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The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|November 29, 2021
Impulsivity and eating disorders: The relationship between serum 25-hydroxyvitamin D and different impulsivity facets in a transdiagnostic samplePaolo Meneguzzo, Cecilia Mancini, Aurora Ormitti, et al.
Neurobiology of Disease|April 18, 2015
Blood metal levels and related antioxidant enzyme activities in patients with ataxia telangiectasiaStefania Squadrone, Paola Brizio, Cecilia Mancini, et al.
Neuroendocrinology|August 23, 2005
Thyroid hormones affect neurogenesis in the dentate gyrus of adult ratPatrizia Ambrogini, Riccardo Cuppini, Paola Ferri, et al.
Eating and Weight Disorders : EWD|December 14, 2020
Health-related quality of life assessment in eating disorders: adjustment and validation of a specific scale with the inclusion of an interpersonal domainPaolo Meneguzzo, Patrizia Todisco, Sofia Calonaci, et al.
Haematologica|June 13, 2012
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assayPaola Quarello, Emanuela Garelli, Alfredo Brusco, et al.
Genes|May 28, 2022
Complex Presentation of Hao-Fountain Syndrome Solved by Exome Sequencing Highlighting Co-Occurring Genomic VariantsManuela Priolo, Cecilia Mancini, Simone Pizzi, et al.
European Journal of Medical Genetics|November 17, 2018
A fetal case of microphthalmia and limb anomalies with abnormal neuronal migration associated with SMOC1 biallelic variantsCecilia Mancini, Andrea Zonta, Giovanni Botta, et al.
Neurogenetics|May 4, 2012
Megalencephalic leukoencephalopathy with subcortical cysts type 1 (MLC1) due to a homozygous deep intronic splicing mutation (c.895-226T>G) abrogated in vitro using an antisense morpholino oligonucleotideCecilia Mancini, Giovanna Vaula, Laura Scalzitti, et al.
Frontiers in Neurology|February 24, 2023
Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephalyEmanuela Salzano, Marcello Niceta, Simone Pizzi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2023
Natural history of MRAS-related Noonan syndrome: Evidence of mild adult-onset left ventricular hypertrophy and neuropsychiatric featuresManuela Priolo, Cecilia Mancini, Francesca Clementina Radio, et al.
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