Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2020

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#MCAD-Mangel ist die häufigste der angeborenen Fettsäurenoxidationsstörungen #FAOD Hier nun eine Veröffentlichung, die schaut, wie zukünftige Forschungsstudien besser vergleichbar gemacht werden können

13 Feb 2020

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RT @CIMDRN: The first step toward establishing core outcome sets for PKU and MCAD deficiency has been published in Orphanet Journal of Rare…

13 Feb 2020

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RT @ojrarediseases: A new review on outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonu…

22 Jan 2020

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The first step toward establishing core outcome sets for PKU and MCAD deficiency has been published in Orphanet Journal of Rare Diseases: https://t.co/cummsAF0LZ

22 Jan 2020

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