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Page 1
Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.
Geier CB, Ellison M, Cruz R, Pawar S, Leiss-Piller A, Zmajkovicova K, McNulty SM, Yilmaz M, Evans MO 2nd, Gordon S, Ujhazi B, Wiest I, Abolhassani H, Aghamohammadi A, Barmettler S, Bhar S, Bondarenko A, Bolyard AA, Buchbinder D, Cada M, Cavieres M, Connelly JA, Dale DC, Deordieva E, Dorsey MJ, Drysdale SB, Ehl S, Elfeky R, Fioredda F, Firkin F, Förster-Waldl E, Geng B, Goda V, Gonzalez-Granado L, Grunebaum E, Grzesk E, Henrickson SE, Hilfanova A, Hiwatari M, Imai C, Ip W, Jyonouchi S, Kanegane H, Kawahara Y, Khojah AM, Kim VH, Kojić M, Kołtan S, Krivan G, Langguth D, Lau YL, Leung D, Miano M, Mersyanova I, Mousallem T, Muskat M, Naoum FA, Noronha SA, Ouederni M, Ozono S, Richmond GW, Sakovich I, Salzer U, Schuetz C, Seeborg FO, Sharapova SO, Sockel K, Volokha A, von Bonin M, Warnatz K, Wegehaupt O, Weinberg GA, Wong KJ, Worth A, Yu H, Zharankova Y, Zhao X, Devlin L, Badarau A, Csomos K, Keszei M, Pereira J, Taveras AG, Beaussant-Cohen SL, Ong MS, Shcherbina A, Walter JE. Geier CB, et al. Among authors: fioredda f. J Clin Immunol. 2022 Nov;42(8):1748-1765. doi: 10.1007/s10875-022-01312-7. Epub 2022 Aug 10. J Clin Immunol. 2022. PMID: 35947323 Free PMC article.
Old and new faces of neutropenia in children.
Dufour C, Miano M, Fioredda F. Dufour C, et al. Among authors: fioredda f. Haematologica. 2016 Jul;101(7):789-91. doi: 10.3324/haematol.2016.142760. Haematologica. 2016. PMID: 27365457 Free PMC article. No abstract available.
RAG deficiency with ALPS features successfully treated with TCRαβ/CD19 cell depleted haploidentical stem cell transplant.
Westermann-Clark E, Grossi A, Fioredda F, Giardino S, Cappelli E, Terranova P, Palmisani E, Farmer JR, Foldvari Z, Yamazaki Y, Faraci M, Lanino E, Notarangelo LD, Dufour C, Ceccherini I, Walter JE, Miano M. Westermann-Clark E, et al. Among authors: fioredda f. Clin Immunol. 2018 Feb;187:102-103. doi: 10.1016/j.clim.2017.10.012. Epub 2017 Nov 20. Clin Immunol. 2018. PMID: 29104089 Free PMC article. No abstract available.
Targeted NGS Yields Plentiful Ultra-Rare Variants in Inborn Errors of Immunity Patients.
Grossi A, Miano M, Lanciotti M, Fioredda F, Guardo D, Palmisani E, Terranova P, Santamaria G, Caroli F, Caorsi R, Volpi S, Gattorno M, Dufour C, Ceccherini I. Grossi A, et al. Among authors: fioredda f. Genes (Basel). 2021 Aug 24;12(9):1299. doi: 10.3390/genes12091299. Genes (Basel). 2021. PMID: 34573280 Free PMC article.
Case Report: Deficiency of Adenosine Deaminase 2 Presenting With Overlapping Features of Autoimmune Lymphoproliferative Syndrome and Bone Marrow Failure.
Dell'Orso G, Grossi A, Penco F, Caorsi R, Palmisani E, Terranova P, Schena F, Lupia M, Ricci E, Montalto S, Pierri F, Ceccherini I, Fioredda F, Dufour C, Gattorno M, Miano M. Dell'Orso G, et al. Among authors: fioredda f. Front Immunol. 2021 Oct 14;12:754029. doi: 10.3389/fimmu.2021.754029. eCollection 2021. Front Immunol. 2021. PMID: 34721429 Free PMC article.
Underlying Inborn Errors of Immunity in Patients With Evans Syndrome and Multilineage Cytopenias: A Single-Centre Analysis.
Miano M, Guardo D, Grossi A, Palmisani E, Fioredda F, Terranova P, Cappelli E, Lupia M, Traverso M, Dell'Orso G, Corsolini F, Beccaria A, Lanciotti M, Ceccherini I, Dufour C. Miano M, et al. Among authors: fioredda f. Front Immunol. 2022 May 17;13:869033. doi: 10.3389/fimmu.2022.869033. eCollection 2022. Front Immunol. 2022. PMID: 35655776 Free PMC article.
Autoimmune Neutropenia and Immune-Dysregulation in a Patient Carrying a TINF2 Variant.
Chianucci B, Grossi A, Dell'Orso G, Palmisani E, Lanciotti M, Terranova P, Pierri F, Lupia M, Arcuri L, Laurino M, Ceccherini I, Beier F, Dufour C, Fioredda F, Miano M. Chianucci B, et al. Among authors: fioredda f. Int J Mol Sci. 2022 Nov 22;23(23):14535. doi: 10.3390/ijms232314535. Int J Mol Sci. 2022. PMID: 36498862 Free PMC article.
COVID-19 disease in patients with chronic neutropenia: The experience from the European Network for Innovative Diagnosis and Treatment of Chronic Neutropenias.
Spanoudakis M, Yilmaz Karapinar D, Dale D, Bolyard AA, Tran E, Roganovic J, Bartels M, Kapor S, Guardo D, Yacobovich J, Nilsson C, Bezzerri V, Cipolli M, Pegoraro A, Aleksov E, Guenova M, Dufour C, Fioredda F, Papadaki HA, Palmblad J. Spanoudakis M, et al. Among authors: fioredda f. Br J Haematol. 2024 Mar 20. doi: 10.1111/bjh.19411. Online ahead of print. Br J Haematol. 2024. PMID: 38506338 No abstract available.
Diagnostic potential of hepcidin testing in pediatrics.
Cangemi G, Pistorio A, Miano M, Gattorno M, Acquila M, Bicocchi MP, Gastaldi R, Riccardi F, Gatti C, Fioredda F, Calvillo M, Melioli G, Martini A, Dufour C. Cangemi G, et al. Among authors: fioredda f. Eur J Haematol. 2013 Apr;90(4):323-30. doi: 10.1111/ejh.12081. Epub 2013 Feb 26. Eur J Haematol. 2013. PMID: 23438060
86 results