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

Year Number of Results
1990 1
1992 3
1993 2
1998 1
2000 1
2001 4
2002 1
2005 1
2008 1
2009 3
2010 5
2011 4
2012 3
2013 3
2014 3
2015 1
2016 2
2017 3
2018 2
2019 5
2020 3
2021 1
2022 2
2023 1
2024 1

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47 results

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Page 1
Prehospital Lyophilized Plasma Transfusion for Trauma-Induced Coagulopathy in Patients at Risk for Hemorrhagic Shock: A Randomized Clinical Trial.
Jost D, Lemoine S, Lemoine F, Derkenne C, Beaume S, Lanoë V, Maurin O, Louis-Delaurière E, Delacote M, Dang-Minh P, Franchin-Frattini M, Bihannic R, Savary D, Levrat A, Baudouin C, Trichereau J, Salomé M, Frattini B, Ha VHT, Jouffroy R, Seguineau E, Titreville R, Roquet F, Stibbe O, Vivien B, Verret C, Bignand M, Travers S, Martinaud C, Arock M, Raux M, Prunet B, Ausset S, Sailliol A, Tourtier JP; Prehospital Lyophilized Plasma (PREHO-PLYO) Study Group. Jost D, et al. JAMA Netw Open. 2022 Jul 1;5(7):e2223619. doi: 10.1001/jamanetworkopen.2022.23619. JAMA Netw Open. 2022. PMID: 35881397 Free PMC article. Clinical Trial.
Cytogenetic Assessment and Risk Stratification in Myelofibrosis with Optical Genome Mapping.
Díaz-González Á, Mora E, Avetisyan G, Furió S, De la Puerta R, Gil JV, Liquori A, Villamón E, García-Hernández C, Santiago M, García-Ruiz C, Llop M, Ferrer-Lores B, Barragán E, García-Palomares S, Mayordomo E, Luna I, Vicente A, Cordón L, Senent L, Álvarez-Larrán A, Cervera J, De la Rubia J, Hernández-Boluda JC, Such E. Díaz-González Á, et al. Among authors: senent l. Cancers (Basel). 2023 Jun 2;15(11):3039. doi: 10.3390/cancers15113039. Cancers (Basel). 2023. PMID: 37297002 Free PMC article.
Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients.
Ibáñez M, Such E, Liquori A, Avestisyan G, Andreu R, Vicente A, Macián MJ, Melendez MC, Morote-Faubel M, Asensi P, Lloret MP, Jarque I, Picón I, Pacios A, Donato E, Mas-Ochoa C, Alonso C, Cañigral C, Sempere A, Romero S, Santiago M, Sanz GF, de la Rubia J, Senent L, Luna I. Ibáñez M, et al. Among authors: senent l. Diagnostics (Basel). 2022 Apr 11;12(4):953. doi: 10.3390/diagnostics12040953. Diagnostics (Basel). 2022. PMID: 35454001 Free PMC article.
Proposed global prognostic score for systemic mastocytosis: a retrospective prognostic modelling study.
Muñoz-González JI, Álvarez-Twose I, Jara-Acevedo M, Zanotti R, Perkins C, Jawhar M, Sperr WR, Shoumariyeh K, Schwaab J, Greiner G, Henriques A, Caldas C, Fernández-Giménez C, Sánchez-Muñoz L, Mayado A, Pérez-Pons A, Schmitt-Graeff A, Duyster J, Tanasi I, Olivieri F, Mora-Casterá E, Luna I, Senent L, Bañas MH, Nuñez-García A, Jurado-Chacón M, Martín-Sánchez G, Colado E, Xicoy B, Gener-Ricós G, Gotlib J, Bonadonna P, Reiter A, Valent P, García-Montero AC, Orfao A. Muñoz-González JI, et al. Among authors: senent l. Lancet Haematol. 2021 Mar;8(3):e194-e204. doi: 10.1016/S2352-3026(20)30400-2. Epub 2021 Jan 25. Lancet Haematol. 2021. PMID: 33508247
BRAF V600E mutation in adult acute lymphoblastic leukemia.
Alonso CM, Such E, Gómez-Seguí I, Cervera J, Martínez-Cuadrón D, Luna I, Ibáñez M, López-Pavía M, Vera B, Navarro I, Senent L, Sanz Alonso MA. Alonso CM, et al. Among authors: senent l. Leuk Lymphoma. 2013 May;54(5):1105-6. doi: 10.3109/10428194.2012.733878. Epub 2012 Oct 16. Leuk Lymphoma. 2013. PMID: 23009221 No abstract available.
Copper deficiency: a cause of misdiagnosis of myelodysplastic syndrome.
Villalba A, Osorio J, Freiria C, Santiago M, Boluda B, Vicente AI, Sempere A, Andreu R, Gomis F, Senent L. Villalba A, et al. Among authors: senent l. Ann Hematol. 2018 Sep;97(9):1737-1738. doi: 10.1007/s00277-018-3334-5. Epub 2018 Apr 17. Ann Hematol. 2018. PMID: 29663030 No abstract available.
Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.
Bogliolo M, Pujol R, Aza-Carmona M, Muñoz-Subirana N, Rodriguez-Santiago B, Casado JA, Rio P, Bauser C, Reina-Castillón J, Lopez-Sanchez M, Gonzalez-Quereda L, Gallano P, Catalá A, Ruiz-Llobet A, Badell I, Diaz-Heredia C, Hladun R, Senent L, Argiles B, Bergua Burgues JM, Bañez F, Arrizabalaga B, López Almaraz R, Lopez M, Figuera Á, Molinés A, Pérez de Soto I, Hernando I, Muñoz JA, Del Rosario Marin M, Balmaña J, Stjepanovic N, Carrasco E, Cuesta I, Cosuelo JM, Regueiro A, Moraleda Jimenez J, Galera-Miñarro AM, Rosiñol L, Carrió A, Beléndez-Bieler C, Escudero Soto A, Cela E, de la Mata G, Fernández-Delgado R, Garcia-Pardos MC, Sáez-Villaverde R, Barragaño M, Portugal R, Lendinez F, Hernadez I, Vagace JM, Tapia M, Nieto J, Garcia M, Gonzalez M, Vicho C, Galvez E, Valiente A, Antelo ML, Ancliff P, Garcia F, Dopazo J, Sevilla J, Paprotka T, Pérez-Jurado LA, Bueren J, Surralles J. Bogliolo M, et al. Among authors: senent l. J Med Genet. 2020 Apr;57(4):258-268. doi: 10.1136/jmedgenet-2019-106249. Epub 2019 Oct 5. J Med Genet. 2020. PMID: 31586946
47 results