Cardiovascular Implications in Idiopathic and Syndromic Obesity in Childhood: An Update

by Delvecchio, Maurizio, Pastore, Carmela, Valente, Federica, Giordano, Paola
Published in Front Endocrinol (Lausanne) (2020)

Autoimmune haematological disorders in two Italian children with Kabuki Syndrome

by Giordano, Paola, Lassandro, Giuseppe, Sangerardi, Maria, Faienza, Maria Felicia, Valente, Federica, Martire, Baldassarre
Published 2014

How Physical Activity across the Lifespan Can Reduce the Impact of Bone Ageing: A Literature Review

by Faienza, Maria Felicia, Lassandro, Giuseppe, Chiarito, Mariangela, Valente, Federica, Ciaccia, Loredana, Giordano, Paola
Published in Int J Environ Res Public Health (2020)

Innovative use of recombinant activated factor VII during physical rehabilitation in an Italian child with Glanzmann’s thromboasthenia

by Giordano, Paola, Lassandro, Giuseppe, Tesse, Riccardina, Longo, Stefania, Valente, Federica, Cappiello, Anna Rita, Coppola, Antonio
Published 2013

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes

by Boonen, Susanne Eriksen, Freschi, Andrea, Christensen, Rikke, Valente, Federica Maria, Lildballe, Dorte Launholt, Perone, Lucia, Palumbo, Orazio, Carella, Massimo, Uldbjerg, Niels, Sparago, Angela, Riccio, Andrea, Cerrato, Flavia
Published in Clin Epigenetics (2016)

Endothelial and Metabolic Function Interactions in Overweight/Obese Children: The Role of High-Molecular Weight Adiponectin

by Ciccone, Marco Matteo, Faienza, Maria Felicia, Altomare, Maria, Nacci, Carmela, Montagnani, Monica, Valente, Federica, Cortese, Francesca, Gesualdo, Michele, Zito, Annapaola, Mancarella, Rossana, Leogrande, Domenico, Viola, Domenico, Scicchitano, Pietro, Giordano, Paola
Published in J Atheroscler Thromb (2016)

Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice

by Freschi, Andrea, Hur, Stella K., Valente, Federica Maria, Ideraabdullah, Folami Y., Sparago, Angela, Gentile, Maria Teresa, Oneglia, Andrea, Di Nucci, Diego, Colucci-D’Amato, Luca, Thorvaldsen, Joanne L., Bartolomei, Marisa S., Riccio, Andrea, Cerrato, Flavia
Published in PLoS Genet (2018)

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus

by Valente, Federica Maria, Sparago, Angela, Freschi, Andrea, Hill-Harfe, Katherine, Maas, Saskia M., Frints, Suzanna Gerarda Maria, Alders, Marielle, Pignata, Laura, Franzese, Monica, Angelini, Claudia, Carli, Diana, Mussa, Alessandro, Gazzin, Andrea, Gabbarini, Fulvio, Acurzio, Basilia, Ferrero, Giovanni Battista, Bliek, Jet, Williams, Charles A., Riccio, Andrea, Cerrato, Flavia
Published in Genet Med (2019)