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Clinical correlation is needed.
While the histology is suggestive of poly-lactic acid, clinico-pathologic correlation is needed for confirmation.
To calculate this sampling variance, the pretest-posttest scores correlation is needed.
It can also be elevated in other glycogen storage diseases and clinical correlation is needed.
Also, further research and histopathological correlation is needed to evaluate the role of DE-CMR in differentiating subacute from organised clots.
Clinical correlation is needed for VIEBs and other molecular indicators of risk so that targets in addition to the ER can also be more efficiently studied.
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Accurate estimates of mean nutrient composition of feeds, nutrient variance (i.e., standard deviation), and covariance (i.e., correlation) are needed to develop a more quantitative approach of formulating diets to reduce risk and optimize safety factors.
Larger studies with arthroscopic correlation are needed to explore how the normal UTE signal pattern changes with disease and injury.
In addition, further studies with arthroscopic correlation are needed to explore the role of clinical UTE sequences in the MR imaging assessment of cartilage lesions.
However, parallel comparisons between in vitro and in vivo drug responses to establish their exact correlation are needed.
Establishing such correlations is needed before additional statistical techniques can be applied to syndromic data streams to identify their early warning potential.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com