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

af Delvecchio, Maurizio, Pastore, Carmela, Valente, Federica, Giordano, Paola
Udgivet i Front Endocrinol (Lausanne) (2020)

Autoimmune haematological disorders in two Italian children with Kabuki Syndrome

af Giordano, Paola, Lassandro, Giuseppe, Sangerardi, Maria, Faienza, Maria Felicia, Valente, Federica, Martire, Baldassarre
Udgivet 2014

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

af Faienza, Maria Felicia, Lassandro, Giuseppe, Chiarito, Mariangela, Valente, Federica, Ciaccia, Loredana, Giordano, Paola
Udgivet i 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

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

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

af 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
Udgivet i Clin Epigenetics (2016)

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

af 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
Udgivet i J Atheroscler Thromb (2016)

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

af 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
Udgivet i PLoS Genet (2018)

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

af 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
Udgivet i Genet Med (2019)