The G53D Mutation in Kir6.2 (KCNJ11) Is Associated with Neonatal Diabetes and Motor Dysfunction in Adulthood that Is Improved with Sulfonylurea Therapy

Por Koster, Joseph C., Cadario, Francesco, Peruzzi, Cinzia, Colombo, Carlo, Nichols, Colin G., Barbetti, Fabrizio
Publicado em 2008

Vitamin D status in cord blood and newborns: ethnic differences

Por Cadario, Francesco, Savastio, Silvia, Pozzi, Erica, Capelli, Antonella, Dondi, Elena, Gatto, Miriam, Zaffaroni, Mauro, Bona, Gianni
Publicado em 2013

Vitamin D Deficiency and Glycemic Status in Children and Adolescents with Type 1 Diabetes Mellitus

Por Savastio, Silvia, Cadario, Francesco, Genoni, Giulia, Bellomo, Giorgio, Bagnati, Marco, Secco, Gioel, Picchi, Raffaella, Giglione, Enza, Bona, Gianni
Publicado no PLoS One (2016)

High Prevalence of Vitamin D Deficiency in Native versus Migrant Mothers and Newborns in the North of Italy: A Call to Act with a Stronger Prevention Program

Por Cadario, Francesco, Savastio, Silvia, Magnani, Corrado, Cena, Tiziana, Pagliardini, Veronica, Bellomo, Giorgio, Bagnati, Marco, Vidali, Matteo, Pozzi, Erica, Pamparana, Stella, Zaffaroni, Mauro, Genoni, Giulia, Bona, Gianni
Publicado no PLoS One (2015)

Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus

Por Colombo, Carlo, Porzio, Ottavia, Liu, Ming, Massa, Ornella, Vasta, Mario, Salardi, Silvana, Beccaria, Luciano, Monciotti, Carla, Toni, Sonia, Pedersen, Oluf, Hansen, Torben, Federici, Luca, Pesavento, Roberta, Cadario, Francesco, Federici, Giorgio, Ghirri, Paolo, Arvan, Peter, Iafusco, Dario, Barbetti, Fabrizio
Publicado em 2008