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Neonatal persistent pulmonary hypertension related to a novel TBX4 mutation: case report and review of the literature.
Maddaloni C, Ronci S, De Rose DU, Bersani I, Campi F, Di Nardo M, Stoppa F, Adorisio R, Amodeo A, Toscano A, Digilio MC, Novelli A, Chello G, Braguglia A, Dotta A, Calzolari F. Maddaloni C, et al. Among authors: toscano a. Ital J Pediatr. 2024 Mar 5;50(1):41. doi: 10.1186/s13052-024-01575-3. Ital J Pediatr. 2024. PMID: 38443964 Free PMC article. Review.
Noonan syndrome and aortic coarctation.
Digilio MC, Marino B, Picchio F, Prandstraller D, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: toscano a. Am J Med Genet. 1998 Nov 2;80(2):160-2. Am J Med Genet. 1998. PMID: 9805134
Deletion 22q11 in patients with interrupted aortic arch.
Marino B, Digilio MC, Persiani M, Di Donato R, Toscano A, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: toscano a. Am J Cardiol. 1999 Aug 1;84(3):360-1, A9. doi: 10.1016/s0002-9149(99)00297-0. Am J Cardiol. 1999. PMID: 10496456
Anatomic patterns of conotruncal defects associated with deletion 22q11.
Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B. Marino B, et al. Among authors: toscano a. Genet Med. 2001 Jan-Feb;3(1):45-8. doi: 10.1097/00125817-200101000-00010. Genet Med. 2001. PMID: 11339377 Free article.
Congenital heart defects in Kabuki syndrome.
Digilio MC, Marino B, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: toscano a. Am J Med Genet. 2001 May 15;100(4):269-74. doi: 10.1002/ajmg.1265. Am J Med Genet. 2001. PMID: 11343317 Review.
699 results