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Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|May 19, 2025
Improved diagnosis of glioblastoma, IDH-wildtype, metastasis through molecular and DNA methylation profiling: Two case reportsAlexandre Bertucci, Elise Kaspi, Marylin Barrie, et al.
Diagnostics (Basel, Switzerland)|March 14, 2026
Ciliary Beat Frequency and Pattern: An Accessible Tool for the Screening of Primary Ciliary DyskinesiaElise Kaspi, Julie Mazenq, Adrien Pagin, et al.
BMC Genetics|October 19, 2007
Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areasBarbara Royer, Dinesh C Soares, Paul N Barlow, et al.
Clinical Chemistry and Laboratory Medicine|January 8, 2018
Detection of EGFR, KRAS and BRAF mutations in metastatic cells from cerebrospinal fluidDiane Frankel, Isabelle Nanni-Metellus, Andrée Robaglia-Schlupp, et al.
Human Molecular Genetics|August 23, 2008
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPARBarbara Royer-Zemmour, Magali Ponsole-Lenfant, Hyam Gara, et al.
Oncotarget|December 23, 2015
Detection of EpCAM-positive microparticles in pleural fluid: A new approach to mini-invasively identify patients with malignant pleural effusionsElisa Roca, Romaric Lacroix, Coralie Judicone, et al.
Cells|April 28, 2016
A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated CardiomyopathyDamien Galant, Bénédicte Gaborit, Camille Desgrouas, et al.
Scientific Reports|July 18, 2019
Extracellular vesicles from T cells overexpress miR-146b-5p in HIV-1 infection and repress endothelial activationEstelle Balducci, Aurélie S Leroyer, Romaric Lacroix, et al.
Human Molecular Genetics|July 5, 2011
High prevalence of laminopathies among patients with metabolic syndromeAnne Dutour, Patrice Roll, Bénédicte Gaborit, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndromeJacques Rochette, Patrice Roll, Ying-Hui Fu, et al.
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