Celine Renoux

F Laboratoire De Biochimie Et Biologie Moléculaire Grand Est, Groupement Hospitalier Est
Bron, France

Last Updated: 09/26/2026

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Found 77 publications

Is it time to implement a hemorheology passport in sickle cell disease?

Is it time to implement a hemorheology passport in sickle cell disease?

Journal: Blood cells, molecules & diseases

Published: June 05, 2026

Should we longitudinally monitor blood viscosity in patients with sickle cell anemia?

Should we longitudinally monitor blood viscosity in patients with sickle cell anemia?

Journal: Blood cells, molecules & diseases

Published: April 22, 2026

Deep intronic ANK1 variants causing pseudo-exon inclusion in hereditary spherocytosis: Whole-genome sequencing and functional assessment.

Deep intronic ANK1 variants causing pseudo-exon inclusion in hereditary spherocytosis: Whole-genome sequencing and functional assessment.

Journal: British journal of haematology

Published: March 09, 2026

A Twist in the Tale: Antenatal Volvulus Following Fetal CFTR Modulator Therapy.

A Twist in the Tale: Antenatal Volvulus Following Fetal CFTR Modulator Therapy.

Journal: Pediatric pulmonology

Published: February 07, 2026

Differences in oxygen-gradient ektacytometry parameters and blood viscosity between patients with sickle cell anemia and patients with sickle cell-hemoglobin C disorder.

Differences in oxygen-gradient ektacytometry parameters and blood viscosity between patients with sickle cell anemia and patients with sickle cell-hemoglobin C disorder.

Journal: Clinical hemorheology and microcirculation

Published: July 08, 2025

Characterization of a novel SERPINA1 variant carrying two missense mutations: molecular mechanisms and functional impact.

Characterization of a novel SERPINA1 variant carrying two missense mutations: molecular mechanisms and functional impact.

Journal: Orphanet journal of rare diseases

Published: May 15, 2025

Impact of Hematocrit on Coagulation Measured by Rotational Thromboelastometry in Healthy Subjects and Patients with Polycythemia.

Impact of Hematocrit on Coagulation Measured by Rotational Thromboelastometry in Healthy Subjects and Patients with Polycythemia.

Journal: Seminars in thrombosis and hemostasis

Published: April 01, 2025

Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France.

Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France.

Journal: Blood cells, molecules & diseases

Published: March 19, 2025

Evaluation of a New Tandem Mass Spectrometry Method for Sickle Cell Disease Newborn Screening.

Evaluation of a New Tandem Mass Spectrometry Method for Sickle Cell Disease Newborn Screening.

Journal: International journal of neonatal screening

Published: September 24, 2024

Impaired microvascular function in patients with sickle cell anemia and leg ulcers improved with healing.

Impaired microvascular function in patients with sickle cell anemia and leg ulcers improved with healing.

Journal: British journal of haematology

Published: July 13, 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

Red blood cell senescence and vascular function in patients with hereditary spherocytosis with and without splenectomy.

Red blood cell senescence and vascular function in patients with hereditary spherocytosis with and without splenectomy.

Journal: British journal of haematology

Published: January 24, 2024

Showing 1-12 of 77

Last Updated: 09/26/2026