Evidence map›Paper›PMID 37999237›Full record

ArticleMetabolites2023

PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening.

Melanie T Achleitner, Judith J M Jans, Laura Ebner, Johannes Spenger, Vassiliki Konstantopoulou, René G Feichtinger, Karin Brugger, Doris Mayr, Ron A Wevers, Christian Thiel and 2 more

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

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

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 4 countries.

Melanie T AchleitnerUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.
Judith J M JansDepartment of Genetics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.ORCID 0000-0003-0960-6263
Laura EbnerUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.
Johannes SpengerUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.ORCID 0000-0002-8519-1269
Vassiliki KonstantopoulouDepartment of Pediatrics, Austrian Newborn Screening, Medical University of Vienna, 1090 Vienna, Austria.
René G FeichtingerUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.ORCID 0000-0002-4215-8258
Karin BruggerUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.
Doris MayrUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.
Ron A WeversDepartment of Human Genetics, Translational Metabolic Laboratory, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.ORCID 0000-0003-2278-9746
Christian ThielCenter for Child and Adolescent Medicine, Pediatrics I, University Heidelberg, Analysezentrum 3, 69120 Heidelberg, Germany.ORCID 0000-0001-6419-8747
Saskia B WortmannUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.ORCID 0000-0002-1968-8103
Johannes A MayrUniversity Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.ORCID 0000-0001-6970-336X
Paracelsus Medical University · ATRadboud University Nijmegen · NLHeidelberg University · DEMedical University of Vienna · ATUtrecht University · NL

Funding

Austrian Science Fund FWF I 4695FWF Austrian Science Fund I4695-B
6 · The paper itself

Abstract

Two siblings showed increased galactose and galactose-related metabolites in neonatal screening. Diagnostic workup did not reveal abnormalities in any of the known disease-causing enzymes involved in galactose metabolism. Using whole-exome sequencing, we identified a homozygous missense variant in

Indexed as

galactosegalactosemiahyperbilirubinemiainborn metabolic disorderPPA1pyrophosphate

Identifiers

PMID37999237
PMCPMC10673274
OpenAlexW4388574515

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.