancer-related Laminopathies: Involvement of Lamins and Lamin-Chromatin Interactions.

Genetics and cancer-related Laminopathies: Involvement of Lamins and Lamin-Chromatin Interactions.

Journal: Sub-cellular biochemistry

Published: September 26, 2025

A new unstable haemoglobin, Hb Alger, causes a transfusion-dependent anaemia in early childhood.

A new unstable haemoglobin, Hb Alger, causes a transfusion-dependent anaemia in early childhood.

Journal: British journal of haematology

Published: April 25, 2025

Homozygous loss of function variant in LMNB2 gene causes major brain malformation and perinatal death.

Homozygous loss of function variant in LMNB2 gene causes major brain malformation and perinatal death.

Journal: Journal of medical genetics

Published: December 04, 2024

Rare ZMPSTE24 variants increase risk of hypertriglyceridemia and metabolic syndrome.

Rare ZMPSTE24 variants increase risk of hypertriglyceridemia and metabolic syndrome.

Journal: European journal of endocrinology

Published: October 09, 2024

A novel red blood cell deformability biomarker is associated with hemolysis and vaso-occlusive crises in sickle cell disease.

A novel red blood cell deformability biomarker is associated with hemolysis and vaso-occlusive crises in sickle cell disease.

Journal: Scientific reports

Published: August 10, 2024

Intragenic deletions in SPTB are associated with hereditary spherocytosis: Series of 12 cases.

Intragenic deletions in SPTB are associated with hereditary spherocytosis: Series of 12 cases.

Journal: British journal of haematology

Published: June 05, 2024

Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.

Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.

Journal: Haematologica

Published: September 20, 2023

Health status and quality of life in β-thalassemia adults in Marseille, France

Health status and quality of life in β-thalassemia adults in Marseille, France

Journal: La Revue de medecine interne

Published: July 08, 2023

Showing 1-12 of 93

Last Updated: 09/26/2026