Evaluation of a rapid von Willebrand Factor Activity Latex Immuno Assay for monitoring of patients with von Willebrand disease (
Saravanan Vinayagam +5 more
openalex +1 more source
ABSTRACT Acquired factor V inhibitor is a rare and clinically challenging condition that can manifest across a spectrum ranging from asymptomatic laboratory abnormalities to life‐threatening hemorrhagic episodes. This case reports a patient with antibiotic‐associated AFVI, who presents asymptomatically and may be managed conservatively with close ...
Chunjuan Zhao, Weibu Chen, Xueyan Chen
wiley +1 more source
Role of plasma Von-Willebrand factor in children with chronic liver diseases. [PDF]
Behairy OGA +5 more
europepmc +1 more source
ABSTRACT Cardiac myxomas are benign tumors; however, infected myxomas represent a rare clinical presentation. Infected myxomas can cause concomitant infective valve endocarditis, which may lead to complications such as persistent bacteremia, valvular insufficiency/stenosis, and embolic phenomena if not treated promptly.
Karuna Rayamajhi +5 more
wiley +1 more source
Endothelial Cell Transition: Preliminary Data on Cross-Organ Shift from Brain to Liver. [PDF]
Larionov A, Filgueira L, Hammer CM.
europepmc +1 more source
High purity, double virus-inactivated VWF/FVIII concentrate in long term prophylaxis of von Willebrand disease - experience from prospective clinical trials and German post-licensure surveillance [PDF]
Erik Berntorp +3 more
openalex
Congenital thrombotic thrombocytopenic purpura (cTTP) is an ultra‐rare, potentially life‐threatening condition caused by a deficiency of the blood enzyme ADAMTS13. Until now, ADAMTS13 replacement has been achieved with infusions of plasma or plasma‐based therapies (PBT).
Munjal Patel +11 more
wiley +1 more source
Constitutive interaction between neutrophils and von Willebrand factor in peripheral blood. [PDF]
Wan Y +7 more
europepmc +1 more source
Fibrosis 4 Index Predicts Haemocompatibility-Related Adverse Events in Patients Using Left Ventricular Assist Devices. [PDF]
Kurihara T +18 more
europepmc +1 more source
Deficiency of nNOS in adult‐born dentate granule cells causes epilepsy
Abstract Objective This study aimed to elucidate the molecular role of neuronal nitric oxide synthase (nNOS, encoded by Nos1) in adult‐born dentate granule cells (DGCs) during temporal lobe epilepsy (TLE). Methods We used GFP‐expressing retrovirus (RV) to analyze morphological changes in DGCs.
Hanyu Huang +11 more
wiley +1 more source

