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Correction to: Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database.
Marini F, Giusti F, Fossi C, Cioppi F, Cianferotti L, Masi L, Boaretto F, Zovato S, Cetani F, Colao A, Davì MV, Faggiano A, Fanciulli G, Ferolla P, Ferone D, Loli P, Mantero F, Marcocci C, Opocher G, Beck-Peccoz P, Persani L, Scillitani A, Guizzardi F, Spada A, Tomassetti P, Tonelli F, Brandi ML. Marini F, et al. Among authors: masi l. Endocrine. 2018 Oct;62(1):234-241. doi: 10.1007/s12020-018-1668-3. Endocrine. 2018. PMID: 30032405
Microencapsulation of human parathyroid cells: an "in vitro" study.
Picariello L, Benvenuti S, Recenti R, Formigli L, Falchetti A, Morelli A, Masi L, Tonelli F, Cicchi P, Brandi ML. Picariello L, et al. Among authors: masi l. J Surg Res. 2001 Mar;96(1):81-9. doi: 10.1006/jsre.2000.6054. J Surg Res. 2001. PMID: 11181000
Two novel mutations at exon 8 of the Sequestosome 1 (SQSTM1) gene in an Italian series of patients affected by Paget's disease of bone (PDB).
Falchetti A, Di Stefano M, Marini F, Del Monte F, Mavilia C, Strigoli D, De Feo ML, Isaia G, Masi L, Amedei A, Cioppi F, Ghinoi V, Bongi SM, Di Fede G, Sferrazza C, Rini GB, Melchiorre D, Matucci-Cerinic M, Brandi ML. Falchetti A, et al. Among authors: masi l. J Bone Miner Res. 2004 Jun;19(6):1013-7. doi: 10.1359/JBMR.040203. Epub 2004 Feb 2. J Bone Miner Res. 2004. PMID: 15125799 Free article.
288 results