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

Year Number of Results
1975 1
1979 2
1984 1
1988 3
1989 2
1991 3
1992 1
1993 2
1994 1
1995 4
1996 1
1997 3
1998 2
1999 3
2000 6
2001 2
2002 2
2003 9
2004 10
2005 5
2006 9
2007 6
2008 7
2009 9
2010 7
2011 10
2012 16
2013 11
2014 9
2015 12
2016 12
2017 9
2018 10
2019 11
2020 11
2021 5
2022 3
2023 1
2024 2

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196 results

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Page 1
Immune Thrombocytopenia Treatment.
Bolton-Maggs PHB, George JN. Bolton-Maggs PHB, et al. N Engl J Med. 2021 Sep 2;385(10):948-950. doi: 10.1056/NEJMe2110953. N Engl J Med. 2021. PMID: 34469652 No abstract available.
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
Bolton-Maggs PH, Langer JC, Iolascon A, Tittensor P, King MJ; General Haematology Task Force of the British Committee for Standards in Haematology. Bolton-Maggs PH, et al. Br J Haematol. 2012 Jan;156(1):37-49. doi: 10.1111/j.1365-2141.2011.08921.x. Epub 2011 Nov 5. Br J Haematol. 2012. PMID: 22055020 Free article.
Haemophilias A and B.
Bolton-Maggs PH, Pasi KJ. Bolton-Maggs PH, et al. Lancet. 2003 May 24;361(9371):1801-9. doi: 10.1016/S0140-6736(03)13405-8. Lancet. 2003. PMID: 12781551 Review.
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Carss KJ, Arno G, Erwood M, Stephens J, Sanchis-Juan A, Hull S, Megy K, Grozeva D, Dewhurst E, Malka S, Plagnol V, Penkett C, Stirrups K, Rizzo R, Wright G, Josifova D, Bitner-Glindzicz M, Scott RH, Clement E, Allen L, Armstrong R, Brady AF, Carmichael J, Chitre M, Henderson RHH, Hurst J, MacLaren RE, Murphy E, Paterson J, Rosser E, Thompson DA, Wakeling E, Ouwehand WH, Michaelides M, Moore AT; NIHR-BioResource Rare Diseases Consortium; Webster AR, Raymond FL. Carss KJ, et al. Am J Hum Genet. 2017 Jan 5;100(1):75-90. doi: 10.1016/j.ajhg.2016.12.003. Epub 2016 Dec 29. Am J Hum Genet. 2017. PMID: 28041643 Free PMC article.
International consensus report on the investigation and management of primary immune thrombocytopenia.
Provan D, Stasi R, Newland AC, Blanchette VS, Bolton-Maggs P, Bussel JB, Chong BH, Cines DB, Gernsheimer TB, Godeau B, Grainger J, Greer I, Hunt BJ, Imbach PA, Lyons G, McMillan R, Rodeghiero F, Sanz MA, Tarantino M, Watson S, Young J, Kuter DJ. Provan D, et al. Among authors: bolton maggs p. Blood. 2010 Jan 14;115(2):168-86. doi: 10.1182/blood-2009-06-225565. Epub 2009 Oct 21. Blood. 2010. PMID: 19846889 Free article. Review.
Guidelines on transfusion for fetuses, neonates and older children.
New HV, Berryman J, Bolton-Maggs PH, Cantwell C, Chalmers EA, Davies T, Gottstein R, Kelleher A, Kumar S, Morley SL, Stanworth SJ; British Committee for Standards in Haematology. New HV, et al. Among authors: bolton maggs ph. Br J Haematol. 2016 Dec;175(5):784-828. doi: 10.1111/bjh.14233. Epub 2016 Nov 11. Br J Haematol. 2016. PMID: 27861734 Free article. No abstract available.
A consensus redefinition of transfusion-related acute lung injury.
Vlaar APJ, Toy P, Fung M, Looney MR, Juffermans NP, Bux J, Bolton-Maggs P, Peters AL, Silliman CC, Kor DJ, Kleinman S. Vlaar APJ, et al. Among authors: bolton maggs p. Transfusion. 2019 Jul;59(7):2465-2476. doi: 10.1111/trf.15311. Epub 2019 Apr 16. Transfusion. 2019. PMID: 30993745 Free PMC article.
Rare bleeding disorders.
Peyvandi F, Bolton-Maggs PH, Batorova A, De Moerloose P. Peyvandi F, et al. Among authors: bolton maggs ph. Haemophilia. 2012 Jul;18 Suppl 4:148-53. doi: 10.1111/j.1365-2516.2012.02841.x. Haemophilia. 2012. PMID: 22726099 Review.
Transfusion errors - can they be eliminated?
Bolton-Maggs PHB, Watt A. Bolton-Maggs PHB, et al. Br J Haematol. 2020 Apr;189(1):9-20. doi: 10.1111/bjh.16256. Epub 2019 Dec 2. Br J Haematol. 2020. PMID: 31792932 Free article.
Factor XI deficiency.
Gomez K, Bolton-Maggs P. Gomez K, et al. Among authors: bolton maggs p. Haemophilia. 2008 Nov;14(6):1183-9. doi: 10.1111/j.1365-2516.2008.01667.x. Epub 2008 Feb 27. Haemophilia. 2008. PMID: 18312365 Review.
196 results