bachelor's at Medicina from Universidade Federal do Ceará (1982), master's at Paediatrics from Universidade Federal de São Paulo (1987) and doctorate at Medicina from Universidade Federal de São Paulo (1990). Has experience in Medicine, focusing on Allergology and Clinical Imunology, acting on the following subjects: mites, asthma, cockroach, recombinant allergens and allergens. (Source: Lattes Curriculum)
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Atopic Dermatitis (AD) is a chronic and relapsing inflammatory skin disease, characterized by intense pruritus and recurrent eczematous lesions, with prevalence varying from 0.2% to 20%. AD includes different phenotypes and endotypes, according to ethnicity, age, immune response profile, presence of loss-of-function mutation in the gene coding for filaggrin and barrier defects, infection …
Asthma in one of the most common chronic disease, with prevalences of 10% and 17% in adults and children, respectively, in Brazil. In a previous study, carried out in Primary Care Units of the North District of the City of Ribeirão Preto, we have found that asthma is underdiagnosed, and that patients frequently seek medical care only during acute exacerbations. After a year of a capacitat…
(Only some records are available in English at this moment)
Asthma is a chronic disease and an important public health problem due to its high prevalence. The disease is strongly associated with exposure to environmental allergens and genetic predisposition, and it could lead to death from an acute asthma attack. It significantly affects the quality of life of the individual, and leads to high rates of health-related expenses, so treatment is very…
Anaphylaxis is a severe, potentially fatal, allergic reaction, which generally occurs after exposure to a trigger. This clinical condition is more common than most people realize, and there is evidence that anaphylaxis is underdiagnosed and undertreated. Most common triggers include foods, drugs and venom of Hymenoptera insects (wasps, bees and ants), with variable prevalence, depending o…
Hereditary angioedema (HAE) is a rare disease with autosomal dominant inheritance, characterized by recurrent attacks of subcutaneous edema of upper airways and gastrointestinal tract. In its classic form, the HAE is caused by mutations in SERPING1 gene encoding the C1 inhibitor (C1-INH). HAE Type I results from the quantitative deficiency of C1-INH, whereas HAE type II is characterized b…
(Only some records are available in English at this moment)
Hereditary angioedema (HAE) is a rare disease with autosomal dominant inheritance, characterized by recurrent episodes of swelling of face, extremities and larynx, and attacks of abdominal pain. In its classic form, the HAE is caused by mutations in SERPING1, the gene encoding C1 inhibitor (C1-INH), and results from the quantitative and/or qualitative deficiency of C1-INH (HAE-C1-INH). Mu…
| 1 / 1 | Ongoing research grants |
| 15 / 11 | Completed research grants |
| 21 / 6 | Completed scholarships in Brazil |
| 1 / 1 | Completed scholarships abroad |
| 39 / 20 | All research grants and scholarships |
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CV Lattes
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