1 min
23.10.2025
Abstract Mutations responsible for mild/moderate hemophilia A were extensively characterized over the last 15 years and more than 200 mutations have...
Laboratory diagnosis of von Willebrand disease in the age of the new guidelines: considerations based on geography and…
1 min
23.10.2025
Abstract von Willebrand disease (VWD) is considered the most common bleeding disorder and arises from deficiency and/or defect in the adhesive plasma...
Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine…
1 min
23.10.2025
Abstract Hemophilia A and hemophilia B are rare congenital, recessive X-linked disorders caused by lack or deficiency of clotting factor VIII (FVIII)...
Dealing with IGs Shortages: A Rationalization Plan
2 min
14.06.2024
BACKGROUND: La domanda e il consumo di immunoglobuline (IgG) sono in crescita e ci sono molte difficoltà di approvvigionamento. Lo scopo dello studio...
B- and T- Cell Subset Abnormalities in Monogenic CVID
14.06.2024
L'immunodeficienza comune variabile (CVID) è un gruppo eterogeneo di errori congeniti dell'immunità caratterizzati da ridotte concentrazioni sieriche...
An Expert Opinion: Approach for Gastrointestinal Manifestations of CVID
13.06.2024
L'immunodeficienza comune variabile (CVID) è l'immunodeficienza primaria sintomatica più comune. È caratterizzata da un’alterata differenziazione dei...