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Journal of Translational Autoimmunity|November 18, 2024
C3 glomerulopathy is highly prevalent in French PolynesiaNelly Candela, Nicolas Benichou, Mathilde Lefebvre, et al.
Pediatric Radiology|January 12, 2019
Prenatal ultrasonography of autosomal dominant polycystic kidney disease mimicking recessive type: case seriesJuliette Garel, Mathilde Lefebvre, Marie Cassart, et al.
Fetal and Pediatric Pathology|January 15, 2019
TRAP Sequence in Monochorionic/Monoamniotic (MC/MA) Discordant Twins: Two Cases Treated with Fetoscopic Laser SurgeryGabriele Tonni, Gianpaolo Grisolia, Paolo Zampriolo, et al.
Biomolecules|January 8, 2025
In-Depth Phenotyping of <i>PIGW</i>-Related Disease and Its Role in 17q12 Genomic DisorderAgnese Feresin, Mathilde Lefebvre, Emilie Sjøstrøm, et al.
FEBS Letters|March 20, 2014
A comprehensive approach to determining BER capacities and their change with aging in Drosophila melanogaster mitochondria by oligonucleotide microarrayIsabelle Garreau-Balandier, Mathilde Lefebvre, Sophie Jacquard, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|November 3, 2021
CCR5 Blockade in Inflammatory PML and PML-IRIS Associated With Chronic Inflammatory Diseases' TreatmentsRaphael Bernard-Valnet, Xavier Moisset, Nicolas Maubeuge, et al.
Iscience|January 6, 2026
STAG2-truncating variants reveal a mosaic STAG2 inactivation pattern and compensatory mechanisms involving cohesin complex remodelingMacarena Moronta Gines, Marja W Wessels, Valentina Casa, et al.
Brain Structure & Function|November 15, 2022
In mice and humans, brain microvascular contractility matures postnatallyLeila Slaoui, Alice Gilbert, Armelle Rancillac, et al.
Pediatric Neurology|April 16, 2025
Glycosylphosphatidylinositol Biosynthesis Defect Due To Novel Biallelic Pathogenic Variants in PIGWNazim Rabouhi, Smrithi Salian, Hind Benkerroum, et al.
Prenatal Diagnosis|November 19, 2016
Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 casesAude Tessier, Mélie Sarreau, Fanny Pelluard, et al.
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