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Annual Review of Pharmacology and Toxicology|September 11, 2024
Treating Sickle Cell Disease: Gene Therapy ApproachesMarina Cavazzana, Alice Corsia, Megane Brusson, et al.
Annual Review of Genomics and Human Genetics|August 25, 2023
Sickle Cell Disease: From Genetics to Curative ApproachesGiulia Hardouin, Elisa Magrin, Alice Corsia, et al.
British Journal of Haematology|February 21, 2025
Maternal and perinatal outcomes of sickle cell disease in pregnancy: A nationwide study in FranceAlice Corsia, Laure Joseph, Nathanael Beeker, et al.
Orphanet Journal of Rare Diseases|March 18, 2017
A survey of resistance to colchicine treatment for French patients with familial Mediterranean feverAlice Corsia, Sophie Georgin-Lavialle, Véronique Hentgen, et al.
BMJ (Clinical Research Ed.)|June 5, 2020
Kawasaki-like multisystem inflammatory syndrome in children during the covid-19 pandemic in Paris, France: prospective observational studyJulie Toubiana, Clément Poirault, Alice Corsia, et al.
The Journal of Pathology|May 17, 2021
SMARCA4-deficient rhabdoid tumours show intermediate molecular features between SMARCB1-deficient rhabdoid tumours and small cell carcinomas of the ovary, hypercalcaemic typeMamy Andrianteranagna, Joanna Cyrta, Julien Masliah-Planchon, et al.
Nature Communications|April 1, 2025
Severe inflammation and lineage skewing are associated with poor engraftment of engineered hematopoietic stem cells in patients with sickle cell diseaseSteicy Sobrino, Laure Joseph, Elisa Magrin, et al.
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