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Rapid complete blood count and C-reactive protein determination with the Horiba Microsemi analyzer: the experience in neonatal intensive care unit of Careggi University Hospital.
Nencini F, Bonari A, Romano F, Ciullini Mannurita S, Mongia A, Garieri M, Dani C, Manzo O, Pontieri M, Fanelli A
Eur J Pediatr, 183(10):4477-4490, 15 Aug 2024
Cited by: 0 articles | PMID: 39143348 | PMCID: PMC11413159
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A Rare Onset of T-Lymphoid Blast Crisis in Chronic Myeloid Leukemia with Two Distinct Blast Populations.
Mongia A, Romano F, Ciullini Mannurita S, Peruzzi B, Bencini S, Parrini D, Fasano L, Fanelli A
Hematol Rep, 16(3):413-420, 27 Jun 2024
Cited by: 0 articles | PMID: 39051413 | PMCID: PMC11431131
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A Rare Onset of T Lymphoid Blast Crisis in Chronic Myeloid Leukemia with Two Distinct Blast Populations
Mongia A, Romano F, Ciullini Mannurita S, Peruzzi B, Bencini S, Parrini D, Fasano L, Fanelli A
Preprints.org, 27 Mar 2024
Cited by: 0 articles | PPR: PPR830146
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β3-adrenergic receptor on tumor-infiltrating lymphocytes sustains IFN-γ-dependent PD-L1 expression and impairs anti-tumor immunity in neuroblastoma.
Bruno G, Nastasi N, Subbiani A, Boaretto A, Ciullini Mannurita S, Mattei G, Nardini P, Della Bella C, Magi A, Pini A, De Marco E, Tondo A, Favre C, Calvani M
Cancer Gene Ther, 30(6):890-904, 28 Feb 2023
Cited by: 7 articles | PMID: 36854895 | PMCID: PMC10281870
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Autoimmune Cytopenias and Dysregulated Immunophenotype Act as Warning Signs of Inborn Errors of Immunity: Results From a Prospective Study.
Schiavo E, Martini B, Attardi E, Consonni F, Ciullini Mannurita S, Coniglio ML, Tellini M, Chiocca E, Fotzi I, Luti L, D'Alba I, Veltroni M, Favre C, Gambineri E
Front Immunol, 12:790455, 04 Jan 2022
Cited by: 11 articles | PMID: 35058929 | PMCID: PMC8765341
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Case Report: Signal Transducer and Activator of Transcription 3 Gain-of-Function and Spectrin Deficiency: A Life-Threatening Case of Severe Hemolytic Anemia.
Ciullini Mannurita S, Goda R, Schiavo E, Coniglio ML, Azzali A, Fotzi I, Tondo A, Tintori V, Frenos S, Sanvito MC, Vignoli M, Luceri C, Bigagli E, Grassi A, D'Elios MM, Favre C, Gambineri E
Front Immunol, 11:620046, 15 Jan 2021
Cited by: 5 articles | PMID: 33519826 | PMCID: PMC7843414
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Atypical Presentations of IPEX: Expect the Unexpected.
Consonni F, Ciullini Mannurita S, Gambineri E
Front Pediatr, 9:643094, 05 Feb 2021
Cited by: 22 articles | PMID: 33614561 | PMCID: PMC7892580
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β3-Adrenoceptors as Putative Regulator of Immune Tolerance in Cancer and Pregnancy.
Calvani M, Dabraio A, Subbiani A, Buonvicino D, De Gregorio V, Ciullini Mannurita S, Pini A, Nardini P, Favre C, Filippi L
Front Immunol, 11:2098, 02 Sep 2020
Cited by: 12 articles | PMID: 32983164 | PMCID: PMC7492666
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CD25 deficiency: A new conformational mutation prevents the receptor expression on cell surface.
Vignoli M, Ciullini Mannurita S, Fioravanti A, Tumino M, Grassi A, Guariso G, Favre C, D'Elios MM, Gambineri E
Clin Immunol, 201:15-19, 08 Feb 2019
Cited by: 11 articles | PMID: 30742970
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Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.
Gambineri E, Ciullini Mannurita S, Hagin D, Vignoli M, Anover-Sombke S, DeBoer S, Segundo GRS, Allenspach EJ, Favre C, Ochs HD, Torgerson TR
Front Immunol, 9:2411, 01 Nov 2018
Cited by: 81 articles | PMID: 30443250 | PMCID: PMC6223101
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Novel molecular defects associated with very early-onset inflammatory bowel.
Ciullini Mannurita S, Gambineri E
Curr Opin Allergy Clin Immunol, 17(5):317-324, 01 Oct 2017
Cited by: 2 articles | PMID: 28817385
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Timely follow-up of a GATA2 deficiency patient allows successful treatment.
Ciullini Mannurita S, Vignoli M, Colarusso G, Tucci F, Veltroni M, Frenos S, Tintori V, Aricò M, Bigley V, Collin M, Favre C, Gambineri E
J Allergy Clin Immunol, 138(5):1480-1483.e4, 29 Jul 2016
Cited by: 8 articles | PMID: 27481672
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Gut immune reconstitution in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome after hematopoietic stem cell transplantation.
Gambineri E, Ciullini Mannurita S, Robertson H, Vignoli M, Haugk B, Lionetti P, Hambleton S, Barge D, Gennery AR, Slatter M, Nademi Z, Flood TJ, Jackson A, Abinun M, Cant AJ
J Allergy Clin Immunol, 135(1):260-262, 25 Oct 2014
Cited by: 7 articles | PMID: 25420685 | PMCID: PMC4282727
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CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort.
Ciullini Mannurita S, Vignoli M, Bianchi L, Kondi A, Gerloni V, Breda L, Ten Cate R, Alessio M, Ravelli A, Falcini F, Gambineri E
Eur J Hum Genet, 22(2):197-201, 12 Jun 2013
Cited by: 16 articles | PMID: 23756439 | PMCID: PMC3895642
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Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity.
Goudy K, Aydin D, Barzaghi F, Gambineri E, Vignoli M, Ciullini Mannurita S, Doglioni C, Ponzoni M, Cicalese MP, Assanelli A, Tommasini A, Brigida I, Dellepiane RM, Martino S, Olek S, Aiuti A, Ciceri F, Roncarolo MG, Bacchetta R
Clin Immunol, 146(3):248-261, 24 Jan 2013
Cited by: 111 articles | PMID: 23416241 | PMCID: PMC3594590
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Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome.
Barzaghi F, Passerini L, Gambineri E, Ciullini Mannurita S, Cornu T, Kang ES, Choe YH, Cancrini C, Corrente S, Ciccocioppo R, Cecconi M, Zuin G, Discepolo V, Sartirana C, Schmidtko J, Ikinciogullari A, Ambrosi A, Roncarolo MG, Olek S, Bacchetta R
J Autoimmun, 38(1):49-58, 20 Jan 2012
Cited by: 47 articles | PMID: 22264504 | PMCID: PMC3314976
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