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

Year Number of Results
2005 1
2006 1
2007 1
2008 1
2010 1
2011 3
2012 6
2013 5
2014 3
2015 3
2016 3
2017 7
2018 8
2019 8
2020 11
2021 1
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54 results
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Page 1
Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis - a prospective population-based cohort study.
Borghesi A, Trück J, Asgari S, Sancho-Shimizu V, Agyeman PKA, Bellos E, Giannoni E, Stocker M, Posfay-Barbe KM, Heininger U, Bernhard-Stirnemann S, Niederer-Loher A, Kahlert CR, Natalucci G, Relly C, Riedel T, Kuehni CE, Thorball CW, Chaturvedi N, Martinon-Torres F, Kuijpers TW, Coin L, Wright V, Herberg J, Levin M, Aebi C, Berger C, Fellay J, Schlapbach LJ; EUCLIDS consortium and the Swiss Paediatric Sepsis Study. Borghesi A, et al. Among authors: natalucci g. Clin Infect Dis. 2020 Mar 18;71(10):e614-23. doi: 10.1093/cid/ciaa290. Online ahead of print. Clin Infect Dis. 2020. PMID: 32185379 Free PMC article.
Vertical Transmission of Mycoplasma pneumoniae Infection.
Huber BM, Meyer Sauteur PM, Unger WWJ, Hasters P, Eugster MR, Brandt S, Bloemberg GV, Natalucci G, Berger C. Huber BM, et al. Among authors: natalucci g. Neonatology. 2018;114(4):332-336. doi: 10.1159/000490610. Epub 2018 Aug 8. Neonatology. 2018. PMID: 30089291 Free article. Review.
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