Susanna Pietropaolo

2008-2011 CNRS, Paris, Île-de-France, France 
"Susanna Pietropaolo"
Mean distance: 18.21 (cluster 32)


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Wim E. Crusio post-doc 2008-2011 CNRS


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Wim E. Crusio collaborator 2012- CNRS
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Carreno-Munoz MI, Martins F, Medrano MC, et al. (2017) Potential Involvement of Impaired BKCa Channel Function in Sensory Defensiveness and Some Behavioral Disturbances Induced by Unfamiliar Environment in a Mouse Model of FXS. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
Gauducheau M, Lemaire-Mayo V, D'Amato FR, et al. (2017) Age-specific autistic-like behaviors in heterozygous Fmr1-KO female mice. Autism Research : Official Journal of the International Society For Autism Research
Pietropaolo S, Crusio WE, Feldon J. (2017) Gene-Environment Interactions in Neurodevelopmental Disorders. Neural Plasticity. 2017: 9272804
Lemaire-Mayo V, Subashi E, Henkous N, et al. (2016) Behavioral effects of chronic stress in the Fmr1 mouse model for fragile X syndrome. Behavioural Brain Research. 320: 128-135
Pietropaolo S, Crusio WE, D'amato FR. (2016) Treatment Approaches in Rodent Models for Autism Spectrum Disorder. Current Topics in Behavioral Neurosciences
Oddi D, Subashi E, Middei S, et al. (2015) Early social enrichment rescues adult behavioral and brain abnormalities in a mouse model of fragile X syndrome. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 40: 1113-22
Pietropaolo S, Bellocchio L, Ruiz-Calvo A, et al. (2015) Chronic cannabinoid receptor stimulation selectively prevents motor impairments in a mouse model of Huntington's disease. Neuropharmacology. 89: 368-74
Zhang Y, Bonnan A, Bony G, et al. (2014) Dendritic channelopathies contribute to neocortical and sensory hyperexcitability in Fmr1(-/y) mice. Nature Neuroscience. 17: 1701-9
Pietropaolo S, Goubran MG, Joffre C, et al. (2014) Dietary supplementation of omega-3 fatty acids rescues fragile X phenotypes in Fmr1-Ko mice. Psychoneuroendocrinology. 49: 119-29
Hébert B, Pietropaolo S, Même S, et al. (2014) Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule. Orphanet Journal of Rare Diseases. 9: 124
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