LICCARDO, RAFFAELLA

LICCARDO, RAFFAELLA  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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‘‘Minor’’ mismatch repair genes involvement in geneticpredisposition to Lynch sindrome 1.5 Abstract in rivista 2010 Duraturo, Francesca; Liccardo, Raffaella; A., Cavallo; DE ROSA, Marina; Izzo, Paola
Association of ‘minor’mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer: probability of synergistic effects 1.5 Abstract in rivista 2010 Duraturo, Francesca; Liccardo, Raffaella; A., Cavallo; DE ROSA, Marina; Izzo, Paola
Synergistic Effects of Low-Risk Variant Alleles in Cancer Predisposition 2.1 Contributo in volume (Capitolo o Saggio) 2013 Duraturo, Francesca; Liccardo, Raffaella; Angela, Cavallo; DE ROSA, Marina; Izzo, Paola
Hereditary gastrointestinal polyposis: Diagnosis, genetic test and risk assessment 1.1 Articolo in rivista 2013 DE ROSA, Marina; Duraturo, Francesca; Liccardo, Raffaella; Izzo, Paola
Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion 1.1 Articolo in rivista 2013 Duraturo, Francesca; Angela, Cavallo; Liccardo, Raffaella; Bianca, Cudia; DE ROSA, Marina; Giuseppe, Diana; Izzo, Paola
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability 1.1 Articolo in rivista 2015 Duraturo, Francesca; Liccardo, Raffaella; Cavallo, Angela; DE ROSA, Marina; Rossi, Giovanni Battista; Izzo, Paola
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome. 1.1 Articolo in rivista 2013 Paparo, L; Rossi, Gb; Delrio, P; Rega, D; Duraturo, Francesca; Liccardo, Raffaella; Debellis, M; Izzo, Paola; DE ROSA, Marina
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects. 1.1 Articolo in rivista 2011 Duraturo, Francesca; Liccardo, Raffaella; Cavallo, A; DE ROSA, Marina; Grosso, Michela; Izzo, Paola
Novel Implications in Molecular Diagnosis of Lynch Syndrome 1.1 Articolo in rivista 2017 Liccardo, Raffaella; DE ROSA, Marina; Izzo, Paola; Duraturo, Francesca
Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors 1.1 Articolo in rivista 2016 Duraturo, Francesca; Liccardo, Raffaella; Izzo, Paola
“Minor” mismatch repair genes involvement in genetic predisposition to lynch syndrome. 4.1 Articoli in Atti di convegno 2009 Duraturo, Francesca; Liccardo, Raffaella; DE ROSA, Marina; Izzo, Paola
SALT-INDUCIBLE KINASE 1 MESSENGER ALTERATIONS ARE INVOLVED IN COLORECTAL TUMORIGENESIS 4.3 Poster 2013 DE ROSA, Marina; Duraturo, Francesca; Liccardo, Raffaella; Izzo, Paola
Primary colon cancer cell cultures re-express e-cadherin during mesenchymal to epithelial reverting transition in vitro 4.3 Poster 2014 DE ROSA, Marina; Duraturo, Francesca; Liccardo, Raffaella; Izzo, Paola
Clinical and anamnestic evaluation rôle for the diagnosis and treatment of families affected by Lynch syndrome. Case report and review of the literature 1.1 Articolo in rivista 2014 Cudia, B; Liccardo, Raffaella; Di Carlo, G; Damiano, G; Monte, L; Ignazio, A; Izzo, Paola; Duraturo, Francesca
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 1.5 Abstract in rivista 2015 Costabile, Valeria; Duraturo, Francesca; Liccardo, Raffaella; Nitsch, Lucio; Avallone, Luigi; Izzo, Paola; DE ROSA, Marina
Involvement of large rearrangements in MSH6 and PMS2 genes in southern Italian patients with Lynch syndrome 1.1 Articolo in rivista 2018 Lo Monte, A. I.; Cudia, B.; Liccardo, R.; Izzo, P.; Duraturo, F.
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients. 1.1 Articolo in rivista 2018 Liccardo, R.; DE ROSA, Marina; Rossi, G. B.; Riegler, G.; Izzo, P.; Duraturo, F.
Identification and molecular characterization of a novel mutation in MSH2 gene in a Lynch syndrome family 1.1 Articolo in rivista 2017 Cudia, Bianca; Ignazio Lo Monte, Attilio; Liccardo, Raffaella; Izzo, Paola; Duraturo, Francesca
Incomplete segregation of MSH6 mutations with phenotype of Lynch syndrome. 1.5 Abstract in rivista 2014 Liccardo, Raffaella; DE ROSA, Marina; Battista Rossi, Giovanni; Carlomagno, Nicola; Izzo, Paola; Duraturo, Francesca
Genetics, diagnosis and treatment of lynch syndrome: Old lessons and current challenges (Review) 1.8 Articolo in rassegna (review) 2019 Duraturo, Francesca; Liccardo, Raffaella; DE ROSA, Marina; Izzo, Paola