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Page 1
Clinical, genetic, and cellular analysis of 49 osteopetrotic patients: implications for diagnosis and treatment.
Del Fattore A, Peruzzi B, Rucci N, Recchia I, Cappariello A, Longo M, Fortunati D, Ballanti P, Iacobini M, Luciani M, Devito R, Pinto R, Caniglia M, Lanino E, Messina C, Cesaro S, Letizia C, Bianchini G, Fryssira H, Grabowski P, Shaw N, Bishop N, Hughes D, Kapur RP, Datta HK, Taranta A, Fornari R, Migliaccio S, Teti A. Del Fattore A, et al. Among authors: luciani m. J Med Genet. 2006 Apr;43(4):315-25. doi: 10.1136/jmg.2005.036673. Epub 2005 Aug 23. J Med Genet. 2006. PMID: 16118345 Free PMC article.
Genotype-phenotype relationship in human ATP6i-dependent autosomal recessive osteopetrosis.
Taranta A, Migliaccio S, Recchia I, Caniglia M, Luciani M, De Rossi G, Dionisi-Vici C, Pinto RM, Francalanci P, Boldrini R, Lanino E, Dini G, Morreale G, Ralston SH, Villa A, Vezzoni P, Del Principe D, Cassiani F, Palumbo G, Teti A. Taranta A, et al. Among authors: luciani m. Am J Pathol. 2003 Jan;162(1):57-68. doi: 10.1016/S0002-9440(10)63798-4. Am J Pathol. 2003. PMID: 12507890 Free PMC article.
Association of intermediate osteopetrosis with poikiloderma.
Migliaccio S, Luciani M, Taranta A, De Rossi G, Minisola S, El Hachem M, Bosman C, De Felice L, Boldrini R, Corsi A, Bianco P, Teti A. Migliaccio S, et al. Among authors: luciani m. J Bone Miner Res. 1999 May;14(5):834-6. doi: 10.1359/jbmr.1999.14.5.834. J Bone Miner Res. 1999. PMID: 10320533 Free article. No abstract available.
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations.
Colombo EA, Bazan JF, Negri G, Gervasini C, Elcioglu NH, Yucelten D, Altunay I, Cetincelik U, Teti A, Del Fattore A, Luciani M, Sullivan SK, Yan AC, Volpi L, Larizza L. Colombo EA, et al. Among authors: luciani m. Orphanet J Rare Dis. 2012 Jan 23;7:7. doi: 10.1186/1750-1172-7-7. Orphanet J Rare Dis. 2012. PMID: 22269211 Free PMC article.
Infant leukaemia: clinical, biological and therapeutic advances.
Luciani M, Rana I, Pansini V, Caniglia M, Coletti V, Maraschini A, Lombardi A, De Rossi G. Luciani M, et al. Acta Paediatr Suppl. 2006 Jul;95(452):47-51. doi: 10.1080/08035320600649580. Acta Paediatr Suppl. 2006. PMID: 16801167
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?
Quarello P, Garelli E, Carando A, Cillario R, Brusco A, Giorgio E, Ferrante D, Corti P, Zecca M, Luciani M, Pierri F, Putti MC, Cantarini ME, Farruggia P, Barone A, Cesaro S, Russo G, Fagioli F, Dianzani I, Ramenghi U; AIEOP working group on Diamond Blackfan Anaemia. Quarello P, et al. Among authors: luciani m. Br J Haematol. 2020 Jul;190(1):93-104. doi: 10.1111/bjh.16508. Epub 2020 Feb 21. Br J Haematol. 2020. PMID: 32080838 Free article.
Clofarabine, cyclophosphamide and etoposide for the treatment of relapsed or resistant acute leukemia in pediatric patients.
Miano M, Pistorio A, Putti MC, Dufour C, Messina C, Barisone E, Ziino O, Parasole R, Luciani M, Lo Nigro L, De Rossi G, Varotto S, Bertorello N, Petruzziello F, Calvillo M, Micalizzi C. Miano M, et al. Among authors: luciani m. Leuk Lymphoma. 2012 Sep;53(9):1693-8. doi: 10.3109/10428194.2012.663915. Epub 2012 Mar 13. Leuk Lymphoma. 2012. PMID: 22303898 Clinical Trial.
Recommendations for the use of long-term central venous catheter (CVC) in children with hemato-oncological disorders: management of CVC-related occlusion and CVC-related thrombosis. On behalf of the coagulation defects working group and the supportive therapy working group of the Italian Association of Pediatric Hematology and Oncology (AIEOP).
Giordano P, Saracco P, Grassi M, Luciani M, Banov L, Carraro F, Crocoli A, Cesaro S, Zanazzo GA, Molinari AC; Italian Association of Pediatric Hematology and Oncology (AIEOP). Giordano P, et al. Among authors: luciani m. Ann Hematol. 2015 Nov;94(11):1765-76. doi: 10.1007/s00277-015-2481-1. Epub 2015 Aug 25. Ann Hematol. 2015. PMID: 26300457 Review.
375 results