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Samples were stored at −80 °C for further analyses using a validated ELISA (Intertek dba ALTA Analytical Laboratory, San Diego, CA, USA) 21.
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Plasma samples of docetaxel were analysed using a validated specific liquid chromatography-mass spectrometry (LC-MS/MS) method as described previously (Agus et al, 2005).
All statistical analyses were performed using a validated statistical software, Stata Version 10.0.
Drug analyses were performed as described previously using a validated high performance liquid chromatographic method with column switching and spectrophotometric detection [ 33].
QoL was assessed using a validated scale.
(R -11C]verapamil data weR -11C]verapamilg a previously validatad constrained twereissue companalysedplasma inpusingdel [28].
Data were then integrated and analysed using a previously validated CHD model.
We also conducted our analyses using a relatively large cohort of individuals with complete, comprehensive demographic information and validated survey measures.
All data sets were analysed using a previously presented and validated method.
Data were analysed using a Bayesian approach (BADGE), and validated with quantitative real-time PCR (qPCR) in 31 independent NlEpi samples from 8 RM, 17 HN, and 6 PM patients.
To validate the numerical results, the designed lens is analysed using a full-wave EM-solver.
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