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

Year Number of Results
1954 1
1967 1
1976 1
1989 1
1991 2
1992 2
1993 6
1994 1
1995 4
1996 4
1997 4
1998 3
1999 3
2000 4
2001 8
2002 13
2003 10
2004 6
2005 9
2006 9
2007 9
2008 9
2009 8
2010 11
2011 7
2012 7
2013 4
2014 7
2015 11
2016 6
2017 2
2018 5
2019 4
2020 5
2021 3
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167 results
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Page 1
A tribute to Cecilio Romana: Romana's sign in Chagas disease.
Beucler N, Torrico F, Hibbert D. Beucler N, et al. PLoS Negl Trop Dis. 2020 Nov 12;14(11):e0008836. doi: 10.1371/journal.pntd.0008836. eCollection 2020 Nov. PLoS Negl Trop Dis. 2020. PMID: 33180778 Free PMC article. No abstract available.
Romana's sign.
Delaporte F. Delaporte F. J Hist Biol. 1997 Fall;30(3):357-66. doi: 10.1023/a:1004221722554. J Hist Biol. 1997. PMID: 11619786 No abstract available.
[Cecilio Romana, Romana's sign and Chagas' disease].
Dias JC. Dias JC. Rev Soc Bras Med Trop. 1997 Sep-Oct;30(5):407-13. doi: 10.1590/s0037-86821997000500012. Rev Soc Bras Med Trop. 1997. PMID: 9380903 Portuguese.
This description caused an enormous polemic with Romana's then director, the great Salvador Mazza, who never accepted the specificity of the sign and, much less, its popular name (which was proposed by the Brazilian researchers Emmanuel Dias and Evandro Chagas). Thi …
This description caused an enormous polemic with Romana's then director, the great Salvador Mazza, who never accepted the spec …
[Romana's sign].
PICK F. PICK F. Acta Trop. 1954;11(2):105-38. Acta Trop. 1954. PMID: 13197123 French. No abstract available.
Mutation in TET2 in myeloid cancers.
Delhommeau F, Dupont S, Della Valle V, James C, Trannoy S, Massé A, Kosmider O, Le Couedic JP, Robert F, Alberdi A, Lécluse Y, Plo I, Dreyfus FJ, Marzac C, Casadevall N, Lacombe C, Romana SP, Dessen P, Soulier J, Viguié F, Fontenay M, Vainchenker W, Bernard OA. Delhommeau F, et al. N Engl J Med. 2009 May 28;360(22):2289-301. doi: 10.1056/NEJMoa0810069. N Engl J Med. 2009. PMID: 19474426 Free article.
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.
Kim JH, Shinde DN, Reijnders MRF, Hauser NS, Belmonte RL, Wilson GR, Bosch DGM, Bubulya PA, Shashi V, Petrovski S, Stone JK, Park EY, Veltman JA, Sinnema M, Stumpel CTRM, Draaisma JM, Nicolai J; University of Washington Center for Mendelian Genomics, Yntema HG, Lindstrom K, de Vries BBA, Jewett T, Santoro SL, Vogt J; Deciphering Developmental Disorders Study, Bachman KK, Seeley AH, Krokosky A, Turner C, Rohena L, Hempel M, Kortüm F, Lessel D, Neu A, Strom TM, Wieczorek D, Bramswig N, Laccone FA, Behunova J, Rehder H, Gordon CT, Rio M, Romana S, Tang S, El-Khechen D, Cho MT, McWalter K, Douglas G, Baskin B, Begtrup A, Funari T, Schoch K, Stegmann APA, Stevens SJC, Zhang DE, Traver D, Yao X, MacArthur DG, Brunner HG, Mancini GM, Myers RM, Owen LB, Lim ST, Stachura DL, Vissers LELM, Ahn EYE. Kim JH, et al. Am J Hum Genet. 2016 Sep 1;99(3):711-719. doi: 10.1016/j.ajhg.2016.06.029. Epub 2016 Aug 18. Am J Hum Genet. 2016. PMID: 27545680 Free PMC article.
New insights into genotype-phenotype correlation for GLI3 mutations.
Démurger F, Ichkou A, Mougou-Zerelli S, Le Merrer M, Goudefroye G, Delezoide AL, Quélin C, Manouvrier S, Baujat G, Fradin M, Pasquier L, Megarbané A, Faivre L, Baumann C, Nampoothiri S, Roume J, Isidor B, Lacombe D, Delrue MA, Mercier S, Philip N, Schaefer E, Holder M, Krause A, Laffargue F, Sinico M, Amram D, André G, Liquier A, Rossi M, Amiel J, Giuliano F, Boute O, Dieux-Coeslier A, Jacquemont ML, Afenjar A, Van Maldergem L, Lackmy-Port-Lis M, Vincent-Delorme C, Chauvet ML, Cormier-Daire V, Devisme L, Geneviève D, Munnich A, Viot G, Raoul O, Romana S, Gonzales M, Encha-Razavi F, Odent S, Vekemans M, Attie-Bitach T. Démurger F, et al. Eur J Hum Genet. 2015 Jan;23(1):92-102. doi: 10.1038/ejhg.2014.62. Epub 2014 Apr 16. Eur J Hum Genet. 2015. PMID: 24736735 Free PMC article.
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1.
Hacein-Bey-Abina S, Von Kalle C, Schmidt M, McCormack MP, Wulffraat N, Leboulch P, Lim A, Osborne CS, Pawliuk R, Morillon E, Sorensen R, Forster A, Fraser P, Cohen JI, de Saint Basile G, Alexander I, Wintergerst U, Frebourg T, Aurias A, Stoppa-Lyonnet D, Romana S, Radford-Weiss I, Gross F, Valensi F, Delabesse E, Macintyre E, Sigaux F, Soulier J, Leiva LE, Wissler M, Prinz C, Rabbitts TH, Le Deist F, Fischer A, Cavazzana-Calvo M. Hacein-Bey-Abina S, et al. Science. 2003 Oct 17;302(5644):415-9. doi: 10.1126/science.1088547. Science. 2003. PMID: 14564000 Free article.
Comment on: Monogenic mimics of Behcet's disease in the young.
Aeschlimann FA, Stolzenberg MC, Rieux-Laucat F, Bustaffa M, Quartier P, Lyonnet S, Romana S, Bader-Meunier B. Aeschlimann FA, et al. Rheumatology (Oxford). 2020 Nov 1;59(11):e109-e111. doi: 10.1093/rheumatology/kez543. Rheumatology (Oxford). 2020. PMID: 31725163 No abstract available.
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