Ophélie Evrard
2PUBLICATIONS
10CO-AUTHORS
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Publications (2)
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|Jan 21, 2026
Adult male patients with DKC1 mutations present early-onset pulmonary fibrosis and severe prognosis.Ophélie Evrard, Quentin Philippot, Caroline Kannengiesser
|Aug 08, 2024
Intragenic deletions in SPTB are associated with hereditary spherocytosis: Series of 12 cases.Ophélie Evrard, Alexis Billes, Catherine Badens
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Frequent Collaborators
1 joint publications
Catherine Badens
1 joint publications
Philippe Joly
1 joint publications
Céline Renoux
1 joint publications
Caroline Kannengiesser
1 joint publications
Marie Pierre Debray
1 joint publications
David Montani
1 joint publications
Vincent Cottin
1 joint publications
Héléne Morel
1 joint publications
Bruno Crestani
1 joint publications
Raphaël Borie
