Biomarkers of Endothelial Damage and Disease Severity in COVID-19 Patients. [PDF]
Tsiatsiou P+11 more
europepmc +1 more source
How I treat patients with von Willebrand disease [PDF]
Pier Mannuccio Mannucci
openalex +1 more source
Willebrand factor in von Willebrand's disease. [PDF]
F E Boulton, M J Lloyd
openaire +3 more sources
Bleeding Complications in JAK2‐Variant Essential Thrombocythemia: A Revisit in 2025
ABSTRACT Essential thrombocythemia (ET) is a myeloproliferative neoplasm characterised by sustained thrombocytosis. Paradoxically, bleeding complications remain an under‐recognised clinical challenge. Compared with CALR‐mutated patients, those harbouring the JAK2‐V617F variant appear more prone to haemorrhage.
Gerard Gurumurthy+4 more
wiley +1 more source
2025 ASH ISTH NBDF WFH monitoring report on the 2021 clinical guidelines on the diagnosis and management of von Willebrand disease. [PDF]
James PD, Flood VH, Connell NT.
europepmc +1 more source
Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins [PDF]
Imre Bodó+5 more
openalex +1 more source
ABSTRACT Objectives The present study investigated the effects of thrombosis, hemorrhagic events, disease progression, and secondary malignancies on patient survival after the diagnosis of essential thrombocythemia (ET). Methods We analyzed data from 1152 patients enrolled in the JSH‐MPN‐18 study using time‐dependent Cox regression and multistate ...
Yoshinori Hashimoto+24 more
wiley +1 more source
Endothelial function and vascular events in patients with limited cutaneous systemic sclerosis (EFVELSS): a prospective observational study. [PDF]
Jud P+19 more
europepmc +1 more source
Force-induced on-rate switching and modulation by mutations in gain-of-function von Willebrand diseases. [PDF]
Kim J, Hudson NE, Springer TA.
europepmc +1 more source