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

Authors

457

  1. AG
    Anders G. Sjöholm

    Lund University, Sweden

    12 publications · 547 citations

    12

    h-index

  2. CS
    Cordula Stover

    University of Leicester, United Kingdom

    12 publications · 370 citations

    12

    h-index

  3. LP
    Louis Pillemer

    Case Western Reserve University, United States

    12 publications · 1.1K citations

    11

    h-index

  4. EJ
    Ed J. Kuijper

    Leiden University Medical Center, Netherlands

    9 publications · 561 citations

    9

    h-index

  5. CA
    Chester A. Alper

    Harvard University, United States

    8 publications · 694 citations

    8

    h-index

1–5 of 457

Venues

  1. The Journal of Immunology

    JI · 17 publications · 690 citations

    13

    h-index

  2. PubMed

    Repository · 12 publications · 740 citations

    12

    h-index

  3. The Journal of Experimental Medicine

    8 publications · 983 citations

    8

    h-index

  4. Clinical & Experimental Immunology

    CEI · 8 publications · 385 citations

    8

    h-index

  5. New England Journal of Medicine

    NEJM · 6 publications · 568 citations

    6

    h-index

1–5