Repositório Institucional da UFMG
metadata only
Aspectos clínicos, genéticos e imunológicos dos pacientes com hemofilia A grave e moderadamente grave com anticorpos inibitórios contra o fator VIII
Hemophilia A (HA) is a hereditary bleeding disoder characterized by deficiency of coagulation factor VIII (FVIII) resulting from mutations in the gene F8. Bleeding is the main clinical manifestation of the disease and is inversely proportional to the level of residual FVIII activity. Replacement of
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- De haemorrhoidibus#496073
- Genetic Profile of Alpha Thalassemia Children at Sohag University Hospital .#857962
- Los afectos y el modo de hacer filosofía inculturada#709561
- The Burden of Atypical Hemolytic Uremic Syndrome and The Clinical Characteristics of Patients in Egyptian Hospitals A Multicenter, Observational, Retrospective Cohort Study in Egypt#1047102
- Diseño y desarrollo de un catéter subcutáneo para hemodiálisis a través de la vena innominada derecha#675132
Record · ID 989552
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive