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ECG abnormalities will be followed up by measurement of cardiac troponin T to quantify the myocyte necrosis.
Furthermore, information on aortic and mitral valve morphology/calcification and pericardial abnormalities will be collected.
More detailed results of neurological manifestations and technical abnormalities will be published separately.
Some limb abnormalities will be more obvious, in motion, on dynamic images.
The ability to monitor wire data to determine any behavioral abnormalities will be critical in pin-pointing any lateral movement of malware, as well as potential attempts at exfiltration of sensitive data.
Acidosis and electrolyte abnormalities will be corrected as necessary.
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On occasion, a potential abnormality will be discovered during a research MR scan.
However, they do not guarantee that an abnormality will be picked up.
Women who subsequently deliver an infant with a congenital abnormality will be excluded from the study analysis.
However, the evidence would suggest that the more severe the phenotype overall, the more likely it is that a genomic abnormality will be identified [1].
As shown in Table 4, the interpretation of the specific abnormality will be influenced by the disease stage at which the patient is undergoing testing, SMM versus MM.
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