Ebstein’s anomaly in a child with osteogenesis imperfecta type I

Por D’Eufemia, Patrizia, Celli, Mauro, Versacci, Paolo, Zambrano, Anna, Lodato, Valentina, Persiani, Pietro, Sangiorgi, Luca
Publicado em 2011

Chiari type I malformation, syncope, headache, hypoglycemia and hepatic steatosis in an 8-year old girl: a causal association?

Por Tarani, Luigi, Del Balzo, Francesca, Costantino, Francesco, Properzi, Enrico, D’Eufemia, Patrizia, Liberati, Natascia, Spalice, Alberto
Publicado em 2010

Osteogenesis imperfecta and clubfoot—a rare combination: Case report and review of the literature

Por Persiani, Pietro, Ranaldi, Filippo Maria, Martini, Lorena, Zambrano, Anna, Celli, Mauro, D’Eufemia, Patrizia, Villani, Ciro
Publicado no Medicine (Baltimore) (2016)

Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case report

Por D’Eufemia, Patrizia, Palombaro, Marta, Lodato, Valentina, Zambrano, Anna, Celli, Mauro, Persiani, Pietro, De Bari, Maria Pia, Sangiorgi, Luca
Publicado em 2012

Isolated olecranon fractures in children affected by osteogenesis imperfecta type I treated with single screw or tension band wiring system: Outcomes and pitfalls in relation to bo...

Por Persiani, Pietro, Ranaldi, Filippo M., Graci, Jole, De Cristo, Claudia, Zambrano, Anna, D’Eufemia, Patrizia, Martini, Lorena, Villani, Ciro
Publicado no Medicine (Baltimore) (2017)

Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

Por Swinnen, Freya KR, Coucke, Paul J, De Paepe, Anne M, Symoens, Sofie, Malfait, Fransiska, Gentile, Filomena V, Sangiorgi, Luca, D'Eufemia, Patrizia, Celli, Mauro, Garretsen, Ton JTM, Cremers, Cor WRJ, Dhooge, Ingeborg JM, De Leenheer, Els MR
Publicado em 2011