CV Lattes
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Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. Escola Paulista de Medicina (EPM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Graduated at the medical school from Universidade Federal do Espírito Santo (2004) and fellow in Internal Medicine (2007) and rheumatology (2009) at Universidade Federal de São Paulo. PhD in rheumatology at Universidade Federal de São Paulo. Postodoctoral at the University of Washington and fellowship in Seattle Children's Research Institute/Center for immunity and immunotherapies. Currently holds the following positions: Affiliated Professor and chief of the Immune dysregulation Clinics of the Rheumatology Division at Universidade Federal de São Paulo; Physician of the Immunology Division of the Central Laboratory at Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo; Dean of the Rare Diseases Commitee of the Brazilian Rheumatology Society; Member of the Midia Commitee of the Paulista Rheumatology Society. Has experience in Medicine, focusing on Internal Medicine and Rheumatology, acting on the following subjects: immune dysregulation, primary immune regulatory diseases, autoinflammatory diseases, autoimmune rheumatic diseases, systemic lupus erythematosus, Behçets disease, immunodeficiency, immunology, rheumatoid arthritis. (Source: Lattes Curriculum)
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Behçet's Disease (BD) is currently classified as a polygenic autoinflammatory syndrome. Recently point mutations in NFKB1, TNFAIP3 and NEMO were associated with BD-like phenotypes, showing the importance of the NF-kB pathway on BD pathogenesis. Constitutional or acquired trisomy 8, which encodes IKBKB, an important NF-kB activator, is often associated with BD. In addition, sCD40L, which, …
Primary Immune Regulation Disorders (PIRD) comprise a set of genetic conditions that impact the regulation of the immune system. In the context of pediatric patients, the imbalance in the immune system's defense against pathogens can lead to recurrent infections, autoimmunity, and chronic inflammation. Medical research has identified new PIRD, and understanding these complex conditions is…
Although still considered rare conditions, the universe of Primary Immunoregulatory Disorders (PIRDs) is exponentially expanding as a unique group. The concurrent presence of autoimmune manifestations is frequent; however, the literature remains sparse regarding immunomediated rheumatic conditions. Considering the importance of early diagnosis, the description of clinical phenotypes, and …
Behçet's disease (BD) is currently classified as a polygenic autoinflammatory syndrome. Recently point mutations in NFKB1, TNFAIP3 and NEMO were associated with BD-like phenotypes, showing the importance of the NF-kB pathway on BD pathogenesis. Constitutional or acquired trisomy 8, which encodes IKBKB, an important NF-kB activator, is often associated with BD. In addition, sCD40L, which, …
(Only some records are available in English at this moment)
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| 5 / 5 | Completed scholarships in Brazil |
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