Browsing by Author "Gener, Blanca"
Now showing items 1-3 of 3
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Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report
Vado Ranedo, Yerai ; Errea Dorronsoro, Javier; Llano-Rivas, Isabel; Gorria, Nerea; Pereda, Arrate; Gener, Blanca; Garcia-Naveda, Laura; Perez de Nanclares, Guiomar (Biomed Central, 2018-12-27)BackgroundSilver-Russell Syndrome (SRS) is a rare growth-related genetic disorder mainly characterized by prenatal and postnatal growth failure. Although molecular causes are not clear in all cases, the most common mechanisms ... -
Reiterative Infusions of MSCs Improve Pediatric Osteogenesis Imperfecta Eliciting a Pro-Osteogenic Paracrine Response: TERCELOI Clinical Trial
Infante, Arantza; Gener, Blanca; Vázquez Ronco, Miguel; Olivares, Nerea; Arrieta, Arantza; Grau, Gema; Llano Rivas, Isabel; Madero, Luis; Bueno, Ana María; Sagastizabal, Belén; Gerovska, Daniela; Araúzo Bravo, Marcos J.; Astigarraga Aguirre, María Iciar; Rodríguez López, Clara Isabel (John Wiley & Sons, 2021-01-13)Background Osteogenesis imperfecta (OI) is a rare genetic disease characterized by bone fragility, with a wide range in the severity of clinical manifestations. The majority of cases are due to mutations in the COL1A1 or ... -
Reiterative infusions of MSCs improve pediatric osteogenesis imperfecta eliciting a pro-osteogenic paracrine response: TERCELOI clinical trial
Infante, Arantza; Gener, Blanca; Vázquez, Miguel; Olivares, Nerea; Arrieta, Arantza; Grau, Gema; Llano, Isabel; Madero, Luis; Bueno, Ana Maria; Sagastizabal, Belén; Gerovska, Daniela; Araúzo Bravo, Marcos J.; Astigarraga Aguirre, María Iciar; Rodríguez López, Clara Isabel (Wiley, 2021-01-12)Background Osteogenesis imperfecta (OI) is a rare genetic disease characterized by bone fragility, with a wide range in the severity of clinical manifestations. The majority of cases are due to mutations in the COL1A1 or ...