miRNA deregulation and relationship with metabolic parameters after Mediterranean dietary intervention in BRCA-mutated women von De Summa, Simona, Traversa, Debora, Daniele, Antonella, Palumbo, Orazio, Carella, Massimo, Stallone, Raffaella, Tufaro, Antonio, Oliverio, Andreina, Bruno, Eleonora, Digennaro, Maria, Danza, Katia, Pasanisi, Patrizia, Tommasi, Stefania

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Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines via the mTOR/GSK-3β Axis von Etna, Marilena P, Severa, Martina, Licursi, Valerio, Pardini, Manuela, Cruciani, Melania, Rizzo, Fabiana, Giacomini, Elena, Macchia, Gianfranco, Palumbo, Orazio, Stallone, Raffaella, Carella, Massimo, Livingstone, Mark, Negri, Rodolfo, Pellegrini, Sandra, Coccia, Eliana M

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A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report von Palumbo, Orazio, Palumbo, Pietro, Palladino, Teresa, Stallone, Raffaella, Zelante, Leopoldo, Carella, Massimo

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Microdeletion of 12q24.31: Report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms von Palumbo, Orazio, Palumbo, Pietro, Delvecchio, Maurizio, Palladino, Teresa, Stallone, Raffaella, Crisetti, Matteo, Zelante, Leopoldo, Carella, Massimo

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Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome von Palumbo, Pietro, Accadia, Maria, Leone, Maria P., Palladino, Teresa, Stallone, Raffaella, Carella, Massimo, Palumbo, Orazio

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3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination von Palumbo, Orazio, D'Agruma, Leonardo, Minenna, Adelaide Franca, Palumbo, Pietro, Stallone, Raffaella, Palladino, Teresa, Zelante, Leopoldo, Carella, Massimo

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Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus von De Bonis, Patrizia, Laborante, Antonio, Pizzicoli, Costantina, Stallone, Raffaella, Barbano, Raffaela, Longo, Costanza, Mazzilli, Emilio, Zelante, Leopoldo, Bisceglia, Luigi

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Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders von Palumbo, Orazio, Accadia, Maria, Palumbo, Pietro, Leone, Maria Pia, Scorrano, Antonio, Palladino, Teresa, Stallone, Raffaella, Bonaglia, Maria Clara, Carella, Massimo

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Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancer von Mazza, Tommaso, Mazzoccoli, Gianluigi, Fusilli, Caterina, Capocefalo, Daniele, Panza, Anna, Biagini, Tommaso, Castellana, Stefano, Gentile, Annamaria, De Cata, Angelo, Palumbo, Orazio, Stallone, Raffaella, Rubino, Rosa, Carella, Massimo, Piepoli, Ada

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Abstract 5394: Initial results from TRANSCAN ERA-NET BREMIR project: MicroRNAs expression profiling for identification of breast cancer patients at high risk to develop distant met... von Parrella, Paola, Barbano, Raffaela, Evron, Ella, Pasculli, Barbara, Palumbo, Orazio, Rendina, Michelina, Stallone, Raffaella, Coco, Michela, Fontana, Andrea, Mazza, Tommaso, Copetti, Massimiliano, Valori, Vanna Maria, Morritti, Maria, Graziano, Paolo, Murgo, Roberto, Maiello, Evaristo, Carella, Massimo, Fazio, Vito Michele, Esteller, Manel

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Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay von Palumbo, Pietro, Palumbo, Orazio, Leone, Maria Pia, Stallone, Raffaella, Palladino, Teresa, Zelante, Leopoldo, Carella, Massimo

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8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: Case report and critical review of the literature von Palumbo, Orazio, Palumbo, Pietro, Stallone, Raffaella, Palladino, Teresa, Zelante, Leopoldo, Carella, Massimo

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Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing von Leone, Maria Pia, Palumbo, Pietro, Ortore, Rocco, Castellana, Stefano, Palumbo, Orazio, Melchionda, Salvatore, Palladino, Teresa, Stallone, Raffaella, Mazza, Tommaso, Cocchi, Roberto, Carella, Massimo

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Clinical and molecular characterization of a de novo 19p13.3 microdeletion von Palumbo, Pietro, Palumbo, Orazio, Leone, Maria Pia, Stallone, Raffaella, Palladino, Teresa, Zelante, Leopoldo, Carella, Massimo

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An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review von Palumbo, Orazio, Palumbo, Pietro, Palladino, Teresa, Stallone, Raffaella, Miroballo, Mattia, Piemontese, Maria Rosaria, Zelante, Leopoldo, Carella, Massimo

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Interstitial 16p13.3 microduplication: Case report and critical review of genotype–phenotype correlation von Mattina, Teresa, Palumbo, Orazio, Stallone, Raffaella, Pulvirenti, Rita Maria, Di Dio, Laura, Pavone, Piero, Carella, Massimo, Pavone, Lorenzo

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PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature von Palumbo, Orazio, Palumbo, Pietro, Leone, Maria P., Stallone, Raffaella, Palladino, Teresa, Vendemiale, Marcella, Palladino, Stefano, Papadia, Francesco, Carella, Massimo, Fischetto, Rira

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Clinical and molecular characterization of a de novo 19p13.3 microdeletion von Palumbo, Pietro, Palumbo, Orazio, Leone, Maria Pia, Stallone, Raffaella, Palladino, Teresa, Zelante, Leopoldo, Carella, Massimo

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Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay von Palumbo, Pietro, Palumbo, Orazio, Leone, Maria Pia, Stallone, Raffaella, Palladino, Teresa, Zelante, Leopoldo, Carella, Massimo

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An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review von Palumbo, Orazio, Palumbo, Pietro, Palladino, Teresa, Stallone, Raffaella, Miroballo, Mattia, Piemontese, Maria Rosaria, Zelante, Leopoldo, Carella, Massimo

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