Publications by authors named "Mathilde Bonnot Ruget"

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Diagnostic challenge between a frequent polygenic hypocholesterolemia and an unusual Smith Lemli Opitz syndrome related to bi-allelic mutations.
Mathilde Bonnot Ruget, Philippe Moulin, Cécile Pagan, David Cheillan, Oriane Marmontel

Clin Chem Lab Med· August 2024

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Artefactual decrease in the fluorescence intensity of hereditary spherocytosis EMA test related to statins.
Bonnot Ruget Mathilde, Demeule Caroline, Titraoui Fatima, Hassani Kazem, Lagros Oceane

Blood Cells Mol Dis· January 2023

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