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Results by year

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

Year Number of Results
1973 2
1974 1
1975 1
1976 3
1977 3
1978 1
1979 3
1980 2
1981 2
1982 3
1983 1
1984 2
1985 2
1986 3
1990 4
1991 1
1992 1
1993 1
2002 2
2003 2
2004 1
2007 2
2009 3
2010 3
2011 4
2012 1
2013 1
2014 1
2015 1
2016 4
2017 3
2018 4
2019 2
2020 8
2021 5
2024 0

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PubMed for id: 987194

78 results

Results by year

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Page 1
Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.
Gindele R, Kerényi A, Kállai J, Pfliegler G, Schlammadinger Á, Szegedi I, Major T, Szabó Z, Bagoly Z, Kiss C, Kappelmayer J, Bereczky Z. Gindele R, et al. Life (Basel). 2021 Mar 5;11(3):202. doi: 10.3390/life11030202. Life (Basel). 2021. PMID: 33807613 Free PMC article.
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.
Barco S, Sollfrank S, Trinchero A, Adenaeuer A, Abolghasemi H, Conti L, Häuser F, Kremer Hovinga JA, Lackner KJ, Loewecke F, Miloni E, Vazifeh Shiran N, Tomao L, Wuillemin WA, Zieger B, Lämmle B, Rossmann H. Barco S, et al. J Thromb Haemost. 2020 Jul;18(7):1598-1617. doi: 10.1111/jth.14805. Epub 2020 May 15. J Thromb Haemost. 2020. PMID: 32202057 Free article.
78 results