Nathália Cagini

Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. Instituto Nacional de Farmacologia (INFAR) (Institutional affiliation from the last research proposal)
Birthplace: Brazil

Abstract
Hereditary angioedema (HAE) is characterized by sudden episodes of swelling that cause pain, discomfort, and according to its location can cause disfigurement of the individual. Edema affects mainly the upper and lower extremities, gastrointestinal tract, genitalia and face. If not treated it can lead to death due to laryngeal edema HAE is an autosomal dominant disorder resulting from mut…
Functional caracterization of the p.G184R, p.A297T, p.L251P, p.A457P and p.F477L variants found in the C1 esterase inhibitor gene - SERPING1, BP.DR
Abstract
The hereditary angioedema (HAE) is characterized by repetitives episodes of painful edemas, discomfort and according to their location can cause disfigurement of the individual. The edemas affect mainly the upper and lower extremities, gastrointestinal tract, genitals and face. If untreated, it can lead to death due to laryngeal edema. The HAE is an autosomal dominant disorder resulting f…
Standardizing a methodology to sequence Factor XII, C1 inhibitor esterase (C1INH) and kinin B2 receptor genes. Analysis of the relationship between the mutations in these three genes with the symptoms of Hereditary Angioedema (HAE), BP.MS

Source:Lattes Curriculum

CV Lattes

2 / 2	Completed scholarships in Brazil

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Abstract

Abstract