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Comment
. 2021 Aug;148(2):e2021051020.
doi: 10.1542/peds.2021-051020. Epub 2021 Jul 15.

Following Patients With Inborn Errors of Metabolism: What Do We Value and How Do We Know?

Jeffrey P Brosco  1 , Cynthia F Hinton  2
Affiliations
Comment

Following Patients With Inborn Errors of Metabolism: What Do We Value and How Do We Know?

Jeffrey P Brosco et al. Pediatrics. 2021 Aug.
No abstract available

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Conflict of interest statement

POTENTIAL CONFLICT OF INTEREST: The authors have no conflicts of interest to disclose.

Comment on

  • Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Phenylketonuria.
    Pugliese M, Tingley K, Chow A, Pallone N, Smith M, Chakraborty P, Geraghty MT, Irwin JK, Mitchell JJ, Stockler S, Nicholls SG, Offringa M, Rahman A, Tessier LA, Butcher NJ, Iverson R, Lamoureux M, Clifford TJ, Hutton B, Paik K, Tao J, Skidmore B, Coyle D, Duddy K, Dyack S, Greenberg CR, Jain Ghai S, Karp N, Korngut L, Kronick J, MacKenzie A, MacKenzie J, Maranda B, Potter M, Prasad C, Schulze A, Sparkes R, Taljaard M, Trakadis Y, Walia J, Potter BK; Canadian Inherited Metabolic Diseases Research Network. Pugliese M, et al. Pediatrics. 2021 Aug;148(2):e2020037747. doi: 10.1542/peds.2020-037747. Epub 2021 Jul 15. Pediatrics. 2021. PMID: 34266901

References

    1. COMET Initiative. Available at: https://www.comet-initiative.org/. Accessed April 1, 2021
    1. Pugliese M, Tingley K, Chow A, et al. Core outcome sets for medium chain Acyl-coA dehydrogenase deficiency and phenylketonuria. Pediatrics. 2021;148(2): e2020037747. - PubMed
    1. Paul D, Brosco JP. The PKU Paradox: A Short History of a Genetic Disease. Balti-more, MD: The Johns Hopkins University Press; 2013:111–139
    1. Powell CM. Newborn screening and long-term outcomes. Pediatrics. 2020;146(5): e2020023663. - PubMed
    1. Kemper AR, Boyle CA, Brosco JP, Grosse SD. Ensuring the life-span benefits of newborn screening. Pediatrics. 2019;144(6): e20190904. - PMC - PubMed

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