0000000000347445

AUTHOR

Luisa Karla De Paula Arruda

showing 6 related works from this author

Hereditary Angioedema: a New Mutation of the C1 Inhibitor Gene in a Brazilian Family

2008

Geneticsbiologybusiness.industryImmunologyNew mutationHereditary angioedemabiology.proteinImmunology and AllergyMedicinebusinessmedicine.diseaseGeneC1-inhibitorJournal of Allergy and Clinical Immunology
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Genetic Analysis As a Practical Tool to Diagnose Hereditary Angioedema with Normal C1 Inhibitor: A Case Report

2015

Pathologymedicine.medical_specialtybiologybusiness.industryImmunologymedicine.diseaseGenetic analysisDermatologyC1-inhibitorHereditary angioedemamedicinebiology.proteinImmunology and Allergybusiness
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Definitive Link of Mutation c.351delC and Development of Hereditary Angioedema in a Large Brazilian Family

2011

S U N D A Y 381 Definitive Link of Mutation c.351delC and Development of Hereditary Angioedema in a Large Brazilian Family M. F. Ferraro, A. S. Moreno, E. Castelli, A. P. Lange, E. A. Donadi, K. Bork, W. Sarti, L. K. Arruda; School of Medicine of Ribeirao Preto, Ribeirao Preto, BRAZIL, Johannes-Gutenberg University, Mainz, GERMANY. RATIONALE:We have previously described the identification of a novel SERPING1 mutation (c.351delC) in members of a large Brazilian family with Hereditary Angioedema (HAE). In the present study, we have aimed to verify the association of this mutation with the development of HAE in this family. METHODS: Family pedigree was constructed with 275 individuals distribu…

MutationAbdominal painPediatricsmedicine.medical_specialtybiologyAngioedemabusiness.industryImmunologyDiseasemedicine.disease_causemedicine.diseaseAsymptomaticC1-inhibitorExonHereditary angioedemabiology.proteinImmunology and AllergyMedicinemedicine.symptombusinessJournal of Allergy and Clinical Immunology
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A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family

2011

To cite this article: Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family.Allergy 2011; 66: 1384–1390. Abstract Background:  Hereditary angioedema is an autosomal dominant disease characterized by episodes of subcutaneous and submucosal edema. It is caused by deficiency of the C1 inhibitor protein, leading to elevated levels of bradykinin. More than 200 mutations in C1 inhibitor gene have been reported. The aim of this study was to analyze clinical features of a large family with an index case of hereditary angioe…

GeneticsMutationbiologyAngioedemabusiness.industryImmunologyAutosomal dominant traitmedicine.diseasemedicine.disease_causeFrameshift mutationC1-inhibitorExonHereditary angioedemamedicinebiology.proteinImmunology and Allergymedicine.symptombusinessIndex caseAllergy
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Definition, aims, and implementation of GA [sup] 2 LEN/HAEi Angioedema Centers of Reference and Excellence

2020

This document summarizes the aims of GA2 LEN/HAEi Angioedema Centers of Reference and Excellence (ACAREs) and elaborates the requirements that ACAREs must fulfill to become certified. It also provides (see Appendix S1) background information on GA2LEN and HAEi, including HAEi member organizations and regional patient advocates, on why we need an Angioedema Center of Reference and Excellence (ACARE) program and network, and on the accreditation and certification process, governance and funding, and on the interaction with other GA2LEN networks of centers of reference and excellence. The protocols, aims, requirements, and provisions related to becoming a certified CARE are based on (a) the ex…

medicine.medical_specialtyEdema angioneuròticUrticariamedia_common.quotation_subjectImmunologyeducationGA2LENAngioedema; Center; Excellence; Management; Urticariaurticariacentres of reference and excelenceExcellenceimmune system diseasescentermedicineImmunology and AllergyCenter (algebra and category theory)Angioneurotic edemaskin and connective tissue diseasesmedia_commonudc:616.1Angioedemabusiness.industryangioedemahumanitiesreferenčni centri odličnostiMedicine; Allergy; ImmunologyFamily medicineexcellencemedicine.symptombusinessGlobal Allergy and Asthma European NetworkUrticàriamanagement
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Novel SERPING1 mutation causing Hereditary Angioedema in a Brazilian family

2009

Geneticsbusiness.industryImmunologyMutation (genetic algorithm)Hereditary angioedemaImmunology and AllergyMedicinebusinessmedicine.diseaseJournal of Allergy and Clinical Immunology
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