Lilian Pereira Ferrari
Biographic Data
| ID | 8566803 |
|---|---|
| NAME | Lilian Pereira Ferrari |
| GIVEN NAMES | Lilian Pereira |
| FAMILY NAME | Ferrari |
| SIGNATURE | FERRARI L P |
| AFFILIATIONS | Universidade Federal do Rio Grande do Sul |
| ORCID | 0000-0001-8680-8200 |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2024 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 0 |
Analysis of the relationship between genetic mutation, clinical manifestations and prognosis in hereditary angioedema
Hereditary Angioedema (HAE) is a rare and severe genetic autosomal dominant disease of the immune system, caused by a deficiency of C1 esterase inhibitor (C1-INH). Classified into 3 subtypes: HAE with quantitative deficiency of the C1-INH inhibitor, C1-INH dysfunction, and normal C1-INH.The objective is to present a protocol examining the evidence on the relationship between mutations, clinical manifestations and prognosis in AEH. A systematic re…
No prominent works on this page.
Analysis of the relationship between genetic mutation, clinical manifestations and prognosis in hereditary angioedema
Hereditary Angioedema (HAE) is a rare and severe genetic autosomal dominant disease of the immune system, caused by a deficiency of C1 esterase inhibitor (C1-INH). Classified into 3 subtypes: HAE with quantitative deficiency of the C1-INH inhibitor, C1-INH dysfunction, and normal C1-INH.The objective is to present a protocol examining the evidence on the relationship between mutations, clinical manifestations and prognosis in AEH. A systematic re…
Angioedema (1 work) · Biology (1 work) · Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 work) · Dermatology (1 work) · Genetics (1 work) · Hemophilia Treatment and Research (1 work) · Hereditary angioedema (1 work) · Medicine (1 work) · Mutation (1 work) · Vitamin K Research Studies (1 work)