Leoncini, Silvia
Azienda Ospedaliera Universitaria Senese
8 papers on CoChatORCID 0000-0002-7027-1207
Most cited papers
- Verified
New evidences on the altered gut microbiota in autism spectrum disorders
Strati, F., Cavalieri, D., Albanese, D., De Felice, C., Donati, C., Hayek, J., Jousson, O., Leoncini, S., Renzi, D., Calabrò, A., et al. (2017) · Microbiome
Gut microbiota and healthAutism Spectrum Disorder Research
Cited by 1,040
- Verified
Systemic oxidative stress in classic Rett syndrome
De Felice, C., Ciccoli, L., Leoncini, S., Signorini, C., Rossi, M., Vannuccini, L., Guazzi, G., Latini, G., Comporti, M., Valacchi, G., et al. (2009) · Free Radical Biology and Medicine
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 148
- Verified
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome
De Felice, C., Della Ragione, F., Signorini, C., Leoncini, S., Pecorelli, A., Ciccoli, L., Scalabrì, F., Marracino, F., Madonna, M., Belmonte, G., et al. (2014) · Neurobiology of Disease
Genetics and Neurodevelopmental DisordersRedox biology and oxidative stress
Cited by 126
- Verified
Cytokine Dysregulation in MECP2- and CDKL5-Related Rett Syndrome: Relationships with Aberrant Redox Homeostasis, Inflammation, and ω-3 PUFAs
Leoncini, S., De Felice, C., Signorini, C., Zollo, G., Cortelazzo, A., Durand, T., Galano, J.-M., Guerranti, R., Rossi, M., Ciccoli, L., et al. (2015) · Oxidative Medicine and Cellular Longevity
Genetics and Neurodevelopmental DisordersImmunodeficiency and Autoimmune Disorders
Cited by 71
- Verified
Scavenger receptor B1 post-translational modifications in Rett syndrome
Sticozzi, C., Belmonte, G., Pecorelli, A., Cervellati, F., Leoncini, S., Signorini, C., Ciccoli, L., De Felice, C., Hayek, J., & Valacchi, G. (2013) · FEBS Letters
Genetics and Neurodevelopmental DisordersCholesterol and Lipid Metabolism
Cited by 70
- Verified
Oxidative stress in Rett syndrome: natural history, genotype, and variants
Leoncini, S., De Felice, C., Signorini, C., Pecorelli, A., Durand, T., Valacchi, G., Ciccoli, L., & Hayek, J. (2011) · Redox Report
Genetics and Neurodevelopmental DisordersChild Nutrition and Feeding Issues
Cited by 69
- Verified
Redox imbalance and morphological changes in skin fibroblasts in typical Rett syndrome
Signorini, C., Leoncini, S., De Felice, C., Pecorelli, A., Meloni, I., Ariani, F., Mari, F., Amabile, S., Paccagnini, E., Gentile, M., et al. (2014) · Oxidative Medicine and Cellular Longevity
Genetics and Neurodevelopmental DisordersRedox biology and oxidative stress
Cited by 61
- Verified
Alteration of serum lipid profile, SRB1 loss, and impaired Nrf2 activation in CDKL5 disorder
Pecorelli, A., Belmonte, G., Meloni, I., Cervellati, F., Gardi, C., Sticozzi, C., De Felice, C., Signorini, C., Cortelazzo, A., Leoncini, S., et al. (2015) · Free Radical Biology and Medicine
Genetics and Neurodevelopmental DisordersCholesterol and Lipid Metabolism
Cited by 23
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