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)...
Biopsia tiroidea nella diagnosi di linfoma: le performance diagnostiche e il ruolo dell’approccio multidisciplinare…
13.10.2023
Per confrontare l’accuratezza diagnostica delle biopsie tiroidee (CNB, core needle biopsy) e delle biopsie escissionali (SEB, surgical excision...
Variazioni dell’istologia nel linfoma di Hodgkin nodulare a predominanza linfocitaria in una popolazione adulta:…
13.10.2023
Un sottogruppo di pattern di varianti istologiche del linfoma di Hodgkin nodulare a predominanza linfocitaria (NLPHL, nodular lymphocyte-predominant...
Multi-omics analysis of multiple myeloma patients with differential response to first line treatment
09.10.2023
The genome backgrounds of multiple myeloma (MM) would affect the efficacy of specific treatment. However, the mutational and transcriptional...