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Scientific Reports|May 8, 2015
A versatile clearing agent for multi-modal brain imagingIrene Costantini, Jean-Pierre Ghobril, Antonino Paolo Di Giovanna, et al.
Human Molecular Genetics|October 13, 2025
Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortexAntonio Falace, Léa Corbières, Lucas Silvagnoli, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissuesDanila Di Meo, Michele Sorelli, Josephine Ramazzotti, et al.
Human Molecular Genetics|August 15, 2019
Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsyCristiana Pelorosso, Françoise Watrin, Valerio Conti, et al.
Communications Biology|November 5, 2025
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissuesDanila Di Meo, Michele Sorelli, Josephine Ramazzotti, et al.
Journal of Personalized Medicine|April 23, 2022
Prospective Evaluation of Ghrelin and Des-Acyl Ghrelin Plasma Levels in Children with Newly Diagnosed Epilepsy: Evidence for Reduced Ghrelin-to-Des-Acyl Ghrelin Ratio in Generalized EpilepsiesAnna-Maria Costa, Tommaso Lo Barco, Elisabetta Spezia, et al.
Breast Cancer Research : BCR|March 25, 2021
Circulating tumor cells and palbociclib treatment in patients with ER-positive, HER2-negative advanced breast cancer: results from a translational sub-study of the TREnd trialFrancesca Galardi, Francesca De Luca, Chiara Biagioni, et al.
Epilepsia|May 11, 2019
Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasiaKatja Kobow, Mark Ziemann, Harikrishnan Kaipananickal, et al.
Seizure|February 23, 2021
Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetaseAnna Maria Buccoliero, Chiara Caporalini, Mirko Scagnet, et al.
Journal of Visualized Experiments : Jove|December 30, 2017
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain MalformationsValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
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