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Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian Association of Pediatric Hematology-Oncology).
Svahn J, Bagnasco F, Cappelli E, Onofrillo D, Caruso S, Corsolini F, De Rocco D, Savoia A, Longoni D, Pillon M, Marra N, Ramenghi U, Farruggia P, Locasciulli A, Addari C, Cerri C, Mastrodicasa E, Casazza G, Verzegnassi F, Riccardi F, Haupt R, Barone A, Cesaro S, Cugno C, Dufour C. Svahn J, et al. Among authors: cappelli e. Am J Hematol. 2016 Jul;91(7):666-71. doi: 10.1002/ajh.24373. Epub 2016 Apr 24. Am J Hematol. 2016. PMID: 27013026 Free article.
Genetic screening of children with marrow failure. The role of primary Immunodeficiencies.
Miano M, Grossi A, Dell'Orso G, Lanciotti M, Fioredda F, Palmisani E, Lanza T, Guardo D, Beccaria A, Ravera S, Cossu V, Terranova P, Giona F, Santopietro M, Cappelli E, Ceccherini I, Dufour C. Miano M, et al. Among authors: cappelli e. Am J Hematol. 2021 Sep 1;96(9):1077-1086. doi: 10.1002/ajh.26242. Epub 2021 Jun 2. Am J Hematol. 2021. PMID: 34000087 Free article.
Immunological profile of Fanconi anemia: a multicentric retrospective analysis of 61 patients.
Korthof ET, Svahn J, Peffault de Latour R, Terranova P, Moins-Teisserenc H, Socié G, Soulier J, Kok M, Bredius RG, van Tol M, Jol-van der Zijde EC, Pistorio A, Corsolini F, Parodi A, Battaglia F, Pistoia V, Dufour C, Cappelli E. Korthof ET, et al. Among authors: cappelli e. Am J Hematol. 2013 Jun;88(6):472-6. doi: 10.1002/ajh.23435. Epub 2013 May 2. Am J Hematol. 2013. PMID: 23483621 Free article.
Sirolimus as a rescue therapy in children with immune thrombocytopenia refractory to mycophenolate mofetil.
Miano M, Rotulo GA, Palmisani E, Giaimo M, Fioredda F, Pierri F, Pezzulla A, Licciardello M, Terranova P, Lanza T, Cappelli E, Maggiore R, Calvillo M, Micalizzi C, Russo G, Dufour C. Miano M, et al. Among authors: cappelli e. Am J Hematol. 2018 Jul;93(7):E175-E177. doi: 10.1002/ajh.25119. Epub 2018 May 6. Am J Hematol. 2018. PMID: 29675829 Free article. No abstract available.
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.
De Rocco D, Bottega R, Cappelli E, Cavani S, Criscuolo M, Nicchia E, Corsolini F, Greco C, Borriello A, Svahn J, Pillon M, Mecucci C, Casazza G, Verzegnassi F, Cugno C, Locasciulli A, Farruggia P, Longoni D, Ramenghi U, Barberi W, Tucci F, Perrotta S, Grammatico P, Hanenberg H, Della Ragione F, Dufour C, Savoia A; Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. De Rocco D, et al. Among authors: cappelli e. Haematologica. 2014 Jun;99(6):1022-31. doi: 10.3324/haematol.2014.104224. Epub 2014 Feb 28. Haematologica. 2014. PMID: 24584348 Free PMC article.
Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing.
Nicchia E, Benedicenti F, De Rocco D, Greco C, Bottega R, Inzana F, Faleschini M, Bonin S, Cappelli E, Mogni M, Stanzial F, Svahn J, Dufour C, Savoia A. Nicchia E, et al. Among authors: cappelli e. Birth Defects Res A Clin Mol Teratol. 2015 Dec;103(12):1003-10. doi: 10.1002/bdra.23388. Epub 2015 Jun 2. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26033879
Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology.
Nicchia E, Greco C, De Rocco D, Pecile V, D'Eustacchio A, Cappelli E, Corti P, Marra N, Ramenghi U, Pillon M, Farruggia P, Dufour C, Pallavicini A, Torelli L, Savoia A. Nicchia E, et al. Among authors: cappelli e. Mol Genet Genomic Med. 2015 Jul 2;3(6):500-12. doi: 10.1002/mgg3.160. eCollection 2015 Nov. Mol Genet Genomic Med. 2015. PMID: 26740942 Free PMC article.
119 results