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

Year Number of Results
1984 1
1988 6
1989 3
1990 2
1993 1
1994 1
1995 1
1996 1
1997 5
1999 2
2000 2
2002 2
2004 2
2007 1
2015 1
2016 2
2017 3
2018 2
2019 1
2020 3
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39 results
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Page 1
Hereditary angioedema with a mutation in the plasminogen gene.
Bork K, Wulff K, Steinmüller-Magin L, Braenne I, Staubach-Renz P, Witzke G, Hardt J. Bork K, et al. Allergy. 2018 Feb;73(2):442-450. doi: 10.1111/all.13270. Epub 2017 Sep 7. Allergy. 2018. PMID: 28795768
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema.
Germenis AE, Loules G, Zamanakou M, Psarros F, González-Quevedo T, Speletas M, Bork K, Wulff K, Steinmüller-Magin L, Braenne I, Staubach-Renz P, Witzke G, Hardt J. Germenis AE, et al. Allergy. 2018 Aug;73(8):1751-1753. doi: 10.1111/all.13324. Allergy. 2018. PMID: 30009523 No abstract available.
Molecular biology and clinical manifestation of hereditary factor VII deficiency.
Herrmann FH, Wulff K, Auberger K, Aumann V, Bergmann F, Bergmann K, Bratanoff E, Franke D, Grundeis M, Kreuz W, Lenk H, Losonczy H, Maak B, Marx G, Mauz-Körholz C, Pollmann H, Serban M, Sutor A, Syrbe G, Vogel G, Weinstock N, Wenzel E, Wolf K. Herrmann FH, et al. Semin Thromb Hemost. 2000;26(4):393-400. doi: 10.1055/s-2000-8458. Semin Thromb Hemost. 2000. PMID: 11092214 Review.
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