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

Year Number of Results
1988 1
1996 1
1998 2
1999 3
2000 4
2001 1
2002 1
2003 2
2004 6
2005 6
2006 3
2007 10
2008 11
2009 12
2010 15
2011 9
2012 8
2013 12
2014 6
2015 8
2016 3
2017 5
2018 6
2019 9
2020 8
2021 7
2022 5
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144 results
Results by year
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Page 1
Diagnosing and managing bronchiolitis obliterans in children.
Kavaliunaite E, Aurora P. Kavaliunaite E, et al. Among authors: aurora p. Expert Rev Respir Med. 2019 May;13(5):481-488. doi: 10.1080/17476348.2019.1586537. Epub 2019 Mar 8. Expert Rev Respir Med. 2019. PMID: 30798629 Review.
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Project Pilot Investigators, et al. Among authors: aurora p. N Engl J Med. 2021 Nov 11;385(20):1868-1880. doi: 10.1056/NEJMoa2035790. N Engl J Med. 2021. PMID: 34758253
Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort.
Fassad MR, Patel MP, Shoemark A, Cullup T, Hayward J, Dixon M, Rogers AV, Ollosson S, Jackson C, Goggin P, Hirst RA, Rutman A, Thompson J, Jenkins L, Aurora P, Moya E, Chetcuti P, O'Callaghan C, Morris-Rosendahl DJ, Watson CM, Wilson R, Carr S, Walker W, Pitno A, Lopes S, Morsy H, Shoman W, Pereira L, Constant C, Loebinger MR, Chung EMK, Kenia P, Rumman N, Fasseeh N, Lucas JS, Hogg C, Mitchison HM. Fassad MR, et al. Among authors: aurora p. J Med Genet. 2020 May;57(5):322-330. doi: 10.1136/jmedgenet-2019-106501. Epub 2019 Dec 25. J Med Genet. 2020. PMID: 31879361
An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children.
Beydon N, Davis SD, Lombardi E, Allen JL, Arets HG, Aurora P, Bisgaard H, Davis GM, Ducharme FM, Eigen H, Gappa M, Gaultier C, Gustafsson PM, Hall GL, Hantos Z, Healy MJ, Jones MH, Klug B, Lødrup Carlsen KC, McKenzie SA, Marchal F, Mayer OH, Merkus PJ, Morris MG, Oostveen E, Pillow JJ, Seddon PC, Silverman M, Sly PD, Stocks J, Tepper RS, Vilozni D, Wilson NM; American Thoracic Society/European Respiratory Society Working Group on Infant and Young Children Pulmonary Function Testing. Beydon N, et al. Among authors: aurora p. Am J Respir Crit Care Med. 2007 Jun 15;175(12):1304-45. doi: 10.1164/rccm.200605-642ST. Am J Respir Crit Care Med. 2007. PMID: 17545458 Review. No abstract available.
Paediatrics in Amsterdam.
Eber E, Aurora P, Lødrup Carlsen KC, Lindblad A, Dankert-Roelse JE, Ross-Russell RI, Turner SW, Midulla F, Hedlin G. Eber E, et al. Among authors: aurora p. Eur Respir J. 2012 Jul;40(1):215-26. doi: 10.1183/09031936.00226811. Epub 2012 Feb 23. Eur Respir J. 2012. PMID: 22362855 Free article. Review.
Authors' Reply.
Hebestreit H, Arets HG, Aurora P, Boas S, Cerny F, Hulzebos EH, Karila C, Lands LC, Lowman JD, Swisher A, Urquhart DS; Cystic Fibrosis Exercise Working Group. Hebestreit H, et al. Among authors: aurora p. Respiration. 2016;92(1):63-4. doi: 10.1159/000447654. Epub 2016 Jul 1. Respiration. 2016. PMID: 27376551 Free PMC article. No abstract available.
A Simple Screening Test for Cystic Fibrosis?
Davies G, Aurora P. Davies G, et al. Among authors: aurora p. Indian Pediatr. 2019 Feb 15;56(2):105-106. Indian Pediatr. 2019. PMID: 30819986 Free article. No abstract available.
Update on paediatric lung transplantation.
Doherty GM, Aurora P. Doherty GM, et al. Among authors: aurora p. Paediatr Respir Rev. 2010 Mar;11(1):54-61. doi: 10.1016/j.prrv.2009.11.001. Epub 2009 Dec 16. Paediatr Respir Rev. 2010. PMID: 20113993 Review.
Dominant and recessive SLC12A2-syndrome.
McNeill A, Aurora P, Rajput K, Nash R, Stals K, Robinson H, Wakeling E. McNeill A, et al. Among authors: aurora p. Am J Med Genet A. 2022 Mar;188(3):996-999. doi: 10.1002/ajmg.a.62573. Epub 2021 Nov 19. Am J Med Genet A. 2022. PMID: 34797034 No abstract available.
144 results