Luana M. Maia

Av. Bandeirantes, 3900, Monte Alegre, Ribeirão Preto
Sao Paulo, SP 14049900, Brazil

Last Updated: 09/26/2026

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Found 10 publications

Insights From the First 820 Patients From the Brazilian Multicenter Registry of Hereditary Angioedema: The Key Role of Genetic Testing and Targeted Therapies.

Insights From the First 820 Patients From the Brazilian Multicenter Registry of Hereditary Angioedema: The Key Role of Genetic Testing and Targeted Therapies.

Journal: The journal of allergy and clinical immunology. In practice

Published: June 06, 2025

Recessive SERPING1 Variant Leads to Kinin-Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema.

Recessive SERPING1 Variant Leads to Kinin-Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema.

Journal: Journal of clinical medicine

Published: October 31, 2023

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

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

Journal: International journal of molecular sciences

Published: July 16, 2023

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

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

Journal: International archives of allergy and immunology

Published: October 20, 2020

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

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

Journal: The journal of allergy and clinical immunology. In practice

Published: March 10, 2019

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

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

Journal: Allergy

Published: December 18, 2018

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

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

Journal: International archives of allergy and immunology

Published: December 01, 2018

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

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

Journal: Gene

Published: July 30, 2018

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

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

Journal: Clinics (Sao Paulo, Brazil)

Published: August 02, 2017

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

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

Journal: The journal of allergy and clinical immunology. In practice

Published: June 02, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026