Importancia del diagnóstico de portadoras en familias con antecedentes de hemofilia
La hemofilia es una enfermedad hemorrágica hereditaria ligada al cromosoma X que se presenta debido a mutaciones en los genes del factor VIII (hemofilia A) y el factor IX (hemofilia B), que ocasiona una disminución o deficiencia funcional de estas ...
Kalia Lavaut Sánchez
doaj
[Application of gene therapy in the treatment of hematological diseases: achievements, and economic and ethical aspects of the topic]. [PDF]
Diaz-Garcia H +2 more
europepmc +1 more source
Effect of DNA methylation on inhibitor development in people with hemophilia A treated with FVIII concentrates. [PDF]
Chand H +5 more
europepmc +1 more source
Cirurgia e Hemofilia com Inibidor: 4 Casos Clínicos [PDF]
Antunes, M, Diniz, MJ, Santos, A
core
Hemophilic Pseudotumor of the Maxilla Secondary to Endodontic Treatment: Case Report and Systematic Review. [PDF]
Quiroz-Gomez JR +5 more
europepmc +1 more source
Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy Carriers. [PDF]
Vigliano AP +10 more
europepmc +1 more source
F8/F9 variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation Project. [PDF]
Labarque V +5 more
europepmc +1 more source

