Konrad Bork
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(Suggest an Edit or Addition)Konrad Bork's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond (2004) (638)
- Hereditary angioedema: new findings concerning symptoms, affected organs, and course. (2006) (595)
- Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group (2014) (551)
- Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema. (2010) (496)
- 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema (2010) (489)
- Hereditary angioedema with normal C1-inhibitor activity in women (2000) (481)
- ALDEN, an Algorithm for Assessment of Drug Causality in Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis: Comparison With Case–Control Analysis (2010) (479)
- Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. (2006) (350)
- The international WAO/EAACI guideline for the management of hereditary angioedema—The 2017 revision and update (2018) (347)
- Evidence‐based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: consensus report of an International Working Group (2012) (337)
- Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency. (2012) (334)
- Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. (2006) (318)
- Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. (2008) (307)
- Symptoms, Course, and Complications of Abdominal Attacks in Hereditary Angioedema Due to C1 Inhibitor Deficiency (2006) (258)
- WAO Guideline for the Management of Hereditary Angioedema (2012) (249)
- Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency. (2003) (248)
- Asphyxiation by laryngeal edema in patients with hereditary angioedema. (2000) (231)
- Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema. (2004) (211)
- Treatment of acute edema attacks in hereditary angioedema with a bradykinin receptor-2 antagonist (Icatibant). (2007) (209)
- International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency. (2012) (206)
- Hereditary angioedema with a mutation in the plasminogen gene (2018) (198)
- Benefits and risks of danazol in hereditary angioedema: a long-term survey of 118 patients. (2008) (197)
- Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy. (2009) (182)
- Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patients with hereditary angioedema. (2001) (177)
- HAE international home therapy consensus document (2010) (165)
- Disease expression in women with hereditary angioedema. (2008) (160)
- Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel. (2012) (158)
- Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy. (2003) (157)
- Autoantibody-mediated acquired deficiency of C1 inhibitor. (1987) (155)
- Long-term prophylaxis with C1-inhibitor (C1 INH) concentrate in patients with recurrent angioedema caused by hereditary and acquired C1-inhibitor deficiency. (1989) (153)
- Laryngeal edema and death from asphyxiation after tooth extraction in four patients with hereditary angioedema. (2003) (152)
- Prevention of Hereditary Angioedema Attacks with a Subcutaneous C1 Inhibitor (2017) (139)
- International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency (2016) (138)
- Treatment with C1 inhibitor concentrate in abdominal pain attacks of patients with hereditary angioedema (2005) (135)
- Economic costs associated with acute attacks and long-term management of hereditary angioedema. (2010) (131)
- Hepatocellular adenomas in patients taking danazol for here ditary angiooedema (1999) (127)
- Increasing incidence of eczema herpeticum: analysis of seventy-five cases. (1988) (123)
- 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. (2011) (121)
- A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor. (2011) (118)
- Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course. (2007) (117)
- Diagnosis and treatment of hereditary angioedema with normal C1 inhibitor (2010) (111)
- Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N‐terminal cleavage site of bradykinin (2019) (105)
- The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update (2022) (102)
- Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations (2015) (96)
- Pruritus precipitated by hydroxyethyl starch: a review (2005) (95)
- Cutaneous Side Effects of Drugs (1987) (94)
- The International/Canadian Hereditary Angioedema Guideline (2019) (94)
- Canadian hereditary angioedema guideline (2014) (80)
- Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations. (2008) (79)
- Hereditary angio‐oedema with normal C1 inhibitor in a family with affected women and men (2006) (78)
- Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema (2008) (77)
- Hereditary angioedema with normal C1 inhibitor activity including hereditary angioedema with coagulation factor XII gene mutations. (2006) (77)
- Danazol-induced hepatocellular adenoma in patients with hereditary angio-oedema. (2002) (69)
- Treatment of skin swellings with C1‐inhibitor concentrate in patients with hereditary angio‐oedema (2008) (66)
- Treatment for hereditary angioedema with normal C1‐INH and specific mutations in the F12 gene (HAE‐FXII) (2017) (66)
- [WAO Guideline for the Management of Hereditary Angioedema]. (2015) (66)
- Sudden upper airway obstruction in patients with hereditary angioedema. (2003) (61)
- Acquired C1 inhibitor (C1-INH) deficiency type II. Replacement therapy with C1-INH and analysis of patients' C1-INH and anti-C1-INH autoantibodies. (1989) (60)
- Hereditary angioedema with normal C1 inhibitor. (2013) (59)
- Primary plasmacytoma of the skin. (1996) (55)
- Kallikrein–kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309Lys (2009) (52)
- Hereditary Angioedema: Long-Term Treatment with One or More Injections of C1 Inhibitor Concentrate per Week (2010) (52)
- Long‐term efficacy of danazol treatment in hereditary angioedema (2011) (50)
- Diseases of the Oral Mucosa and the Lips (1996) (49)
- Long-Term Outcomes with Subcutaneous C1-Inhibitor Replacement Therapy for Prevention of Hereditary Angioedema Attacks. (2019) (48)
- Pathogenesis of paraneoplastic follicular hyperkeratotic spicules in multiple myeloma. Follicular and epidermal accumulation of IgG dysprotein and cryoglobulin. (1990) (45)
- Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels. (2016) (43)
- Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence (2020) (42)
- Hereditary angioedema: an update on causes, manifestations and treatment. (2019) (41)
- Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation. (2021) (40)
- Hereditary angioedema: increased number of attacks after frequent treatments with C1 inhibitor concentrate. (2009) (40)
- Pasteurized C1 inhibitor concentrate in hereditary angioedema: pharmacology, safety, efficacy and future directions (2008) (39)
- Overview of hereditary angioedema caused by C1-inhibitor deficiency: assessment and clinical management. (2013) (39)
- Treatment with C1-esterase inhibitor concentrate in type I or II hereditary angioedema: a systematic literature review. (2013) (37)
- Pasteurized and nanofiltered, plasma-derived C1 esterase inhibitor concentrate for the treatment of hereditary angioedema. (2014) (36)
- Helicobacter pylori infection as a triggering factor of attacks in patients with hereditary angioedema. (2007) (35)
- Recurrent angioedema and the threat of asphyxiation. (2010) (35)
- Current Status of Implementation of Self-Administration Training in Various Regions of Europe, Canada and the USA in the Management of Hereditary Angioedema (2013) (34)
- Hereditary angioedema: causes, manifestations and treatment. (2006) (32)
- Hereditary progressive mucinous histiocytosis in women. Report of three members in a family. (1988) (32)
- A Decade of Change: Recent Developments in Pharmacotherapy of Hereditary Angioedema (HAE) (2016) (31)
- Angioedema due to acquired C1-inhibitor deficiency: spectrum and treatment with C1-inhibitor concentrate (2019) (30)
- Hereditary angioedema type III, angioedema associated with angiotensin II receptor antagonists, and female sex. (2004) (29)
- Eosinophil granule proteins in serum and urine of patients with helminth infections and atopic dermatitis (2000) (29)
- 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 (2014) (28)
- Helicobacter pylori Infection as a Triggering Factor of Attacks in Patients with Hereditary Angioedema (2007) (26)
- Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams–Oliver syndrome (1992) (25)
- On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema (2018) (25)
- Antibody-mediated inhibition of FXIIa blocks downstream bradykinin generation. (2018) (25)
- Persistent skin ulcers, mutilations, and acro-osteolysis in hereditary sensory and autonomic neuropathy with phospholipid excretion. Report of a family. (1989) (24)
- Guideline: Hereditary angioedema due to C1 inhibitor deficiency (2019) (23)
- A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family (2011) (23)
- Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations. (2013) (22)
- Current Management Options for Hereditary Angioedema (2012) (22)
- Hereditary angioedema associated with subacute cutaneous lupus erythematosus. (1989) (21)
- Hereditary progressive mucinous histiocytosis. Immunohistochemical and ultrastructural studies in an additional family. (1994) (21)
- Hereditary angioedema and normal C1-inhibitor activity in women (2000) (21)
- Panniculitis due to potassium bromide (1998) (20)
- Efficacy and safety of 2% mupirocin ointment in the treatment of primary and secondary skin infections — an open multicentre trial (1989) (20)
- Definition, aims, and implementation of GA2LEN/HAEi Angioedema Centers of Reference and Excellence (2020) (20)
- Hereditary angioedema with normal C1 inhibition (2009) (19)
- An evidence based therapeutic approach to hereditary and acquired angioedema (2014) (19)
- [Contraception and pregnancy in hereditary angioedema]. (2008) (18)
- Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor (2015) (17)
- The Expanding Spectrum of Mutations in Hereditary Angioedema. (2021) (17)
- [Psoriasis and bullous pemphigoid]. (1987) (17)
- Prior pregnancy and melanoma survival. (1986) (17)
- Episodes of severe dyspnea caused by snoring-induced recurrent edema of the soft palate in hereditary angioedema. (2001) (16)
- Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report (2021) (16)
- Physical forces in blister formation. The role of colloid osmotic pressure and of total osmolality in fluid migration into the rising blister. (1978) (15)
- Shortened Activated Partial Thromboplastin Time May Help in Diagnosing Hereditary and Acquired Angioedema (2016) (15)
- Concentration and kinetic studies of intravenous acyclovir in serum and breast milk of a patient with eczema herpeticum. (1995) (15)
- Efficacy of Different Medical Therapies for the Treatment of Acute Laryngeal Attacks of Hereditary Angioedema due to C1-esterase Inhibitor Deficiency. (2016) (15)
- Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene (2020) (15)
- Diagnosis and treatment of hereditary angioedema with normal C 1 inhibitor (2010) (14)
- Allergic contact dermatitis on a violinist's neck from para‐phenylenediamine in a chin rest stain (1993) (14)
- Current and Prospective Targets of Pharmacologic Treatment of Hereditary Angioedema Types 1 and 2 (2021) (14)
- Long‐term safety of icatibant treatment of patients with angioedema in real‐world clinical practice (2017) (14)
- Effects of ethanol and acetaldehyde on phagocytic functions (2004) (13)
- [Familial congenital hypotrichosis with "uncombable hair," retinal pigmentary dystrophy, juvenile cataract and brachymetacarpia: another entity of the ectodermal dysplasia group]. (1987) (13)
- Blindness, tetraspasticity, and other signs of irreversible brain damage in hereditary angioedema. (2017) (13)
- [Hereditary angioedema in the German-speaking region]. (1998) (12)
- Breakthrough attacks in patients with hereditary angioedema receiving long-term prophylaxis are responsive to icatibant: findings from the Icatibant Outcome Survey (2017) (12)
- Interaction between $$C\bar 1$$ -INA, coagulation, fibrinolysis and kinin system in hereditary angioneurotic edema (HANE) and urticaria (2004) (12)
- [Bromoderma tuberosum caused by anticonvulsive treatment with potassium bromide]. (1992) (11)
- [Hereditary angioneurotic edema. Clinical picture, diagnosis, patient management and drug therapy]. (2008) (11)
- Lichen planus: histologic involvement of an epidermoid cyst. (1983) (10)
- Modern topical glucocorticoids and anti-infectives for superinfected atopic eczema: Do prednicarbate and didecyldimethylammoniumchloride form a rational combination? (1994) (10)
- Subcutaneous C1 inhibitor for prevention of attacks of hereditary angioedema: additional outcomes and subgroup analysis of a placebo-controlled randomized study (2019) (10)
- Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene Variants (2020) (10)
- Diseases of the Lips and Mouth (2009) (10)
- Efficacy of C1 esterase inhibitor concentrate in treatment of cutaneous attacks of hereditary angioedema. (2015) (10)
- Fat-storing hamartoma of dermal dendrocytes. Clinical, histologic, and ultrastructural study. (1990) (10)
- [Prurigo and further diagnostically significant skin symptoms in strongyloidosis]. (1988) (9)
- Hereditary angioedema in children and adolescents – A consensus update on therapeutic strategies for German‐speaking countries (2020) (8)
- Proof‐of‐concept study of icatibant (JE 049), a bradykinin B2 receptor antagonist in treatment of hereditary angioedema (2005) (8)
- Abstracts from the 10th C1-inhibitor deficiency workshop (2017) (8)
- [Symptomatic scleroderma caused by bleomycin]. (1983) (8)
- sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor. (2020) (8)
- Long-standing pigmented keloid of the ears induced by electrical torture. (1997) (8)
- Hereditary Angioedema due to C1 Inhibitor Deficiency (2019) (7)
- Human pasteurized C1-inhibitor concentrate for the treatment of hereditary angioedema due to C1-inhibitor deficiency (2011) (7)
- Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency (2019) (7)
- Management of patients with hereditary angioedema in Germany: comparison with other countries in the Icatibant Outcome Survey (2018) (7)
- Increased frequency of multiple primary melanomas in hereditary familial melanoma. (1981) (7)
- Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes (2020) (6)
- [Multiple lymphocytoma at the point of puncture as complication of acupuncture treatment. Traumatic origin of lymphocytoma]. (1983) (6)
- [Tumor-like lupus vulgaris]. (1981) (6)
- Atypical facial porokeratosis of Mibelli (1991) (6)
- [Multiple simultaneous hematomas of the finger and toe nails with subsequent onychomadesis in pemphigus vulgaris]. (1987) (6)
- Stimulation of T cells by autologous mononuclear leukocytes and epidermal cells in psoriasis (2004) (6)
- Transfer of Aciclovir from Plasma to Human Breast Milk (2000) (6)
- Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema (2021) (6)
- [Hypovolemic shock caused by ascites in hereditary angioedema]. (1998) (6)
- [Paraffin granuloma of the penis]. (1986) (5)
- Review of the Long-Term Safety of a Human Pasteurized C1 Inhibitor Concentrate (2012) (5)
- Acute Edema Blisters on a Skin Swelling: An Unusual Manifestation of Hereditary Angioedema. (2016) (5)
- Multifocal disseminated lipoatrophy secondary to intravenous corticosteroid administration in a patient with adrenal insufficiency. (2002) (5)
- [Flea bites caused by Archaeopsylla erinacei, the hedgehog flea]. (1987) (5)
- Hereditary angioneurotic oedema and blood-coagulation: Interaction between C1-esterase-inhibitor and the activation factors of the proteolytic enzyme systems (1983) (5)
- [Contact dermatitis caused by PVP-iodine]. (2008) (5)
- [Localized cutaneous siderosis following intramuscular iron injections]. (1984) (4)
- The European Register of Hereditary Angioedema: Experience and Preliminary Results (2007) (4)
- [Ascites and suspected acute abdomen in hereditary angioedema due to C1 inhibitor deficiency]. (1997) (4)
- [Pseudoxanthoma elasticum in pregnancy: effects on mother and child]. (1983) (4)
- Metastases of malignant melanoma due to interferon alpha-2a? (1988) (4)
- 25 years of safety experience with C1 inhibitor concentrate in treatment of acute hereditary angioedema attacks (2011) (4)
- Acquired and hereditary forms of recurrent angioedema: Update of treatment (2018) (4)
- [Disseminated lichenoid form of lupus vulgaris]. (1985) (4)
- [Umbilical metastasis of a gallbladder carcinoma: "Sister Mary Joseph's nodule"]. (2002) (4)
- [Stigmas, symptoms and diseases of the skin in musicians]. (1993) (4)
- Tamoxifen may cause life‐threatening angioedema attacks in patients with hereditary angioedema (2017) (4)
- A germline mutation in the platelet‐derived growth factor receptor beta gene may be implicated in hereditary progressive mucinous histiocytosis (2021) (4)
- [Angioedema caused by C1-esterase inhibitor deficiency or ACE inhibitors?]. (2007) (4)
- [Massive upper gastrointestinal bleeding as first clinical manifestation of pseudoxanthoma elasticum (author's transl)]. (1980) (3)
- [Furuncular myiasis caused by Dermatobia hominis larva]. (1981) (3)
- Current drugs in early development for hereditary angioedema: potential for effective treatment (2014) (3)
- [Artificial penile nodules (tancho nodules) in Southeast Asian men]. (1985) (3)
- Side Effects Of Long-Term Treatment With Danazol And Stanozolol In Hereditary Angioedema (2007) (3)
- [Simulation of malignant tumors by undeclared polyvinylpyrrolidone in drugs]. (1982) (3)
- Germline mutation in PDGFRB may be implicated in hereditary progressive mucinous histiocytosis. (2020) (3)
- Cutaneous Adverse Drug Reactions (2009) (3)
- [Pseudotumors and other drug reactions caused by not declared additional substances]. (2008) (3)
- [Extrapalmoplantar skin symptoms and additional clinical, etiological and immunological aspects in particular, in Papillon-Lefevre syndrome]. (1980) (3)
- [Defective polymorphonuclear leukocyte function in chronic granulomatous muco-cutaneous candidiasis (author's transl)]. (1975) (3)
- [Achalasia in circumscribed scleroderma]. (2006) (2)
- [Paget's disease of the vulva and breast carcinoma]. (1976) (2)
- Effectiveness of icatibant for treatment of hereditary angioedema attacks is not affected by body weight: findings from the Icatibant Outcome Survey, a cohort observational study (2018) (2)
- Frenum reduction as a treatment for periodontal atrophy. (1958) (2)
- Uncommon Signs Associated with Hereditary Angioedema with Normal C1 Inhibitor. (2020) (2)
- Hereditary Angioedema with Normal C1-INH with Versus without a Specific Mutation in the F12 Gene (2015) (2)
- Correction to: The International/Canadian Hereditary Angioedema Guideline (2020) (2)
- A review of hereditary angioedema and recombinant human C1-inhibitor treatment (2011) (2)
- Hereditary angioedema: Educational review (2006) (2)
- [Contraceptives and pregnancy in melanoma patients]. (1985) (2)
- Pathogenesis of Hereditary Angioedema with Normal C1 Inhibitor: Evidence for Abnormalities in Plasminogen Activator Inhibitors (2015) (2)
- [Hereditary angioneurotic edema. Clinical aspects and extended diagnostic and therapeutic possibilities]. (1979) (2)
- European Consensus for Gynecologycal and Obstetric Management of Women with Hereditary Angioedema due to C1-Inhibitor Deficiency (HAE): PREHAEAT (2007) (2)
- Genetic Analysis as a Practical Tool for Diagnosis of Hereditary Angioedema With Normal C1 Inhibitor: A Case Report. (2016) (2)
- Diagnosis and treatment of common skin diseases (1990) (2)
- [Hemorrhagic skin necrosis in intravascular precipitation of cryoglobulin by lymphocytic malignant lymphoma]. (1981) (2)
- [Differential diagnosis and therapy of recurrent aphthae]. (1987) (2)
- [Physical bases of blister formation. II. A study of the total osmotic pressure in the blister fluid of suction blisters and of "naturally" occurring blisters as well as in the serum]. (1978) (2)
- [Undifferentiated cutaneous angiosarcoma of the head: identification by the endothelial marker Ulex europaeus agglutinin I]. (1985) (2)
- Hereditary Angioedema Due to C1 Inhibitor Deficiency: New Findings Concerning Symptoms and Affected Organs (2006) (2)
- Mutations in the Factor XII Gene in Solitary Cases of Recurrent Angioedema with Normal C1 Inhibitor Induced or Worsened by Oral Contraceptives or Hormonal Replacement Therapy (2012) (1)
- [Overall progeroid aspect of the Louis-Bar syndrome: pigmentary and keratotic phenomena]. (1979) (1)
- Treatment With Pasteurized C1 Inhibitor Concentrate In Skin Swelling Attacks Of Patients With Hereditary Angioedema (2007) (1)
- [Physical forces in blister formation. I. Direct measurement of blister fluid colloid osmotic pressure in suction blisters and in bullous diseases (author's transl)]. (1977) (1)
- New Mutations of C1 inhibitor (SERPING1/C1NH) Gene Associated with Hereditary Angioedema in a European Population (2007) (1)
- [Multiple skin plasmocytomas, increased serum IgA and lack of bone marrow lesions (author's transl)]. (1975) (1)
- [Skin changes in malignant diseases]. (1983) (1)
- Stimulation of T lymphocytes by isolated autologous or allogeneic human epidermal cells (1984) (1)
- [The chemotactic effect of blister roof, blister fluid and blister floor on polymorphonuclear leucocytes in dermatitis herpetiformis Duhring (author's transl)]. (1975) (1)
- Successful Extubation With Use of C1 Esterase Inhibitor Concentrate in a Patient With Hereditary Angioedema: In Response (2000) (1)
- A systematic review of the efficacy and safety of a purified, pasteurized C1 inhibitor concentrate for the treatment of patients with type I or II hereditary angioedema (2010) (1)
- [Paraneoplastic multicentric reticulohistiocytosis: induced and inductable by iodine containing x-ray contrast media]. (1985) (1)
- [Quantitative measurements of peripheral circulation and further angiologic aspects in patients with elastic pseudoxanthoma]. (1973) (1)
- Icatibant, a Selective Bradykinin-B2 Receptor Antagonist, in Acquired Angioedema Due to C1 Inhibitor Deficiency (2011) (1)
- New drug targets and future direction: icatibant (2012) (1)
- [Ultrastructure of nuclear bodies in connective tissue cells of psoriatic lesions (author's transl)]. (1975) (1)
- 83 Hereditary Angioedema and Normal C1-Inhibitor (HAE TYPE III): A Novel Mutation in the Coagulation Factor 12 Gene (2012) (1)
- [Dermatological aspects of Hildegard von Bingen's work]. (1980) (1)
- Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series (2022) (1)
- Efficacy of C1-Inhibitor Concentrate (Berinert®) for the Treatment of Cutaneous Attacks of Acute Hereditary Angioedema Compared to Historical Untreated Controls (2013) (1)
- [Does a circumscribed melanosis secondary to malignant melanoma exist?]. (1977) (1)
- [Increase of certain serum enzyme levels (GOT, LDH, CPK, MK) after body massage and its significance in dermatomyositis]. (1972) (1)
- [Endocrine influences on malignant melanoma. Survival time of melanoma patients depending on the number of prior pregnancies and menopause begin]. (1981) (1)
- [Dermatoses resulting from contact with plants]. (1981) (1)
- Safety Evaluation of Icatibant, a Selective Bradykinin B2 Receptor Antagonist Used in Hereditary Angioedema Due to C1 Inhibitor Deficiency (2009) (1)
- Analysis of cold activation of the contact system in hereditary angioedema with normal C1 inhibitor. (2021) (1)
- [Phagocytic function of polymorphonuclear leucocytes in psoriatic inflammation (author's transl)]. (1974) (1)
- [Recurring cheilitis, stomatitis and glossitis in Felty's syndrome]. (1976) (1)
- [Physical forces in blister formation. II. Examination of total osmolality in blister fluid of suction blisters, "naturally" developed blisters and in serum (author's transl)]. (1978) (1)
- [Naeviform porokeratosis - only a morphologic variant of porokeratosis of Mibelli (author's transl)]. (1982) (0)
- C1-Esterase Inhibitor Concentrate for Acute Laryngeal Hereditary Angioedema (HAE) Attacks: Different Treatment Response Based on Dosing Regimen? (2016) (0)
- Mutation Analysis in Hereditary Angioedema Identifies Patients at Risk for Developing Acute and Life Threatening Edema (2006) (0)
- Genetic Analysis As a Practical Tool to Diagnose Hereditary Angioedema with Normal C1 Inhibitor: A Case Report (2015) (0)
- Tamoxifen, a Trigger Factor of Hereditary Angioedema with Normal C1-INH with a Specific Mutation in the F12 Gene (HAE-FXII) (2016) (0)
- [Action of some serum enzymes following whole-body muscle massage. Contribution to the problem of physical therapy in dermatomyositis]. (1971) (0)
- [Life threatening laryngeal edema after minor dental treatments in hereditary angioneurotic edema]. (1979) (0)
- Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin (2023) (0)
- Acquired C 1 Inhibitor ( Cl-INH ) Deficiency Type 11 Replacement Therapy with C 1-INH and Analysis of Patients ' C 1-INH and Anti-Cl-INH Autoantibodies (2013) (0)
- [Allergy to denture materials]. (1988) (0)
- [Case report of Papillon-Lefèvre syndrome]. (1980) (0)
- Icatibant, a Selective Bradykinin B2 Receptor Antagonist Used in Hereditary Angioedema Due to C1 Inhibitor Deficiency (2010) (0)
- [Pruritus and bile acids. Determination of sulfalithoglycocholate and glycocholate in suction blister fluid and in serum (author's transl)]. (1981) (0)
- Coagulation factor XII (Hageman factor): a new angioedema gene (2007) (0)
- Novel SERPING1 mutation causing Hereditary Angioedema in a Brazilian family (2009) (0)
- Treatment of skin swellings with pasteurized C1 inhibitor concentrate in patients with hereditary angioedema (2007) (0)
- Contents Vol. 121, 2008 (2008) (0)
- Missense Mutations in the Proline-Rich Region of Coagulation Factor XII in Hereditary and Idiopathic Angioedema. (2006) (0)
- 165 Early Versus Delayed Treatment of Swelling Attacks with Icatibant, a Bradykinin 2 Receptor Antagonist in Patients With Hereditary Angioedema due to C1-INH Deficiency (2012) (0)
- Gene mutations linked with hereditary angioedema in solitary angioedema patients with normal C1-INH. (2023) (0)
- [Side effects of drugs on the skin]. (1992) (0)
- Missense mutations of coagulation factor XII in hereditary angioedema with normal complement C1 inhibitor (2007) (0)
- [Ophthalmoblennorrhea in urethral gonorrhea and consecutive iritis as well as arthropathy despite massive penicillin treatment (postgonnorheic Reiter's syndrome)]. (1972) (0)
- [Formation of IgG antibodies to C1 inhibitor as the cause of life-threatening angioedema]. (1987) (0)
- Impaired function of numerically augmented Fc-receptors on granulocytes in a HLA B8+ patient with palmoplantar pustulosis (2004) (0)
- Currently available treatments and future treatment options for hereditary angioedema (2015) (0)
- Differentialdiagnose und Operationsindikation aus dermatologischer Sicht (1991) (0)
- [Reiter's syndrome following gonorrhea. Urethral gonorrhea and gonoglennorrhea with iridocyclitis and arthritis]. (1972) (0)
- [Concurrence of lichen planus pemphigoides and ulcerative colitis (author's transl)]. (1981) (0)
- [Epithelioma calcificans and injury?]. (1974) (0)
- Der Internist (2019) (0)
- Psoriasis arthropathica und Amyloidose (2004) (0)
- Definitive Link of Mutation c.351delC and Development of Hereditary Angioedema in a Large Brazilian Family (2011) (0)
- Clinical symptoms and treatment in hereditary angioedema with normal C1 inhibitor (2007) (0)
- PSY6 THE ICATIBANT OUTCOME SURVEY:A PROSPECTIVE STUDY OF SAFETY AND EFFECTIVENESS OF ICATIBANT IN A ‘REAL WORLD' SETTING IN PATIENTS WITH HEREDITARY ANGIOEDEMA (2010) (0)
- Angioedema with Negative Family History (2014) (0)
- [Recurrent angioedema (Quincke's edema)-a constant problem]. (1986) (0)
- [Post-meningoencephalitic benign acanthosis nigricans]. (1980) (0)
- [Histamine levels in interstitial fluid of lesional and perilesional skin in patients with chronic idiopathic urticaria (author's transl)]. (1979) (0)
- Hereditary Angioedema: a New Mutation of the C1 Inhibitor Gene in a Brazilian Family (2008) (0)
- [Regional intra-arterial chemotherapy with Dacarbazine in isolated liver metastases of a malignant melanoma]. (2008) (0)
- [Dermatoses in pregnancy]. (1990) (0)
- [Unusual early changes in malignant lymphoma of the B-cell type with a low degree of malignity]. (1980) (0)
- [Pathology of skin and jejunum in dermatitis herpetiformis]. (1978) (0)
- Treatment of Hereditary Angioedema with the Mutation c.988A>G (p.K330E) in the Plasminogen Gene (2020) (0)
- Severe Tongue Swellings In Hereditary Angioedema With A Specific Mutation In The Plasminogen Gene (2018) (0)
- [Psoriasis arthropathica and amyloidosis]. (1972) (0)
- Hereditary Angioedema with Normal C1-Inhibitor: Pathophysiology and Treatment (2017) (0)
- [Allergic rhinitis from metal parts of dental prostheses]. (1978) (0)
- [Skin manifestations in cryoglobulinemia]. (1979) (0)
- Contributions EFFICACY OF DIFFERENT MEDICAL THERAPIES FOR THE TREATMENT OF ACUTE LARYNGEAL ATTACKS OF HEREDITARY ANGIOEDEMA DUE TO C 1-ESTERASE INHIBITOR DEFICIENCY (0)
- The reply. (2014) (0)
- 453 A 26-Year Review of Long-term Safety of a Human Pasteurized C1 Inhibitor Concentrate (2012) (0)
- [The histamine-release test, a new in-vitro method in the diagnosis of allergic diseases (author's transl)]. (1981) (0)
- [Skin testing in allergy to denture plastics]. (1982) (0)
- [Lyell's syndrome with transient bone marrow depression caused by oxyphenebutazone]. (1979) (0)
- LCNG-TEFM SUBSTITUTION WITH Cl-INACTIVATOR IN PATIENTS WITH HEREDITARY AND ACQUIRED Cl-INH DEFICIENCY AND LIFE-THREATENING ANGIOEDEMA (1987) (0)
- Mutation Analysis of the C1 Inhibitor Gene (2005) (0)
- [Quantitative measurement of peripheral circulation and additional new angiologic aspects in patients with Pseudoxanthoma elasticum (author's transl)]. (1974) (0)
- [Cutaneous leishmaniasis in an unusual location and local recurrence]. (1980) (0)
- C1-Esterase Inhibitor Concentrate For Acute Attacks Of Laryngeal Edema In Hereditary Angioedema (HAE): Fixed Dosing Vs Body Weight-Adjusted Dosing (2014) (0)
- [Alexander Tschirch and the interpretation of pharmacognosy]. (2001) (0)
- Author response for "Hereditary angioedema in children and adolescents – A consensus update on therapeutic strategies for German‐speaking countries" (2020) (0)
- [Malignant melanoma in childhool]. (1977) (0)
- [Mercury absorption out of ammoniated mercury ointment (author's transl)]. (1973) (0)
- [What is the best prevention and therapy of bee, wasp and hornet stings?]. (1983) (0)
- Acquired and Hereditary Angioedema: Pathogenesis and Therapy (1988) (0)
- Prophylaxis with C1 Inhibitor Concentrate before Tooth Extractions in Patients with Hereditary Angioedema (2011) (0)
- [Primary melanomatosis]. (1976) (0)
- [Cardiac involvement in urticaria]. (1980) (0)
- [Pregnancy after malignant melanoma. A follow-up of 23 patients]. (1985) (0)
- Inheritance pattern of hereditary angioedema indicates mutation-dependent selective effects during early embryonic development. (2021) (0)
- High exhaled nitric oxide levels correlate with nonadherence in acute asthmatic children (2017) (0)
- Contents, Vol. 179, 1989 (1989) (0)
- Currently available treatments and future treatment options for hereditary angioedema (2015) (0)
- Treatment with Pasteurized C1 Inhibitor Concentrate in Abdominal Pain Attacks of Patients with Hereditary Angioedema (2006) (0)
- Contents, Vol. 166, 1983 (1983) (0)
- Angioedema Due To Acquired C1‐Inhibitor Deficiency: Spectrum And Treatment With C1‐Inhibitor Concentrate: 126 (2019) (0)
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