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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 1
1986 2
1987 1
1988 3
1991 4
1993 4
1994 1
1995 2
1996 5
1997 5
1998 9
1999 4
2000 4
2001 3
2002 8
2003 2
2004 4
2005 5
2006 4
2007 6
2008 6
2009 1
2010 3
2011 3
2012 3
2013 5
2014 5
2015 1
2016 1
2017 1
2024 0

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98 results

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Page 1
EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria.
Ozen S, Pistorio A, Iusan SM, Bakkaloglu A, Herlin T, Brik R, Buoncompagni A, Lazar C, Bilge I, Uziel Y, Rigante D, Cantarini L, Hilario MO, Silva CA, Alegria M, Norambuena X, Belot A, Berkun Y, Estrella AI, Olivieri AN, Alpigiani MG, Rumba I, Sztajnbok F, Tambic-Bukovac L, Breda L, Al-Mayouf S, Mihaylova D, Chasnyk V, Sengler C, Klein-Gitelman M, Djeddi D, Nuno L, Pruunsild C, Brunner J, Kondi A, Pagava K, Pederzoli S, Martini A, Ruperto N; Paediatric Rheumatology International Trials Organisation (PRINTO). Ozen S, et al. Among authors: buoncompagni a. Ann Rheum Dis. 2010 May;69(5):798-806. doi: 10.1136/ard.2009.116657. Ann Rheum Dis. 2010. PMID: 20413568
Osteopetrorickets: case report.
Di Rocco M, Buoncompagni A, Loy A, Dellacqua A. Di Rocco M, et al. Among authors: buoncompagni a. Eur J Pediatr. 2000 Aug;159(8):579-81. doi: 10.1007/s004310000485. Eur J Pediatr. 2000. PMID: 10968234
Severe hypoalbuminaemia in a systemic lupus erythematosus-like patient.
Gattorno M, Buoncompagni A, Barabino A, Barbano G, Loy A, Tomà P, Picco P, Marmont AM. Gattorno M, et al. Among authors: buoncompagni a. Eur J Pediatr. 2002 Feb;161(2):84-6. doi: 10.1007/s00431-001-0868-6. Eur J Pediatr. 2002. PMID: 11954757 Review.
Childhood systemic lupus erythematosus: a review of 30 cases.
Buoncompagni A, Barbano GC, Pistoia V, Fasce L, Micalizzi C, Gusmano R, Cordone G, Cottafava F, Mori PG, Franchini E, et al. Buoncompagni A, et al. Clin Exp Rheumatol. 1991 Jul-Aug;9(4):425-30. Clin Exp Rheumatol. 1991. PMID: 1934695 Review.
Clinical overview and outcome in a cohort of children with polyarteritis nodosa.
Falcini F, La Torre F, Vittadello F, Rigante D, Martini G, Corona F, Buoncompagni A, Alessio M, Cortis E, Insalaco A, Magni-Manzoni S, Breda L, Matucci-Cerinic M, Zulian F. Falcini F, et al. Among authors: buoncompagni a. Clin Exp Rheumatol. 2014 May-Jun;32(3 Suppl 82):S134-7. Epub 2014 Feb 11. Clin Exp Rheumatol. 2014. PMID: 24529184
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay.
Volpi S, Yamazaki Y, Brauer PM, van Rooijen E, Hayashida A, Slavotinek A, Sun Kuehn H, Di Rocco M, Rivolta C, Bortolomai I, Du L, Felgentreff K, Ott de Bruin L, Hayashida K, Freedman G, Marcovecchio GE, Capuder K, Rath P, Luche N, Hagedorn EJ, Buoncompagni A, Royer-Bertrand B, Giliani S, Poliani PL, Imberti L, Dobbs K, Poulain FE, Martini A, Manis J, Linhardt RJ, Bosticardo M, Rosenzweig SD, Lee H, Puck JM, Zúñiga-Pflücker JC, Zon L, Park PW, Superti-Furga A, Notarangelo LD. Volpi S, et al. Among authors: buoncompagni a. J Exp Med. 2017 Mar 6;214(3):623-637. doi: 10.1084/jem.20161525. Epub 2017 Feb 1. J Exp Med. 2017. PMID: 28148688 Free PMC article.
Recurrent pericarditis in Myhre syndrome.
Picco P, Naselli A, Pala G, Marsciani A, Buoncompagni A, Martini A. Picco P, et al. Among authors: buoncompagni a. Am J Med Genet A. 2013 May;161A(5):1164-6. doi: 10.1002/ajmg.a.35892. Am J Med Genet A. 2013. PMID: 23610053
Childhood thalidomide neuropathy: a clinical and neurophysiologic study.
Priolo T, Lamba LD, Giribaldi G, De Negri E, Grosso P, De Grandis E, Veneselli E, Buoncompagni A, Viola S, Alpigiani MG, Gandullia P, Calevo MG. Priolo T, et al. Among authors: buoncompagni a. Pediatr Neurol. 2008 Mar;38(3):196-9. doi: 10.1016/j.pediatrneurol.2007.11.004. Pediatr Neurol. 2008. PMID: 18279755 Clinical Trial.
98 results