Detection of inborn errors of metabolism in the newborn.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

1. Carnitine supplementation for inborn errors of metabolism.The Cochrane database of systematic reviews · 2012
   Pooled it
2. Inherited metabolic disorders: presentation, clinical types, laboratory diagnosis and genetic markers.Orphanet journal of rare diseases · 2025
   Review
3. [Expert consensus on the diagnosis and treatment of neonatal hyperammonemia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
   Article
4. Biochemical testing for inborn errors of metabolism: experience from a large tertiary neonatal centre.European journal of pediatrics · 2022
   Article
5. A narrative review of metabolomics in the era of "-omics": integration into clinical practice for inborn errors of metabolism.Translational pediatrics · 2022
   Review
6. Inborn Errors of Metabolism in the Era of Untargeted Metabolomics and Lipidomics.Metabolites · 2019
   Review
7. Hyperammonaemia in classic organic acidaemias: a review of the literature and two case histories.Orphanet journal of rare diseases · 2018
   Review
8. Conjugated hyperbilirubinemia presenting in first fourteen days in term neonates.World journal of hepatology · 2017
   Article
9. Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I.Blood · 2015
   Article
10. Molecular Genetics and Metabolism Report Long-term follow-up of post hematopoietic stem cell transplantation for Hurler syndrome: clinical, biochemical, and pathological improvements.Molecular genetics and metabolism reports · 2015
    Article
11. Therapies for the bone in mucopolysaccharidoses.Molecular genetics and metabolism · 2015
    Review
12. Impact of enzyme replacement therapy and hematopoietic stem cell transplantation in patients with Morquio A syndrome.Drug design, development and therapy · 2015
    Review
13. Neonatal neuroimaging findings in inborn errors of metabolism.Journal of magnetic resonance imaging : JMRI · 2013
    Review
14. Renal sonographic findings of type I glycogen storage disease in infancy and early childhood.Pediatric radiology · 2005
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

3 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as