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All patients or their legal guardians received written information concerning the study and gave written informed consent for participation.
Next is the concern regarding the power of the study, given the small sample size.
All volunteers received oral and written information concerning the study prior to giving written, informed consent.
All participants received oral and written information concerning the study prior to giving their written informed consent.
Patients or their legal representatives received written information concerning the study and were asked to give written informed consent for participation.
BMB: was involved in the conception and design of the study, coordinated the study, gave structural advice concerning the statistical analysis and helped to draft the manuscript.
All the patients included in the study gave their consent concerning the treatment that is appropriate for hypovitaminosis D. Furthermore, the physicians were free to follow treatment recommendations.
JRA: was involved in the conception and design of the study, gave structural advice concerning the statistical analysis and delivered an important intellectual content regarding the revision of manuscripts.
DO gave advice concerning the study design.
UK gave substantial input concerning the study design and participated in manuscript preparation.
Participants were given written information and verbal explanation concerning the study.
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