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Year Number of Results
1992 2
1993 4
1994 1
1995 1
1996 4
1997 2
2000 3
2001 1
2002 1
2003 4
2004 2
2005 4
2006 5
2007 3
2008 6
2009 2
2010 1
2011 4
2012 4
2013 8
2014 3
2015 7
2016 3
2017 1
2018 1
2019 2
2020 5
2021 8
2022 1
2023 2
2024 1

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90 results

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Page 1
Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review.
Ter Haar N, Lachmann H, Özen S, Woo P, Uziel Y, Modesto C, Koné-Paut I, Cantarini L, Insalaco A, Neven B, Hofer M, Rigante D, Al-Mayouf S, Touitou I, Gallizzi R, Papadopoulou-Alataki E, Martino S, Kuemmerle-Deschner J, Obici L, Iagaru N, Simon A, Nielsen S, Martini A, Ruperto N, Gattorno M, Frenkel J; Paediatric Rheumatology International Trials Organisation (PRINTO) and the Eurofever/Eurotraps Projects. Ter Haar N, et al. Ann Rheum Dis. 2013 May;72(5):678-85. doi: 10.1136/annrheumdis-2011-201268. Epub 2012 Jun 29. Ann Rheum Dis. 2013. PMID: 22753383 Free article. Review.
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory Syndrome.
Dotta L, Moratto D, Cattalini M, Brambilla S, Giustini V, Meini A, Girelli MF, Cortesi M, Timpano S, Galvagni A, Viola A, Crotti B, Manerba A, Pierelli G, Verzura G, Serana F, Brugnoni D, Garrafa E, Ricci F, Tomasi C, Chiarini M, Badolato R. Dotta L, et al. Among authors: meini a. Children (Basel). 2023 Jun 16;10(6):1069. doi: 10.3390/children10061069. Children (Basel). 2023. PMID: 37371300 Free PMC article.
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor 𝛋B kinase alpha (IKKα).
Bainter W, Lougaris V, Wallace JG, Badran Y, Hoyos-Bachiloglu R, Peters Z, Wilkie H, Das M, Janssen E, Beano A, Farhat KB, Kam C, Bercich L, Incardona P, Villanacci V, Bondioni MP, Meini A, Baronio M, Abarzua P, Parolini S, Tabellini G, Maio S, Schmidt B, Goldsmith JD, Murphy G, Hollander G, Plebani A, Chou J, Geha RS. Bainter W, et al. Among authors: meini a. Sci Immunol. 2021 Sep 17;6(63):eabf6723. doi: 10.1126/sciimmunol.abf6723. Epub 2021 Sep 17. Sci Immunol. 2021. PMID: 34533979 Free PMC article.
A Strange Manifestation of Malaria in a Native Nigerian Boy.
Magro P, Izzo I, Saccani B, Casari S, Caligaris S, Tomasoni LR, Matteelli A, Lombardi A, Meini A, Castelli F. Magro P, et al. Among authors: meini a. Mediterr J Hematol Infect Dis. 2017 Mar 1;9(1):e2017023. doi: 10.4084/MJHID.2017.023. eCollection 2017. Mediterr J Hematol Infect Dis. 2017. PMID: 28293411 Free PMC article.
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function.
Dotta L, Baresi G, Tamassia N, Calzetti F, Bianchetto-Aguilera F, Gasperini S, Gardiman E, Chiarini M, Moratto D, Martellosio G, Serana F, Micheletti M, Tregambe D, Pintabona V, Soncini E, Meini A, Girelli MF, Beghin A, Lanfranchi A, Bugatti M, Brugnoni D, Soresina A, Plebani A, Cassatella M, Vermi W, Porta F, Badolato R. Dotta L, et al. Among authors: meini a. Pediatr Blood Cancer. 2023 Dec;70(12):e30671. doi: 10.1002/pbc.30671. Epub 2023 Sep 15. Pediatr Blood Cancer. 2023. PMID: 37712719
A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children.
Gattorno M, Sormani MP, D'Osualdo A, Pelagatti MA, Caroli F, Federici S, Cecconi M, Solari N, Meini A, Zulian F, Obici L, Breda L, Martino S, Tommasini A, Bossi G, Govers A, Touitou I, Woo P, Frenkel J, Koné-Paut I, Baldi M, Ceccherini I, Martini A. Gattorno M, et al. Among authors: meini a. Arthritis Rheum. 2008 Jun;58(6):1823-32. doi: 10.1002/art.23474. Arthritis Rheum. 2008. PMID: 18512793 Free article.
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis.
Galli J, Gavazzi F, De Simone M, Giliani S, Garau J, Valente M, Vairo D, Cattalini M, Mortilla M, Andreoli L, Badolato R, Bianchi M, Carabellese N, Cereda C, Ferraro R, Facchetti F, Fredi M, Gualdi G, Lorenzi L, Meini A, Orcesi S, Tincani A, Zanola A, Rice G, Fazzi E; AGS study group. Galli J, et al. Among authors: meini a. Medicine (Baltimore). 2018 Dec;97(52):e13893. doi: 10.1097/MD.0000000000013893. Medicine (Baltimore). 2018. PMID: 30593198 Free PMC article.
Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ.
Lougaris V, Baronio M, Castagna A, Tessarin G, Rossi S, Gazzurelli L, Benvenuto A, Moratto D, Chiarini M, Cattalini M, Facchetti M, Palumbo L, Giliani S, Girelli MF, Badolato R, Bondioni MP, Facchetti F, Meini A, Plebani A. Lougaris V, et al. Among authors: meini a. Clin Immunol. 2020 Oct;219:108543. doi: 10.1016/j.clim.2020.108543. Epub 2020 Jul 16. Clin Immunol. 2020. PMID: 32681977
90 results