J. Hardt

K. Bork, A. Bygum, J. Hardt, 2008, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Hereditary Angioedema: Long-Term Treatment with One or More Injections of C1 Inhibitor Concentrate per Week

K. Bork, J. Hardt, 2010, International Archives of Allergy and Immunology.

Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.

K. Bork, K. Wulff, P. Staubach, 2009, The Journal of allergy and clinical immunology.

Symptoms, Course, and Complications of Abdominal Attacks in Hereditary Angioedema Due to C1 Inhibitor Deficiency

A. Eckardt, K. Bork, P. Staubach, 2006, The American Journal of Gastroenterology.

Blindness, tetraspasticity, and other signs of irreversible brain damage in hereditary angioedema.

S. Boor, K. Bork, R. Brehler, 2017, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Kallikrein–kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309Lys

K. Bork, J. Hardt, G. Witzke, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.

K. Bork, J. Hardt, G. Dewald, 2007, The American journal of medicine.

Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence

T. Machnig, K. Bork, K. Wulff, 2020, Orphanet Journal of Rare Diseases.

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.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

Hereditary angioedema: increased number of attacks after frequent treatments with C1 inhibitor concentrate.

K. Bork, J. Hardt, 2009, The American journal of medicine.

Treatment for hereditary angioedema with normal C1‐INH and specific mutations in the F12 gene (HAE‐FXII)

K. Bork, K. Wulff, J. Hardt, 2017, 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.

Angioedema due to acquired C1-inhibitor deficiency: spectrum and treatment with C1-inhibitor concentrate

K. Bork, P. Staubach‐Renz, J. Hardt, 2019, Orphanet Journal of Rare Diseases.

Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene

T. Machnig, K. Bork, K. Wulff, 2020, Orphanet Journal of Rare Diseases.

Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor

K. Bork, K. Wulff, P. Lohse, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations.

K. Bork, K. Wulff, P. Lohse, 2013, The American journal of medicine.

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema

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

Tamoxifen may cause life‐threatening angioedema attacks in patients with hereditary angioedema

K. Bork, K. Wulff, J. Hardt, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Forensic Identification: Dental Scan Data Sets of the Palatal Fold Pairs as an Individual Feature in a Longitudinal Cohort Study

K. Petrowski, D. Thiem, K. Lehmann, 2023, International journal of environmental research and public health.

Forensic Age Estimation: A Multifactorial Approach in a Retrospective Population Study

K. Petrowski, Sebastian Reder, J. Hardt, 2023, Diagnostics.

Psychosocial morbidity of Graves’ orbitopathy

U. Egle, F. Petrak, J. Hardt, 2005, Clinical endocrinology.

Blindness, tetraspasticity, and other signs of irreversible brain damage in hereditary angioedema.

S. Boor, K. Bork, R. Brehler, 2017, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Risk of laryngeal edema and facial swellings after tooth extraction in patients with hereditary angioedema with and without prophylaxis with C1 inhibitor concentrate: a retrospective study.

K. Bork, P. Staubach‐Renz, J. Hardt, 2011, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.

K. Bork, K. Wulff, P. Staubach, 2009, The Journal of allergy and clinical immunology.