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Understanding the lack of utility of IGF-1 in assessing growth parameters in the pediatric Cushing syndrome population is important for physicians caring for these patients who should not use IGF-1 for diagnostic or treatment decisions

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14,15 In brief, both were phase III multicenter trials, double-blind and placebo-controlled to 16 weeks, assessing the efficacy and safety of bimekizumab in patients with active PsA who were bDMARD-nave or TNFi-IR

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