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In fact, the behavior of inhibited FXIII(a) (in this case by EA) in term of lacking changes in APTT, PT, and TT is similar to what have been reported for patients with FXIII genetic deficiency [14, 15]
How patients were involved in the creation of this article This article has been shared with Martyn Hooper, chairperson of the Pernicious Anaemia Society (PAS), for comments and feedback
A high-dose corticosterone determined based on Experiment I (400 M) was selected for subsequent assays of oxidative stress
Scopolamine patch: For severe refractory nausea
AMPK regulates the circadian clock by cryptochrome phosphorylation and degradation
Analysis of case-parent trios at a locus with a deletion allele: Association of GSTM1 with autism
