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Clinical response, evaluated post-treatment, was rated as cure (complete resolution of all signs and symptoms of pneumonia), improvement, or lack of progression for all abnormalities on chest radiograph [ 11].
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The significant hazard ratios were as follows: for PC1 (all abnormalities except blood pressure) 1.66 (P = 0.036), PC2 (high blood pressure levels, high HDL cholesterol) 1.71 (P = 0.016), and PC4 (low HDL cholesterol, high insulin sensitivity, low triglycerides) 2.0 (P = 0.001).
However, at doses of <50 mGy, the risk of radiation-induced abnormality is considered negligible compared with baseline risks for all developmental abnormalities, e.g., 1 % for mental retardation and 3%% for spontaneous birth defects [ 12, 14].
The comparative DR for all chromosomal abnormalities is unknown.
The Northern [19] scoring system (Table 2) gives an integrated score for all pulmonary abnormalities for each of the four lung quadrants.
The degree of improvement was for all CT abnormalities significantly different from the degree of change in the non-responders.
The age- and gender-adjusted rates for all metabolic abnormalities were higher for those living in urban areas compared with those living in rural areas.
These may possess similar caveats as genomic DNA sequencing of a selected gene but could also provide a standard method to test any subject for all sequencing abnormalities.
Thereafter, all abnormalities resolved spontaneously except for insulin-requiring diabetes.
The myometrium was thoroughly evaluated for any abnormalities in all planes.
The use of ritonavir-boosted PI regimens was associated with a consistent risk factor for all metabolic abnormality outcomes [ 20].
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