L. Maia

Serum Baseline Tryptase Level as a Marker for the Severity of Anaphylaxis

L. Arruda, D. Aragon, A. Moreno, 2019, International Archives of Allergy and Immunology.

Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families.

S. Cichon, J. Pesquero, L. Arruda, 2017, The journal of allergy and clinical immunology. In practice.

Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis

D. Solé, N. Rosário, J. Pesquero, 2018, Clinics.

Gene mapping strategy for Alu elements rearrangements: Detection of new large deletions in the SERPING1 gene causing hereditary angioedema in Brazilian families.

J. Pesquero, L. Arruda, A. Grumach, 2019, Gene.

Decreasing Attacks and Improving Quality of Life through a Systematic Management Program for Patients with Hereditary Angioedema

L. Arruda, D. Aragon, Luis L. P. daSilva, 2021, International Archives of Allergy and Immunology.

Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency

S. Cichon, W. A. Silva, K. Bork, 2019, Allergy.

A cost-effective algorithm for diagnosis of hereditary angioedema with normal C1 inhibitor: applying molecular approach to clinical practice.

W. A. Silva, L. Arruda, A. Moreno, 2019, The journal of allergy and clinical immunology. In practice.

Genetic Analysis as a Practical Tool for Diagnosis of Hereditary Angioedema With Normal C1 Inhibitor: A Case Report.

E. Castelli, V. Muglia, K. Bork, 2016, Journal of investigational allergology & clinical immunology.

HLA-G Gene Variability Is Associated with Papillary Thyroid Carcinoma Morbidity and the HLA-G Protein Profile

E. Donadi, E. Castelli, L. Maciel, 2023, International journal of molecular sciences.