L. Steinmüller-Magin

Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study

L. Holdt, C. Durmaz, K. Giehl, 2019, The British journal of dermatology.

Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema

U. Jappe, D. Zillikens, G. Gillessen‐kaesbach, 2019, Clinical and Translational Allergy.

Hereditary angioedema with a mutation in the plasminogen gene

I. Braenne, K. Bork, K. Wulff, 2018, Allergy.

Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N‐terminal cleavage site of bradykinin

I. Braenne, H. Rossmann, K. Bork, 2019, Allergy.

Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation.

Britta S. Möhl, K. Bork, K. Wulff, 2021, The Journal of allergy and clinical immunology.

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema

I. Braenne, K. Bork, K. Wulff, 2018, Allergy.

Cardiac transthyretin/leukocyte chemotactic factor (LECT) 2 double amyloidosis in a patient suffering from heart failure

R. Casadonte, K. Klingel, R. Bekeredjian, 2022, Clinical Research in Cardiology.

Prevalence of hereditary transthyretin amyloid polyneuropathy in idiopathic progressive neuropathy in conurban areas

K. Herrmann, T. Rassaf, C. Rischpler, 2019, Neurological Research and Practice.