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The Italian National Survey for PraderWilli syndrome: An epidemiologic study

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A second Phase 3 trial, TRANSCEND-T2D-1 (type 2 diabetes population), showed dramatically lower rates: 4.4% at 12 mg

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Then, we evaluated L-carnitine-attributed effects by comparing VPA elimination half-lives and time-courses of blood lactate levels and organ dysfunction [assessed by the Sequential Organ Failure Assessment (SOFA) score] between matched L-carnitine-treated and non-treated patients using a multivariate analysis including a propensity score Results Sixty-nine VPA-poisoned patients (40F/29 M