Lista de obras -

Alternative complement pathway activation during invasive coronary procedures in acute myocardial infarction and stable angina pectoris

artículo científico publicado en 2016

Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema

artículo científico publicado en 2017

Complement activation in thrombotic thrombocytopenic purpura ⬇️

artículo científico publicado el 1 de mayo de 2012

Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2015

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor

artículo científico publicado en 2020

Elevated plasma neutrophil elastase concentration is associated with disease activity in patients with thrombotic thrombocytopenic purpura

artículo científico publicado en 2014

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

artículo científico publicado en 2015

Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema

artículo científico publicado en 2014

Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients

artículo científico publicado en 2015

Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency

artículo científico publicado en 2017

High anti‐EBNA‐1 IgG levels are associated with early‐onset myasthenia gravis ⬇️

artículo científico publicado el 4 de enero de 2012

Maternal and Fetal Outcomes of Pregnancies in Women with Atypical Hemolytic Uremic Syndrome.

artículo científico publicado en 2017

Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2015

Preemptive plasma therapy prevents atypical hemolytic uremic syndrome relapse in kidney transplant recipients

artículo científico publicado en 2019

Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.

artículo científico publicado en 2016

Sex Differences in Clinical Presentation and Outcomes among Patients with Complement-Gene-Variant-Mediated Thrombotic Microangiopathy

artículo científico publicado en 2020

Short-term prophylaxis in a patient with acquired C1-INH deficiency

artículo científico publicado en 2014

Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor--a long-term survey

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2018

The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2014

The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

artículo científico publicado en 2022

Treatment with C1-inhibitor concentrate does not induce IgM type anti-C1 inhibitor antibodies in patients with hereditary angioedema ⬇️

artículo científico publicado el 15 de diciembre de 2010

Lista de obras de

Alternative complement pathway activation during invasive coronary procedures in acute myocardial infarction and stable angina pectoris

Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema

Complement activation in thrombotic thrombocytopenic purpura ⬇️

Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor

Elevated plasma neutrophil elastase concentration is associated with disease activity in patients with thrombotic thrombocytopenic purpura

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema

Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients

Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency

High anti‐EBNA‐1 IgG levels are associated with early‐onset myasthenia gravis ⬇️

Maternal and Fetal Outcomes of Pregnancies in Women with Atypical Hemolytic Uremic Syndrome.

Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

Preemptive plasma therapy prevents atypical hemolytic uremic syndrome relapse in kidney transplant recipients

Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.

Sex Differences in Clinical Presentation and Outcomes among Patients with Complement-Gene-Variant-Mediated Thrombotic Microangiopathy

Short-term prophylaxis in a patient with acquired C1-INH deficiency

Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor--a long-term survey

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency

The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

Treatment with C1-inhibitor concentrate does not induce IgM type anti-C1 inhibitor antibodies in patients with hereditary angioedema ⬇️