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Peroxisomal acyl-CoA-oxidase deficiency: two new cases.
Carrozzo R, Bellini C, Lucioli S, Deodato F, Cassandrini D, Cassanello M, Caruso U, Rizzo C, Rizza T, Napolitano ML, Wanders RJ, Jakobs C, Bruno C, Santorelli FM, Dionisi-Vici C, Bonioli E. Carrozzo R, et al. Among authors: bonioli e. Am J Med Genet A. 2008 Jul 1;146A(13):1676-81. doi: 10.1002/ajmg.a.32298. Am J Med Genet A. 2008. PMID: 18536048
Sebaceous nevus syndrome: report of two cases.
Bonioli EV, Bertola A, Di Stefano A, Bellini C. Bonioli EV, et al. Pediatr Neurol. 1997 Jul;17(1):77-9. doi: 10.1016/s0887-8994(97)80672-8. Pediatr Neurol. 1997. PMID: 9308983
Congenital pulmonary lymphangiectasia.
Bellini C, Boccardo F, Campisi C, Bonioli E. Bellini C, et al. Among authors: bonioli e. Orphanet J Rare Dis. 2006 Oct 30;1:43. doi: 10.1186/1750-1172-1-43. Orphanet J Rare Dis. 2006. PMID: 17074089 Free PMC article. Review.
A diagnostic flow chart for non-immune hydrops fetalis.
Bellini C, Hennekam RC, Bonioli E. Bellini C, et al. Among authors: bonioli e. Am J Med Genet A. 2009 May;149A(5):852-3. doi: 10.1002/ajmg.a.32677. Am J Med Genet A. 2009. PMID: 19334092 No abstract available.
Fumarate hydratase deficiency.
Bonioli E, Di Stefano A, Peri V, Caruso U, Cerone R, Lamantea E, Taroni F, Bellini C. Bonioli E, et al. J Inherit Metab Dis. 1998 Jun;21(4):435-6. doi: 10.1023/a:1005379330187. J Inherit Metab Dis. 1998. PMID: 9700607 No abstract available.
Partial agenesis of corpus callosum in LEOPARD syndrome.
Bonioli E, Di Stefano A, Costabel S, Bellini C. Bonioli E, et al. Int J Dermatol. 1999 Nov;38(11):855-62. doi: 10.1046/j.1365-4362.1999.00834.x. Int J Dermatol. 1999. PMID: 10583620 No abstract available.
110 results