Bockenstedt explained why she felt the evidence for PMR was compelling.

This indicates that PRL is not a pro-inflammatory stimulus in patients with PMR.

Conclusion: 18F-FDG uptake distribution patterns and morphology can contribute to the diagnosis of PMR.

To begin with, women are four times more likely to get PMR than men.

No investigation of PMR of THC in human blood has been reported to date.

Using this technique, time-dependent PMR of morphine and its metabolites was investigated in 12 cases.

Because the OS of patients with NMR and PMR was similar, they were grouped together.

A trend was observed for greater PMR with increasing postmortem interval between death and sampling.

However, PMR is a severe disease with a mortality rate as high as 26%.

Serial determinations performed in 18 PMR patients showed that the antibody titer did not change significantly.

Results: A definitive diagnosis of PMR was given to 16 of 60 patients.

The aim of this study was to quantify the risk of fracture among patients with PMR and GCA.

The PMR+TD also increased plasma nonesterified fatty acids and decreased blood urea nitrogen across the day.

The purpose of this study was to identify the patterns of 18F-FDG uptake that suggest the diagnosis of PMR.

We evaluated early outcomes of PMR by using data from the Japan Cardiovascular Surgery Database, a nationwide Japanese registry.

Conclusions: This study reports, for the first time, a similar increase in fracture risk for patients with PMR and GCA.