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Osteogenesis imperfecta.
Ben Amor M, Rauch F, Monti E, Antoniazzi F. Ben Amor M, et al. Among authors: monti e. Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2:397-405. Pediatr Endocrinol Rev. 2013. PMID: 23858623 Review.
GH in combination with bisphosphonate treatment in osteogenesis imperfecta.
Antoniazzi F, Monti E, Venturi G, Franceschi R, Doro F, Gatti D, Zamboni G, Tatò L. Antoniazzi F, et al. Among authors: monti e. Eur J Endocrinol. 2010 Sep;163(3):479-87. doi: 10.1530/EJE-10-0208. Epub 2010 Jun 30. Eur J Endocrinol. 2010. PMID: 20592128 Clinical Trial.
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen.
Venturi G, Gandini A, Monti E, Dalle Carbonare L, Corradi M, Vincenzi M, Valenti MT, Valli M, Pelilli E, Boner A, Mottes M, Antoniazzi F. Venturi G, et al. Among authors: monti e. J Bone Miner Res. 2012 Mar;27(3):723-8. doi: 10.1002/jbmr.1480. J Bone Miner Res. 2012. PMID: 22113968 Free article.
The SHOX gene and the short stature. Roundtable on diagnosis and treatment of short stature due to SHOX haploinsufficiency: how genetics, radiology and anthropometry can help the pediatrician in the diagnostic process Padova (April 20th, 2011).
De Sanctis V, Tosetto I, Iughetti L, Antoniazzi F, Clementi M, Toffolutti T, Facchin P, Monti E, Pisanello L, Tonini G, Greggio NA. De Sanctis V, et al. Among authors: monti e. Pediatr Endocrinol Rev. 2012 Aug;9(4):727-33. Pediatr Endocrinol Rev. 2012. PMID: 23304810
382 results