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Total creep feed consumption during lactation was higher for the PF than for the CF (PF: 202 ± 23 vs. CF: 118 ± 17; P = 0.0022).
The risk of CAD is not typically considered as an active alternative diagnosis for the CF patient; yet with aging, even CF patients will be at risk for CAD.
Cystic fibrosis (CF) is caused by mutations in the gene encoding for the CF transmembrane conductance regulator (CFTR) protein, which acts as a chloride channel after activation by cyclic AMP (cAMP).
The solution for the CF power allocation problem can be derived equivalently to the AF case.
c Photograph and SPECT/CT image of the plastic bottle used for the CF quality control.
In this section, we give some important results for the CF Dirac system on (mathbb{T}).
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This chapter focuses on the development of a composite-bonded doubler as an enhancement for the CF-116 upper wing skin.
Negative values were also observed for the cf-AC-AuNPs (−27.15~−30.27 mV); however, the zeta potential values of the cf-AC-AuNPs showed no general tendency.
Aiming for the best possible quality of life for the CF-patients, OPAT was introduced and the goal is to minimize the complications experienced during OPAT.
The greatest discrepancy (for one subject) was 4. The intra-class correlation coefficient for the CF-QOL was = 0.83; 95% CI (0.68 to 0.91).
The test-retest reproducibility using the intra-class correlation coefficient (ICC) for the CF-QOL was 0.83, 95% confidence interval 0.68 to 0.91.
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