Properdin Deficiency
Properdin Deficiency is a rare X-linked primary immunodeficiency disorder characterized by the impaired stabilization of the alternative pathway C3 convertase due to deficient or dysfunctional properdin, leading to increased susceptibility to recurrent pyogenic infections, particularly Neisseria species.
136
Publications
7.4K
Citations
457
Authors
190
Institutions
Publications per year
2017–2026
9
Parents
136
THE PROPERDIN SYSTEM AND IMMUNITY
Louis Pillemer, Livia Blum, Irwin H. Lepow et al. · The Journal of Experimental Medicine · 1956 · 357 citations · Full text
QUANTITATIVE STUDIES OF PHAGOCYTOSIS
Thomas P. Stossel · The Journal of Cell Biology · 1973 · 208 citations · Full text
THE PROPERDIN SYSTEM AND IMMUNITY
A. C. Wardlaw, Louis Pillemer · The Journal of Experimental Medicine · 1956 · 171 citations · Full text
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190

Lund University
Lund, Sweden
13 h-index
44 publications
1.6K citations

University of Leicester
Leicester, United Kingdom
12 h-index
48 publications
1.2K citations
Case Western Reserve University
Cleveland, United States
11 h-index
41 publications
4.2K citations

University of Amsterdam
Amsterdam, The Netherlands
8 h-index
32 publications
2.8K citations
University of Pennsylvania
Philadelphia, United States
7 h-index
25 publications
1.5K citations
Harvard University
Cambridge, United States
5 h-index
13 publications
1.1K citations
Translational Therapeutics (United States)
Arlington, United States
5 h-index
22 publications
832 citations
Dana-Farber/Boston Children's Cancer and Blood Disorders Center
Boston, United States
4 h-index
14 publications
932 citations
1–8 of 190
JI · 17 publications · 690 citations
13
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Repository · 12 publications · 740 citations
12
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8 publications · 983 citations
8
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CEI · 8 publications · 385 citations
8
h-index
NEJM · 6 publications · 568 citations
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