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

Year Number of Results
1975 1
1976 1
1981 2
1983 2
1984 1
1985 1
1987 1
2006 6
2007 10
2008 23
2009 17
2010 18
2011 18
2012 22
2013 30
2014 20
2015 37
2016 39
2017 33
2018 25
2019 21
2020 49
2021 35
2022 31
2023 23
2024 22

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413 results

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Page 1
Vitamin B12 deficiency - A 21st century perspective .
Shipton MJ, Thachil J. Shipton MJ, et al. Among authors: thachil j. Clin Med (Lond). 2015 Apr;15(2):145-50. doi: 10.7861/clinmedicine.15-2-145. Clin Med (Lond). 2015. PMID: 25824066 Free PMC article. Review.
Iron deficiency without anaemia: a diagnosis that matters.
Al-Naseem A, Sallam A, Choudhury S, Thachil J. Al-Naseem A, et al. Among authors: thachil j. Clin Med (Lond). 2021 Mar;21(2):107-113. doi: 10.7861/clinmed.2020-0582. Clin Med (Lond). 2021. PMID: 33762368 Free PMC article. Review.
Diagnosis and management of sepsis-induced coagulopathy and disseminated intravascular coagulation.
Iba T, Levy JH, Warkentin TE, Thachil J, van der Poll T, Levi M; Scientific and Standardization Committee on DIC, and the Scientific and Standardization Committee on Perioperative and Critical Care of the International Society on Thrombosis and Haemostasis. Iba T, et al. Among authors: thachil j. J Thromb Haemost. 2019 Nov;17(11):1989-1994. doi: 10.1111/jth.14578. Epub 2019 Aug 13. J Thromb Haemost. 2019. PMID: 31410983 Free article. Review. No abstract available.
Disseminated intravascular coagulation in paediatrics.
Rajagopal R, Thachil J, Monagle P. Rajagopal R, et al. Among authors: thachil j. Arch Dis Child. 2017 Feb;102(2):187-193. doi: 10.1136/archdischild-2016-311053. Epub 2016 Aug 18. Arch Dis Child. 2017. PMID: 27540263 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.
413 results