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Expanding the phenotype of 22q11 deletion syndrome: the MURCS association.
Uliana V, Giordano N, Caselli R, Papa FT, Ariani F, Marcocci C, Gianetti E, Martini G, Papakostas P, Rollo F, Meloni I, Mari F, Priolo M, Renieri A, Nuti R. Uliana V, et al. Among authors: martini g. Clin Dysmorphol. 2008 Jan;17(1):13-17. doi: 10.1097/MCD.0b013e3282ef97ee. Clin Dysmorphol. 2008. PMID: 18049074
Paget's disease of bone in Italy.
Gennari L, Merlotti D, Martini G, Nuti R. Gennari L, et al. Among authors: martini g. J Bone Miner Res. 2006 Dec;21 Suppl 2:P14-21. doi: 10.1359/jbmr.06s203. J Bone Miner Res. 2006. PMID: 17229002 Free article.
Secondary osteoporosis.
Gennari C, Martini G, Nuti R. Gennari C, et al. Among authors: martini g. Aging (Milano). 1998 Jun;10(3):214-24. doi: 10.1007/BF03339655. Aging (Milano). 1998. PMID: 9801731 Review.
Current options for the treatment of Paget's disease of the bone.
Merlotti D, Gennari L, Martini G, Nuti R. Merlotti D, et al. Among authors: martini g. Open Access Rheumatol. 2009 Jul 17;1:107-120. doi: 10.2147/oarrr.s4504. eCollection 2009. Open Access Rheumatol. 2009. PMID: 27789985 Free PMC article. Review.
888 results