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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: lala r. 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.
Genetics of McCune-Albright syndrome.
de Sanctis L, Delmastro L, Russo MC, Matarazzo P, Lala R, de Sanctis C. de Sanctis L, et al. Among authors: lala r. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:577-82. doi: 10.1515/jpem.2006.19.s2.577. J Pediatr Endocrinol Metab. 2006. PMID: 16789620 Review.
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: lala r. 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
McCune-Albright syndrome: a longitudinal clinical study of 32 patients.
de Sanctis C, Lala R, Matarazzo P, Balsamo A, Bergamaschi R, Cappa M, Cisternino M, de Sanctis V, Lucci M, Franzese A, Ghizzoni L, Pasquino AM, Segni M, Rigon F, Saggese G, Bertelloni S, Buzi F. de Sanctis C, et al. Among authors: lala r. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):817-26. doi: 10.1515/jpem.1999.12.6.817. J Pediatr Endocrinol Metab. 1999. PMID: 10614538 Review.
123 results