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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2013 | 1 |
2020 | 1 |
2021 | 2 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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Page 1
Challenges for NHS hospitals during covid-19 epidemic.
BMJ. 2020 Mar 20;368:m1117. doi: 10.1136/bmj.m1117.
BMJ. 2020.
PMID: 32198166
No abstract available.
In utero origin of myelofibrosis presenting in adult monozygotic twins.
Sousos N, Ní Leathlobhair M, Simoglou Karali C, Louka E, Bienz N, Royston D, Clark SA, Hamblin A, Howard K, Mathews V, George B, Roy A, Psaila B, Wedge DC, Mead AJ.
Sousos N, et al. Among authors: bienz n.
Nat Med. 2022 Jun;28(6):1207-1211. doi: 10.1038/s41591-022-01793-4. Epub 2022 May 30.
Nat Med. 2022.
PMID: 35637336
Free PMC article.
Item in Clipboard
Care of haematology patients in an overwhelmed healthcare system.
Willan J, King A, Bienz N, Collins GP.
Willan J, et al. Among authors: bienz n.
Br J Haematol. 2021 Apr;193(2):269-270. doi: 10.1111/bjh.17358. Epub 2021 Feb 17.
Br J Haematol. 2021.
PMID: 33595096
No abstract available.
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Post-COVID-19 syndrome in patients with haematological disorders who have survived infection with severe acute respiratory syndrome coronavirus-2.
Willan J, Hernandez L, Katz H, Gray N, Bienz N.
Willan J, et al. Among authors: bienz n.
Br J Haematol. 2022 Apr;197(2):e19-e23. doi: 10.1111/bjh.18010. Epub 2021 Dec 28.
Br J Haematol. 2022.
PMID: 34961926
No abstract available.
Item in Clipboard
Mortality and burden of post-COVID-19 syndrome have reduced with time across SARS-CoV-2 variants in haematology patients.
Willan J, Agarwal G, Bienz N.
Willan J, et al. Among authors: bienz n.
Br J Haematol. 2023 May;201(4):640-644. doi: 10.1111/bjh.18700. Epub 2023 Mar 2.
Br J Haematol. 2023.
PMID: 36861893
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Impact of isolated germline JAK2V617I mutation on human hematopoiesis.
Mead AJ, Chowdhury O, Pecquet C, Dusa A, Woll P, Atkinson D, Burns A, Score J, Rugless M, Clifford R, Moule S, Bienz N, Vyas P, Cross N, Gale RE, Henderson S, Constantinescu SN, Schuh A, Jacobsen SE.
Mead AJ, et al. Among authors: bienz n.
Blood. 2013 May 16;121(20):4156-65. doi: 10.1182/blood-2012-05-430926. Epub 2013 Mar 27.
Blood. 2013.
PMID: 23535062
Free article.
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Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
Ahmed MR, Chehal A, Zahed L, Taher A, Haidar J, Shamseddine A, O'Hea AM, Bienz N, Dgany O, Avidan N, Beckmann JS, Tamary H, Higgs D, Vyas P, Wood WG, Wickramasinghe SN.
Ahmed MR, et al. Among authors: bienz n.
Blood. 2006 Jun 15;107(12):4968-9. doi: 10.1182/blood-2006-01-0081.
Blood. 2006.
PMID: 16754775
Free article.
No abstract available.
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