Luana Sella Motta Maia
CV Lattes
Universidade de São Paulo (USP). Faculdade de Medicina de Ribeirão Preto (FMRP) (Institutional affiliation for the last research proposal) Birthplace: Brazil
bachelor's at Biomedicina from Centro Universitário Barão de Mauá (2004). Has experience in (Source: Lattes Curriculum)
- Hereditary Angioedema due to C1 inhibitor deficiency: characterization of mutations on SERPING1 gene, clinical correlations and investigation of ancestry, BP.DR
Abstract
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...
- Genotype-phenotype correlations in patients with hereditary angioedema, BE.EP.DR
Abstract
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). ...
| 2 / 1 | Completed scholarships in Brazil |
| 1 / 1 | Completed scholarships abroad |
| 3 / 2 | All Scholarships |
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