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The clinical trial and the enrollment of subjects were described previously (Werling et al., 2013b).
The two groups of subjects were described in detail elsewhere (14).
Subjects were described as XX, xx, PP, pp, homozygotes; and Xx or Pp heterozygotes.
Clinical investigation including visual acuity, age of onset in each affected subjects were described in Table 1.
These subjects were described in a previous cross-sectional study [ 11] and followed-up as a cohort (development population).
Subjects were described using descriptive statistics, such as mean (s.d)., median (interquartile range), and proportion (with 95% confidence interval).
Similar(48)
Neurological characteristics of AD and MCI subjects are described in Table 1.
Based on experimental results the influence of posture and stature on the biodynamic behaviour of human subjects is described.
The limiting distributions of the waiting time until a treatment receives the given number of subjects are described.
For this purpose, two subjects are described in this study, namely, (1) fast-tracking model creation, and (2) cross-organizational process reengineering.
We find that, when suitably rescaled, the distributions of the variations in the beat-to-beat intervals for all healthy subjects are described by a single function stable over a wide range of timescales.
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