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

Year Number of Results
2008 1
2011 2
2012 1
2014 3
2015 3
2016 7
2017 5
2018 3
2019 8
2020 8
2021 9
2022 5
2023 4
2024 2

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47 results

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Page 1
Inherited platelet disorders in women.
Gresele P, Falcinelli E, Bury L. Gresele P, et al. Among authors: bury l. Thromb Res. 2019 Sep;181 Suppl 1:S54-S59. doi: 10.1016/S0049-3848(19)30368-8. Thromb Res. 2019. PMID: 31477229 Review.
Platelet function assays in diagnosis: an update.
Gresele P, Bury L, Mezzasoma AM, Falcinelli E. Gresele P, et al. Among authors: bury l. Expert Rev Hematol. 2019 Jan;12(1):29-46. doi: 10.1080/17474086.2019.1562333. Epub 2019 Jan 16. Expert Rev Hematol. 2019. PMID: 30571151 Review.
Expanding the genetic spectrum of TUBB1-related thrombocytopenia.
Palma-Barqueros V, Bury L, Kunishima S, Lozano ML, Rodríguez-Alen A, Revilla N, Bohdan N, Padilla J, Fernández-Pérez MP, de la Morena-Barrio ME, Marín-Quilez A, Benito R, López-Fernández MF, Marcellini S, Zamora-Cánovas A, Vicente V, Martínez C, Gresele P, Bastida JM, Rivera J. Palma-Barqueros V, et al. Among authors: bury l. Blood Adv. 2021 Dec 28;5(24):5453-5467. doi: 10.1182/bloodadvances.2020004057. Blood Adv. 2021. PMID: 34516618 Free PMC article.
Search for SARS-CoV-2 RNA in platelets from COVID-19 patients.
Bury L, Camilloni B, Castronari R, Piselli E, Malvestiti M, Borghi M, KuchiBotla H, Falcinelli E, Petito E, Amato F, Paliani U, Vaudo G, Cerotto V, Gori F, Becattini C, De Robertis E, Lazzarini T, Castaldo G, Mencacci A, Gresele P. Bury L, et al. Platelets. 2021 Feb 17;32(2):284-287. doi: 10.1080/09537104.2020.1859104. Epub 2020 Dec 21. Platelets. 2021. PMID: 33349108
Role of endothelial dysfunction in the thrombotic complications of COVID-19 patients.
Falcinelli E, Petito E, Becattini C, De Robertis E, Paliani U, Sebastiano M, Vaudo G, Guglielmini G, Paciullo F, Cerotto V, Malvestiti M, Gori F, Bury L, Lazzarini T, Gresele P; COVIR study investigators. Falcinelli E, et al. Among authors: bury l. J Infect. 2021 May;82(5):186-230. doi: 10.1016/j.jinf.2020.11.041. Epub 2020 Dec 2. J Infect. 2021. PMID: 33275957 Free PMC article. No abstract available.
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes.
Branchini A, Morfini M, Lunghi B, Belvini D, Radossi P, Bury L, Serino ML, Giordano P, Cultrera D, Molinari AC, Napolitano M, Bigagli E, Castaman G, Pinotti M, Bernardi F; GePKHIS Study Group of AICE. Branchini A, et al. Among authors: bury l. J Thromb Haemost. 2022 Jan;20(1):69-81. doi: 10.1111/jth.15552. Epub 2021 Oct 24. J Thromb Haemost. 2022. PMID: 34626083 Free PMC article.
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants.
Bury L, Megy K, Stephens JC, Grassi L, Greene D, Gleadall N, Althaus K, Allsup D, Bariana TK, Bonduel M, Butta NV, Collins P, Curry N, Deevi SVV, Downes K, Duarte D, Elliott K, Falcinelli E, Furie B, Keeling D, Lambert MP, Linger R, Mangles S, Mapeta R, Millar CM, Penkett C, Perry DJ, Stirrups KE, Turro E, Westbury SK, Wu J, BioResource N, Gomez K, Freson K, Ouwehand WH, Gresele P, Simeoni I. Bury L, et al. Hum Mutat. 2020 Jan;41(1):277-290. doi: 10.1002/humu.23927. Epub 2019 Oct 15. Hum Mutat. 2020. PMID: 31562665 Free PMC article.
47 results