Florence Molinari
4PUBLICATIONS
26CO-AUTHORS
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Publications (4)
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|Jul 02, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variants.Claudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga
|Dec 21, 2023
Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability.Elham Khosrowabadi, Cécile Mignon-Ravix, Florence Riccardi
|Apr 04, 2023
NAPB and developmental and epileptic encephalopathy: Description of the electroclinical profile associated with a novel pathogenic variant.Cécile Mignon-Ravix, Florence Riccardi, Géraldine Daquin
|Apr 03, 2020
A knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment.Mathieu Milh, Pierre Roubertoux, Najoua Biba
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Frequent Collaborators
3 joint publications
Laurent Villard
1 joint publications
Mathieu Milh
1 joint publications
Pierre Roubertoux
1 joint publications
Jean-Christophe Roux
1 joint publications
Pierre-Pascal Lenck-Santini
1 joint publications
Lena Kjellén
1 joint publications
Claudia Cuccurullo
1 joint publications
Emanuele Cerulli Irelli
1 joint publications
Antonella Riva
1 joint publications
Gaetan Lesca
