Results 221 to 230 of about 22,643,381 (355)
The Indian Experience With Nonacog Beta Pegol for the Treatment of Hemophilia B in Children and Adolescents: A Safety and Efficacy Evaluation. [PDF]
Patel N+5 more
europepmc +1 more source
Use of human factor VIIa in the treatment of two hemophilia A patients with high-titer inhibitors. [PDF]
Ulla Hedner, Walter Kisiel
openalex +1 more source
Acquired hemophilia A: Updated review of evidence and treatment guidance
R. Kruse-Jarres+7 more
semanticscholar +1 more source
ABSTRACT Background Previous work found a decrease in lysophosphatidylcholines (LPCs) in fibromyalgia (FM) serum, prompting the hypothesis that this decrease could be due to increased conversion of LPC to lysophosphatidic acid (LPA) through autotaxin (ATX). LPA has pronociceptive functions, and increased LPA levels could modulate FM pain.
Joana Menezes+10 more
wiley +1 more source
Hemophilia B in a male with a four-base insertion that arose in the germline of his mother [PDF]
C. D. K. Bottema+3 more
openalex +1 more source
ABSTRACT Background Pressure pain thresholds (PPT) are a component of Quantitative Sensory Testing and are used to assess mechanical pain sensitivity. Joint‐specific PPT measurements are relevant because many joint disorders involve altered pain processing at and around joints. This study aims to establish such reference values that might contribute to
Fabian Tomschi+3 more
wiley +1 more source
A Systematic Review of the Oral Health Status of Hemophilic Patients. [PDF]
Akitomo T+3 more
europepmc +1 more source
A Dutch family with moderately severe hemophilia B (Factor IXHeerde) has a missense mutation identical to that of factor lXLondon 2 [PDF]
S R Poort+3 more
openalex +1 more source
ABSTRACT Background A 7‐month‐old female spayed English Springer Spaniel (ESS) was evaluated for spontaneous hemoperitoneum. Hyperfibrinolysis was identified on thromboelastography. Hypothesis/Objectives To identify a genetic mutation causing congenital hyperfibrinolysis in the proband and evaluate the prevalence of the mutation in the ESS breed ...
Kelley Kilpatrick+7 more
wiley +1 more source