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Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society.
Ippolito E, Bray EW, Corsi A, De Maio F, Exner UG, Robey PG, Grill F, Lala R, Massobrio M, Pinggera O, Riminucci M, Snela S, Zambakidis C, Bianco P; European Pediatric Orthopaedic Society. Ippolito E, et al. Among authors: bianco p. J Pediatr Orthop B. 2003 May;12(3):155-77. doi: 10.1097/01.bpb.0000064021.41829.94. J Pediatr Orthop B. 2003. PMID: 12703030
Fibrous dysplasia as a stem cell disease.
Riminucci M, Saggio I, Robey PG, Bianco P. Riminucci M, et al. Among authors: bianco p. J Bone Miner Res. 2006 Dec;21 Suppl 2:P125-31. doi: 10.1359/jbmr.06s224. J Bone Miner Res. 2006. PMID: 17229001 Free article. Review.
Notochordal inclusions in the vertebral bone marrow.
Corsi A, De Maio F, Mancini F, Ippolito E, Riminucci M, Bianco P. Corsi A, et al. Among authors: bianco p. J Bone Miner Res. 2008 Apr;23(4):572-5. doi: 10.1359/jbmr.071204. J Bone Miner Res. 2008. PMID: 18072879 Free article.
Osteoblast-specific expression of the fibrous dysplasia (FD)-causing mutation Gsα(R201C) produces a high bone mass phenotype but does not reproduce FD in the mouse.
Remoli C, Michienzi S, Sacchetti B, Consiglio AD, Cersosimo S, Spica E, Robey PG, Holmbeck K, Cumano A, Boyde A, Davis G, Saggio I, Riminucci M, Bianco P. Remoli C, et al. Among authors: bianco p. J Bone Miner Res. 2015 Jun;30(6):1030-43. doi: 10.1002/jbmr.2425. J Bone Miner Res. 2015. PMID: 25487351 Free PMC article.
A novel GNAS1 mutation, R201G, in McCune-albright syndrome.
Riminucci M, Fisher LW, Majolagbe A, Corsi A, Lala R, De Sanctis C, Robey PG, Bianco P. Riminucci M, et al. Among authors: bianco p. J Bone Miner Res. 1999 Nov;14(11):1987-9. doi: 10.1359/jbmr.1999.14.11.1987. J Bone Miner Res. 1999. PMID: 10571700 Free article. No abstract available.
683 results