Catherine Matheron

Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene

Sophie Gandrille, Delphine Borgel, V Eschwege-Gufflet et al. · Blood · 1995 · 91 citations

The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency

Jérôme Duchemin, Sophie Gandrille, Delphine Borgel et al. · Blood · 1995 · 67 citations · Full text

Prehospital Lyophilized Plasma Transfusion for Trauma-Induced Coagulopathy in Patients at Risk for Hemorrhagic Shock

Daniel Jost, Sabine Lemoine, F. Lemoine et al. · JAMA Network Open · 2022 · 66 citations · Full text

Molecular basis for protein S hereditary deficiency: Genetic defects observed in 118 patients with type I and type IIa deficiencies1

Delphine Borgel, Jérôme Duchemin, Martine Alhenc‐Gelas et al. · Journal of Laboratory and Clinical Medicine · 1996 · 60 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +11

An improved electronic microarray-based diagnostic assay for identification ofMEFV mutations

St�phane Moutereau, R. Narwa, Catherine Matheron et al. · Human Mutation · 2004 · 24 citations