Konrad Bork

发表

Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

M. Triggiani, W. Aberer, J. Bernstein, 2014, Allergy.

Hereditary progressive mucinous histiocytosis in women. Report of three members in a family.

K. Bork, N. Hoede, Konrad Bork, 1988, Archives of dermatology.

Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patients with hereditary angioedema.

K. Bork, S. Barnstedt, Konrad Bork, 2001, Archives of internal medicine.

Hereditary angio‐oedema with normal C1 inhibitor in a family with affected women and men

K. Bork, G. Dewald, D. Gül, 2006, The British journal of dermatology.

Asphyxiation by laryngeal edema in patients with hereditary angioedema.

K. Bork, W. Kreuz, R. Schopf, 2000, Mayo Clinic proceedings.

Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations

K. Bork, K. Wulff, J. Hardt, 2015, Allergy.

Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams–Oliver syndrome

K. Bork, J. Jfeifle, Konrad Bork, 1992, The British journal of dermatology.

Increasing incidence of eczema herpeticum: analysis of seventy-five cases.

K. Bork, W. Bräuninger, Konrad Bork, 1988, Journal of the American Academy of Dermatology.

Evidence‐based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: consensus report of an International Working Group

M. Triggiani, W. Aberer, R. Perricone, 2012, Allergy.

Hereditary angioedema with a mutation in the plasminogen gene

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

Treatment of skin swellings with C1‐inhibitor concentrate in patients with hereditary angio‐oedema

K. Bork, P. Staubach, J. Hardt, 2008, Allergy.

Long-term prophylaxis with C1-inhibitor (C1 INH) concentrate in patients with recurrent angioedema caused by hereditary and acquired C1-inhibitor deficiency.

K. Bork, G. Witzke, Konrad Bork, 1989, The Journal of allergy and clinical immunology.

Pruritus precipitated by hydroxyethyl starch: a review

K. Bork, Konrad Bork, 2005, The British journal of dermatology.

Long-standing pigmented keloid of the ears induced by electrical torture.

K. Bork, C. Nagel, Konrad Bork, 1997, Journal of the American Academy of Dermatology.

A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family

E. Donadi, H. Arcuri, E. Castelli, 2011, Allergy.

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.

Primary plasmacytoma of the skin.

T. Tüting, K. Bork, Konrad Bork, 1996, Journal of the American Academy of Dermatology.

Current Status of Implementation of Self-Administration Training in Various Regions of Europe, Canada and the USA in the Management of Hereditary Angioedema

P. Keith, T. Craig, S. Neri, 2013, International Archives of Allergy and Immunology.

Hereditary angioneurotic oedema and blood-coagulation: Interaction between C1-esterase-inhibitor and the activation factors of the proteolytic enzyme systems

K. Bork, P. Beneš, G. Witzke, 1983, Klinische Wochenschrift.