Results 211 to 220 of about 151,232 (337)
ABSTRACT Aim Identifying interactors in sensorimotor processing and neurotransmission remains a current challenge for understanding neural information processing and brain function. Methods To evaluate the role of p11 in sensorimotor processing and excitatory synaptic neurotransmission, neuron‐specific lentivirus‐directed p11 silencing, small ...
Esther Vilches‐Herrando +7 more
wiley +1 more source
Type 3 von Willebrand disease in Ethiopia: a comprehensive literature review and report of the first three cases. [PDF]
Arega G +7 more
europepmc +1 more source
Screening of Von Willebrand Disease in Iranian Women With Menorrhagia
Nahid Rahbar +3 more
openalex +1 more source
Diagnostic approach to von Willebrand disease.
C. Ng, D. Motto, J. Di Paola
semanticscholar +1 more source
Avascular Necrosis and Minimal Trauma Fractures in Telomere Biology Disorders
Avascular Necrosis (AVN) and Minimal Trauma Fractures (MTF) cause significant morbidity in people with Telomere Biology Disorders (TBDs). They occur more frequently in young patients and in those with autosomal recessive (AR) or X‐linked recessive (XLR) than in autosomal dominant (AD) genotypes.
Arman M. Niknafs +3 more
wiley +1 more source
Characteristics and posttransplant outcomes of patients with congenital and acquired von Willebrand disease and hemophilia A and with renal transplants. [PDF]
Chang IW, Truman M, Yee C, Padrnos L.
europepmc +1 more source
State of the art: von Willebrand disease
Andra H. James +2 more
semanticscholar +1 more source
ABSTRACT Relapsed/refractory (R/R) mantle cell lymphoma (MCL) remains a therapeutic challenge, particularly in patients with high‐risk features or prior exposure to Bruton's tyrosine kinase inhibitors (BTKis). The advent of T‐cell–redirecting immunotherapies, including chimeric antigen receptor T‐cell (CAR‐T) therapy and bispecific antibodies (BsAbs ...
Santino Caserta +10 more
wiley +1 more source
Rewriting the script: gene therapy and genome editing for von Willebrand Disease. [PDF]
Barraclough A +8 more
europepmc +1 more source
Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype [PDF]
Giancarlo Castaman +7 more
openalex +1 more source

