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Page 1
Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?
Palmisani E, Miano M, Grossi A, Lanciotti M, Lupia M, Terranova P, Ceccherini I, Montanari E, Calvillo M, Pierri F, Micalizzi C, Maggiore R, Guardo D, Zanardi S, Facchini E, Maggio A, Mastrodicasa E, Corti P, Russo G, Pillon M, Farruggia P, Cesaro S, Barone A, Tosetti F, Ramenghi U, Crescenzio N, Bleesing J, Dufour C, Fioredda F. Palmisani E, et al. Among authors: guardo d. Hemasphere. 2023 Feb 22;7(3):e845. doi: 10.1097/HS9.0000000000000845. eCollection 2023 Mar. Hemasphere. 2023. PMID: 36844186 Free PMC article.
FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene.
Miano M, Cappelli E, Pezzulla A, Venè R, Grossi A, Terranova P, Palmisani E, Maggiore R, Guardo D, Lanza T, Calvillo M, Micalizzi C, Pierri F, Vernarecci C, Beccaria A, Corsolini F, Lanciotti M, Russo G, Ceccherini I, Dufour C, Fioredda F. Miano M, et al. Among authors: guardo d. Br J Haematol. 2019 Nov;187(4):502-508. doi: 10.1111/bjh.16098. Epub 2019 Jul 15. Br J Haematol. 2019. PMID: 31309545 Free article.
Unusual Late-onset Enteropathy in a Patient With Lipopolysaccharide-responsive Beige-like Anchor Protein Deficiency.
Maggiore R, Grossi A, Fioredda F, Palmisani E, Terranova P, Cappelli E, Lanza T, Pierri F, Guardo D, Calvillo M, Micalizzi C, Beccaria A, Coccia MC, Arrigo S, Dufour C, Ceccherini I, Miano M. Maggiore R, et al. Among authors: guardo d. J Pediatr Hematol Oncol. 2020 Nov;42(8):e768-e771. doi: 10.1097/MPH.0000000000001708. J Pediatr Hematol Oncol. 2020. PMID: 31876783
Underlying CTLA4 Deficiency in a Patient With Juvenile Idiopathic Arthritis and Autoimmune Lymphoproliferative Syndrome Features Successfully Treated With Abatacept-A Case Report.
Mazzoni M, Dell'Orso G, Grossi A, Ceccherini I, Viola S, Terranova P, Micalizzi C, Guardo D, Massaccesi E, Palmisani E, Calvillo M, Fioredda F, Malattia C, Dufour C, Ravelli A, Miano M. Mazzoni M, et al. Among authors: guardo d. J Pediatr Hematol Oncol. 2021 Nov 1;43(8):e1168-e1172. doi: 10.1097/MPH.0000000000002120. J Pediatr Hematol Oncol. 2021. PMID: 33625086
The challenge of early diagnosis of autoimmune lymphoproliferative syndrome in children with suspected autoinflammatory/autoimmune disorders.
Oliveira Mendonça L, Matucci-Cerinic C, Terranova P, Casabona F, Bovis F, Caorsi R, Fioredda F, Palmisani E, Grossi A, Guardo D, Bustaffa M, Volpi S, Ceccherini I, Ravelli A, Dufour C, Miano M, Gattorno M. Oliveira Mendonça L, et al. Among authors: guardo d. Rheumatology (Oxford). 2022 Feb 2;61(2):696-704. doi: 10.1093/rheumatology/keab361. Rheumatology (Oxford). 2022. PMID: 33909886
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: guardo d. 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.
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: guardo d. Genes (Basel). 2021 Aug 24;12(9):1299. doi: 10.3390/genes12091299. Genes (Basel). 2021. PMID: 34573280 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: guardo d. Front Immunol. 2022 May 17;13:869033. doi: 10.3389/fimmu.2022.869033. eCollection 2022. Front Immunol. 2022. PMID: 35655776 Free PMC article.
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