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Allergy|May 9, 2015
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutationsK Bork, K Wulff, G Witzke, et al.
Ugeskrift for Laeger|April 10, 1995
[Ataxia telangiectasia]L K Hansen, K Wulff, N J Seersholm
Acta Paediatrica (Oslo, Norway : 1992)|February 1, 1993
Early treatment with nasal continuous positive airway pressure in very low-birth-weight infantsJ Kamper, K Wulff, C Larsen, et al.
Clinical Chemistry|July 1, 1987
A monoclonal antibody that specifically inhibits human salivary alpha-amylaseM Gerber, K Naujoks, H Lenz, et al.
Allergy|December 2, 2016
Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII)K Bork, K Wulff, G Witzke, et al.
Acta Chirurgica Scandinavica|January 1, 1977
Preoperative normovolemic hemodilution in total hip arthroplasty. A clinical studyA Ahlberg, A Nillius, B Rosberg, et al.
Archives of Internal Medicine|October 1, 1984
Head trauma in hemophilia. A prospective studyW A Andes, K Wulff, W B Smith
Plos One|March 1, 2021
A 4D continuous representation of myocardial velocity fields from tissue phase mapping magnetic resonance imagingBård A Bendiksen, Gary McGinley, Ivar Sjaastad, et al.
Acta Biochimica Polonica|March 4, 2000
Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX geneK Wulff, K Bykowska, S Lopaciuk, et al.
European Journal of Pediatrics|August 1, 1993
Molybdenum cofactor deficiency in two siblings: diagnostic difficultiesL K Hansen, K Wulff, C Dorche, et al.
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