Severine Cunat

Montpellier, France

Last Updated: 09/26/2026

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Found 17 publications

French-Speaking Network of Pharmacogenetics (RNPGx) Recommendations for Gene Panel Analysis Through Genotyping or Sequencing in Pharmacogenetics.

French-Speaking Network of Pharmacogenetics (RNPGx) Recommendations for Gene Panel Analysis Through Genotyping or Sequencing in Pharmacogenetics.

Journal: Fundamental & clinical pharmacology

Published: June 23, 2025

Hereditary Combined Deficiency of the Vitamin K-Dependent Coagulation Factors.

Hereditary Combined Deficiency of the Vitamin K-Dependent Coagulation Factors.

Journal: Hamostaseologie

Published: June 20, 2025

Iron overload in hereditary spherocytosis: Are genetic factors the cause?

Iron overload in hereditary spherocytosis: Are genetic factors the cause?

Journal: British journal of haematology

Published: August 08, 2024

French-Speaking Network of Pharmacogenetics (RNPGx) Recommendations for Clinical Use of Mavacamten.

French-Speaking Network of Pharmacogenetics (RNPGx) Recommendations for Clinical Use of Mavacamten.

Journal: Clinical pharmacology and therapeutics

Published: July 31, 2024

A newly identified ferritin L-subunit variant results in increased proteasomal subunit degradation, impaired complex assembly, and severe hypoferritinemia.

A newly identified ferritin L-subunit variant results in increased proteasomal subunit degradation, impaired complex assembly, and severe hypoferritinemia.

Journal: American journal of hematology

Published: May 16, 2023

A case of inter-assay HbA1c discrepancy due to Hemoglobin G-Copenhagen.

A case of inter-assay HbA1c discrepancy due to Hemoglobin G-Copenhagen.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 23, 2022

GGCX-related congenital combined vitamin K-dependent clotting factors deficiency-1: Description of a fetus with chondrodysplasia punctata.

GGCX-related congenital combined vitamin K-dependent clotting factors deficiency-1: Description of a fetus with chondrodysplasia punctata.

Journal: American journal of medical genetics. Part A

Published: March 03, 2021

Serious Ivermectin Toxicity and Human ABCB1 Nonsense Mutations.

Serious Ivermectin Toxicity and Human ABCB1 Nonsense Mutations.

Journal: The New England journal of medicine

Published: August 20, 2020

A simple clinical score to promote and enhance ferroportin disease screening.

A simple clinical score to promote and enhance ferroportin disease screening.

Journal: Journal of hepatology

Published: June 22, 2020

Hepcidin: immunoanalytic characteristics.

Hepcidin: immunoanalytic characteristics.

Journal: Annales de biologie clinique

Published: September 28, 2018

Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis.

Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis.

Journal: European journal of haematology

Published: May 28, 2018

Added value of hepcidin quantification for the diagnosis and follow-up of anemia-related diseases.

Added value of hepcidin quantification for the diagnosis and follow-up of anemia-related diseases.

Journal: Annales de biologie clinique

Published: January 31, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026