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Open‐label, multicenter study of self‐administered icatibant for attacks of hereditary angioedema

Allergy (Copenhagen), 2014-03, Vol.69 (3), p.305-314

2014

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Icatibant, a New Bradykinin-Receptor Antagonist, in Hereditary Angioedema

The New England journal of medicine, 2010-08, Vol.363 (6), p.532-541

2010

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Repeat treatment of acute hereditary angioedema attacks with open‐label icatibant in the FAST‐1 trial

Clinical and experimental immunology, 2014-08, Vol.177 (2), p.544-553

2014

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Successful Treatment of 103 Attacks of Hereditary Hngioedema (HAE) with Bradykinin B2 Receptor Antagonist Icatibant

Journal of allergy and clinical immunology, 2008-02, Vol.121 (2), p.S102-S102

Malbran, A

2008

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Rupatadine in the treatment of chronic idiopathic urticaria: a double-blind, randomized, placebo-controlled multicentre study

Allergy, 2007-05, Vol.62 (5), p.539-546

2007

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Efficacy of Icatibant for Cutaneous and Abdominal Attacks of Type I and II Hereditary Angioedema: A Pooled Analysis of Three Phase III trials

Journal of allergy and clinical immunology, 2012-02, Vol.129 (2), p.AB218-AB218

2012

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Diclofenac induces basophil degranulation without increasing CD63 expression in sensitive patients

Clinical and experimental immunology, 2007-01, Vol.147 (1), p.99-105

2007

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

Allergy, 2014-05, Vol.69 (5), p.602-616

2014

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

Allergy, 2012-02, Vol.67 (2), p.147-157

2012

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Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE)

Orphanet journal of rare diseases, 2022-03, Vol.17 (1), p.88-88, Article 88

2022

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Loss of circulating CD27+ memory B cells and CCR4+ T cells occurring in association with elevated EBV loads in XLP patients surviving primary EBV infection

Blood, 2004-03, Vol.103 (5), p.1625-1631

2004

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Diethyltoluamide (DEET) increases CD63 expression in a contact urticaria patient’s basophils

Allergologia et immunopathologia, 2011-01, Vol.39 (1), p.55-57

2011

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Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema

Clinical reviews in allergy & immunology, 2021-08, Vol.61 (1), p.84-97

2021

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Factors involved in the generation of memory CD8⁺ T cells in patients with X-linked lymphoproliferative disease (XLP)

Clinical and experimental immunology, 2007-03, Vol.147 (3), p.456-464

2007

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Diclofenac does not induce basophil CD63 expression in resting basophils from sensitive patients

Journal of allergy and clinical immunology, 2005-02, Vol.115 (2), p.S183-S183

2005

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Vaccination with EG95 against ovine cystic echinococcosis in the province of Río Negro: analysis of 12 years of work

Ciencia Veterinaria, 2022-05, Vol.24 (2), p.241-254

2022

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Acute edema blisters in a hereditary angioedema cutaneous attack

Allergologia et immunopathologia, 2008-05, Vol.36 (3), p.182-183

2008

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12-week placebo-controlled study of rupatadine 10 mg once daily compared with cetirizine 10 mg once daily, in the treatment of persistent allergic rhinitis

Allergy (Copenhagen), 2008-07, Vol.63 (7), p.924-931

2008

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Defects in CD27+ memory B cells and CCR4+ T cells occurring in association with elevated serum Epstein-Barr virus (EBV) loads in XLP patients surviving primary EBV infection1

Journal of allergy and clinical immunology, 2004-02, Vol.113 (2), p.S40-S41

MALBRAN, A

2004

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Treatment of primary Epstein-Barr virus infection in patients with X-linked lymphoproliferative disease using B-cell–directed therapy

Blood, 2005-02, Vol.105 (3), p.994-996

2005

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Defects in CD27+ memory B cells and CCR4+ T cells occurring in association with elevated serum Epstein-Barr virus (EBV) loads in XLP patients surviving primary EBV infection

Journal of allergy and clinical immunology, 2004-02, Vol.113 (2), p.S40-S41

2004

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Ocular Cicatricial Pemphigoid (OCP) Systemic Treatment

Journal of allergy and clinical immunology, 2010-02, Vol.125 (2), p.AB39-AB39

2010

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Poor and minority asthma in Argentina: A descriptive and intervention study

Journal of allergy and clinical immunology, 2005-02, Vol.115 (2), p.S131-S131

2005

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Acquired angioedema: Observations on the mechanism of action of autoantibodies directed against C1 esterase inhibitor

Journal of allergy and clinical immunology, 1988, Vol.81 (6), p.1199-1204

1988

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Open‐label, multicenter study of self‐administered icatibant for attacks of hereditary angioedema

Icatibant, a New Bradykinin-Receptor Antagonist, in Hereditary Angioedema

Repeat treatment of acute hereditary angioedema attacks with open‐label icatibant in the FAST‐1 trial

Successful Treatment of 103 Attacks of Hereditary Hngioedema (HAE) with Bradykinin B2 Receptor Antagonist Icatibant

Rupatadine in the treatment of chronic idiopathic urticaria: a double-blind, randomized, placebo-controlled multicentre study

Efficacy of Icatibant for Cutaneous and Abdominal Attacks of Type I and II Hereditary Angioedema: A Pooled Analysis of Three Phase III trials

Baseline prevalence and type distribution of Human papillomavirus in sexually active non-vaccinated adolescent girls from Argentina

Diclofenac induces basophil degranulation without increasing CD63 expression in sensitive patients

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

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

Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE)

Loss of circulating CD27+ memory B cells and CCR4+ T cells occurring in association with elevated EBV loads in XLP patients surviving primary EBV infection

Diethyltoluamide (DEET) increases CD63 expression in a contact urticaria patient’s basophils

Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema

Factors involved in the generation of memory CD8⁺ T cells in patients with X-linked lymphoproliferative disease (XLP)

Diclofenac does not induce basophil CD63 expression in resting basophils from sensitive patients

Vaccination with EG95 against ovine cystic echinococcosis in the province of Río Negro: analysis of 12 years of work

Acute edema blisters in a hereditary angioedema cutaneous attack

12-week placebo-controlled study of rupatadine 10 mg once daily compared with cetirizine 10 mg once daily, in the treatment of persistent allergic rhinitis

Defects in CD27+ memory B cells and CCR4+ T cells occurring in association with elevated serum Epstein-Barr virus (EBV) loads in XLP patients surviving primary EBV infection1

Treatment of primary Epstein-Barr virus infection in patients with X-linked lymphoproliferative disease using B-cell–directed therapy

Defects in CD27+ memory B cells and CCR4+ T cells occurring in association with elevated serum Epstein-Barr virus (EBV) loads in XLP patients surviving primary EBV infection

Ocular Cicatricial Pemphigoid (OCP) Systemic Treatment

Poor and minority asthma in Argentina: A descriptive and intervention study

Acquired angioedema: Observations on the mechanism of action of autoantibodies directed against C1 esterase inhibitor

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