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Rosemeire Navickas Constantino-Silva

Showing results (1-10 of 7) with videos related to

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Frontiers in Medicine|May 7, 2019
Hereditary Angioedema-Associated Acute Pancreatitis in C1-Inhibitor Deficient and Normal C1-Inhibitor Patients: Case Reports and Literature ReviewCamila Lopes Veronez, Régis Albuquerque Campos, Rosemeire Navickas Constantino-Silva, et al.
Journal of Clinical Immunology|June 6, 2015
A homozygous CARD9 mutation in a Brazilian patient with deep dermatophytosisAnete S Grumach, Flavio de Queiroz-Telles, Mélanie Migaud, et al.
Biological Chemistry|January 12, 2016
Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencingCamila Lopes Veronez, Elton Dias da Silva, Patrícia Varela Lima Teixeira, et al.
Frontiers in Immunology|September 11, 2025
Evaluating functional C1INH with multiple laboratory methods across Hereditary Angioedema typesMaine Luellah Demaret Bardou, Rosemeire Navickas Constantino-Silva, Maria Luiza Oliva Alonso, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 13, 2017
Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian FamiliesCamila Lopes Veronez, Adriana S Moreno, Rosemeire Navickas Constantino-Silva, et al.
The Journal of Allergy and Clinical Immunology. in Practice|October 12, 2025
Real-World Evidence on the Management of Hereditary Angioedema With Normal C1 InhibitorNyla Thyara Melo Lobão, Maine Luellah Demaret Bardou, Shirley Yajaira Cerinza Vila, et al.
International Archives of Allergy and Immunology|January 28, 2021
The Challenges in the Follow-Up and Treatment of Brazilian Children with Hereditary AngioedemaJoanna Araújo-Simões, Aline Gisele Pena Boanova, Rosemeire Navickas Constantino-Silva, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Frontiers in Medicine|May 7, 2019
Hereditary Angioedema-Associated Acute Pancreatitis in C1-Inhibitor Deficient and Normal C1-Inhibitor Patients: Case Reports and Literature ReviewCamila Lopes Veronez, Régis Albuquerque Campos, Rosemeire Navickas Constantino-Silva, et al.
Journal of Clinical Immunology|June 6, 2015
A homozygous CARD9 mutation in a Brazilian patient with deep dermatophytosisAnete S Grumach, Flavio de Queiroz-Telles, Mélanie Migaud, et al.
Biological Chemistry|January 12, 2016
Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencingCamila Lopes Veronez, Elton Dias da Silva, Patrícia Varela Lima Teixeira, et al.
Frontiers in Immunology|September 11, 2025
Evaluating functional C1INH with multiple laboratory methods across Hereditary Angioedema typesMaine Luellah Demaret Bardou, Rosemeire Navickas Constantino-Silva, Maria Luiza Oliva Alonso, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 13, 2017
Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian FamiliesCamila Lopes Veronez, Adriana S Moreno, Rosemeire Navickas Constantino-Silva, et al.
The Journal of Allergy and Clinical Immunology. in Practice|October 12, 2025
Real-World Evidence on the Management of Hereditary Angioedema With Normal C1 InhibitorNyla Thyara Melo Lobão, Maine Luellah Demaret Bardou, Shirley Yajaira Cerinza Vila, et al.
International Archives of Allergy and Immunology|January 28, 2021
The Challenges in the Follow-Up and Treatment of Brazilian Children with Hereditary AngioedemaJoanna Araújo-Simões, Aline Gisele Pena Boanova, Rosemeire Navickas Constantino-Silva, et al.
Pageof 1