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Page 1
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group.
Corti P, Ferrari GM, Faraguna MC, Capitoli G, Longo F, Corradini E, Casini T, Boscarol G, Pinto VM, Ghilardi R, Russo G, Colombatti R, Mariani R, Piperno A. Corti P, et al. Among authors: russo g. Br J Haematol. 2024 Jan;204(1):306-314. doi: 10.1111/bjh.19208. Epub 2023 Nov 21. Br J Haematol. 2024. PMID: 37990447
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort.
Randi ML, Geranio G, Bertozzi I, Micalizzi C, Ramenghi U, Tucci F, Notarangelo LD, Ladogana S, Menna G, Giordano P, Consarino C, Farruggia P, Zanazzo GA, Fiori GM, Burnelli R, Russo G, Jankovich M, Peroni E, Duner E, Basso G, Fabris F, Putti MC. Randi ML, et al. Among authors: russo g. Br J Haematol. 2015 May;169(4):584-9. doi: 10.1111/bjh.13329. Epub 2015 Feb 25. Br J Haematol. 2015. PMID: 25716342 Free article. Clinical Trial.
Pearson Syndrome: A Retrospective Cohort Study from the Marrow Failure Study Group of A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica).
Farruggia P, Di Cataldo A, Pinto RM, Palmisani E, Macaluso A, Valvo LL, Cantarini ME, Tornesello A, Corti P, Fioredda F, Varotto S, Martire B, Moroni I, Puccio G, Russo G, Dufour C, Pillon M. Farruggia P, et al. Among authors: russo g. JIMD Rep. 2016;26:37-43. doi: 10.1007/8904_2015_470. Epub 2015 Aug 4. JIMD Rep. 2016. PMID: 26238250 Free PMC article.
Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: a retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica).
Farruggia P, Puccio G, Ramenghi U, Colombatti R, Corti P, Trizzino A, Barone A, Boscarol G, Ferraro F, Grotto P, Lo Valvo L, Luti L, Matarese SMR, Mosa C, Putti MC, Rubert L, Ruffo GB, Sainati L, Tartaglione I, Russo G, Perrotta S. Farruggia P, et al. Among authors: russo g. Am J Hematol. 2017 Jun;92(6):E103-E105. doi: 10.1002/ajh.24713. Epub 2017 Apr 26. Am J Hematol. 2017. PMID: 28263406 Free article. No abstract available.
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey.
Colombatti R, Palazzi G, Masera N, Notarangelo LD, Bonetti E, Samperi P, Barone A, Perrotta S, Facchini E, Miano M, Del Vecchio GC, Guerzoni ME, Corti P, Menzato F, Cesaro S, Casale M, Rigano P, Forni GL, Russo G, Sainati L; Italian Multicenter Study of Hydroxyurea in Sickle Cell Anemia Investigators. Colombatti R, et al. Among authors: russo g. Pediatr Blood Cancer. 2018 Feb;65(2). doi: 10.1002/pbc.26774. Epub 2017 Sep 4. Pediatr Blood Cancer. 2018. PMID: 28868627
Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP).
Ladogana S, Maruzzi M, Samperi P, Condorelli A, Casale M, Giordano P, Notarangelo LD, Farruggia P, Giona F, Nocerino A, Fasoli S, Casciana ML, Miano M, Tucci F, Casini T, Saracco P, Barcellini W, Zanella A, Perrotta S, Russo G; AIHA Committee of the Associazione Italiana di Ematologia ed Oncologia Pediatrica. Ladogana S, et al. Among authors: russo g. Blood Transfus. 2018 Jul;16(4):352-357. doi: 10.2450/2018.0024-18. Epub 2018 Apr 13. Blood Transfus. 2018. PMID: 29757134 Free PMC article. No abstract available.
Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.
Lobitz S, Telfer P, Cela E, Allaf B, Angastiniotis M, Backman Johansson C, Badens C, Bento C, Bouva MJ, Canatan D, Charlton M, Coppinger C, Daniel Y, de Montalembert M, Ducoroy P, Dulin E, Fingerhut R, Frömmel C, García-Morin M, Gulbis B, Holtkamp U, Inusa B, James J, Kleanthous M, Klein J, Kunz JB, Langabeer L, Lapouméroulie C, Marcao A, Marín Soria JL, McMahon C, Ohene-Frempong K, Périni JM, Piel FB, Russo G, Sainati L, Schmugge M, Streetly A, Tshilolo L, Turner C, Venturelli D, Vilarinho L, Yahyaoui R, Elion J, Colombatti R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Haematological Diseases. Lobitz S, et al. Among authors: russo g. Br J Haematol. 2018 Nov;183(4):648-660. doi: 10.1111/bjh.15600. Epub 2018 Oct 18. Br J Haematol. 2018. PMID: 30334577 Free article.
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry.
Farruggia P, Fioredda F, Puccio G, Onofrillo D, Russo G, Barone A, Bonanomi S, Boscarol G, Finocchi A, Ghilardi R, Giordano P, Ladogana S, Lassandro G, Luti L, Lanza T, Mandaglio R, Marra N, Martire B, Mastrodicasa E, Motta M, Notarangelo LD, Pillon M, Porretti L, Serafinelli J, Trizzino A, Tucci F, Veltroni M, Verzegnassi F, Ramenghi U, Dufour C. Farruggia P, et al. Among authors: russo g. Am J Hematol. 2019 Feb;94(2):216-222. doi: 10.1002/ajh.25353. Epub 2018 Dec 18. Am J Hematol. 2019. PMID: 30456824 Free article.
Current challenges in the management of patients with sickle cell disease - A report of the Italian experience.
Russo G, De Franceschi L, Colombatti R, Rigano P, Perrotta S, Voi V, Palazzi G, Fidone C, Quota A, Graziadei G, Pietrangelo A, Pinto V, Ruffo GB, Sorrentino F, Venturelli D, Casale M, Ferrara F, Sainati L, Cappellini MD, Piga A, Maggio A, Forni GL. Russo G, et al. Orphanet J Rare Dis. 2019 May 30;14(1):120. doi: 10.1186/s13023-019-1099-0. Orphanet J Rare Dis. 2019. PMID: 31146777 Free PMC article. Review.
HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation.
Notarangelo LD, Agostini A, Casale M, Samperi P, Arcioni F, Gorello P, Perrotta S, Masera N, Barone A, Bertoni E, Bonetti E, Burnelli R, Casini T, Del Vecchio GC, Filippini B, Giona F, Giordano P, Gorio C, Marchina E, Nardi M, Petrone A, Colombatti R, Sainati L, Russo G. Notarangelo LD, et al. Among authors: russo g. Eur J Haematol. 2020 Mar;104(3):214-222. doi: 10.1111/ejh.13362. Epub 2019 Dec 12. Eur J Haematol. 2020. PMID: 31788855
3,201 results