Evidence map›Paper›PMID 29234995›Full record

ArticleJournal of inherited metabolic disease2018

Correction to: Impact of age at onset and newborn screening on outcome in organic acidurias.

Jana Heringer, Vassili Valayannopoulos, Allan M Lund, Frits A Wijburg, Peter Freisinger, Ivo Barić, Matthias R Baumgartner, Peter Burgard, Alberto B Burlina, Kimberly A Chapman and 11 more

Open access · greenAbstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Journal of inherited metabolic disease, 2018. 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
–field-weighted citation impact, top 80% 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, 8 citations in OpenAlex.

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

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 17 institutions in 12 countries.

Jana HeringerDepartment of General Pediatrics, Division of Neuropediatrics and Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Im Neuenheimer Feld 430, D-69120, Heidelberg, Germany.
Vassili ValayannopoulosAssistance Publique-Hôpitaux de Paris, Centre de Référence de Maladies Métaboliques (MaMEA), Hôpital Universitaire Necker-Enfants Malades and Insitut MAGINE, Paris, France.
Allan M LundCentre for Inherited Metabolic Diseases, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Frits A WijburgDepartment of Pediatrics, Academic Medical Center, Amsterdam, Netherlands.
Peter FreisingerKlinikum am Steinenberg, Klinik für Kinder- und Jugendmedizin, Reutlingen, Germany.
Ivo BarićSchool of Medicine, University Hospital Center Zagreb and University of Zagreb, Zagreb, Croatia.
Matthias R BaumgartnerDivision of Metabolism and Children's Research Centre, University Children's Hospital Zurich, Steinwiesstraße 75, CH-8032, Zurich, Switzerland.
Peter BurgardDepartment of General Pediatrics, Division of Neuropediatrics and Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Im Neuenheimer Feld 430, D-69120, Heidelberg, Germany.
Alberto B BurlinaU.O.C. Malattie Metaboliche Ereditarie, Azienda Ospedaliera di Padova, Padova, Italy.
Kimberly A ChapmanChildren's National Medical Center, 111 Michigan Avenue, N.W., Washington, DC, 20010, USA.
Elisenda Cortès I SaladelafontHospital San Joan de Deu, Servicio de Neurologia and CIBERER, ISCIII, Barcelona, Spain.
Daniela KarallClinic for Pediatrics I, Inherited Metabolic Disorders, Medical University of Innsbruck, Innsbruck, Austria.
Chris MühlhausenKlinik für Kinder- und Jugendmedizin, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Victoria RichesBirmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
Manuel SchiffReference Center for Inborn Errors of Metabolism, APHP, University Paris-Diderot and INSERM U1141, Robert-Debré Hospital, Paris, France.
Jolanta Sykut-CegielskaScreening Department, Institute of Mother and Child, Warsaw, Poland.
John H WalterWillink Biochemical Genetics Unit, Genetic Medicine, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.
Jiri ZemanFirst Faculty of Medicine, Charles University and General University of Prague, Prague, Czech Republic.
Brigitte ChabrolCentre de Référence des Maladies Héréditaires du Métabolisme, Service de Neurologie, Hôpital d'Enfants, CHU Timone, Marseilles, France.
Stefan KölkerDepartment of General Pediatrics, Division of Neuropediatrics and Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Im Neuenheimer Feld 430, D-69120, Heidelberg, Germany. Stefan.Koelker@med.uni-heidelberg.de.
Additional individual contributors of the E-IMD consortium
Assistance Publique – Hôpitaux de Paris · FRUniversity Hospital Heidelberg · DEAcademic Medical Center · NLAzienda Ospedaliera di Padova · ITBirmingham Children's Hospital · GBCentre for Biomedical Network Research on Rare Diseases · ESChildren's National · USGeneral University Hospital in Prague · CZHeidelberg University · DEHôpital d'Enfants · FRKreiskliniken Reutlingen · DERigshospitalet · DKUniversität Innsbruck · ATUniversity Children's Hospital Zurich · CHUniversity Medical Center Hamburg-Eppendorf · DEUniversity of Manchester · GBUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to an unfortunate error during the typesetting process, the collaborators were presented incorrectly.

Identifiers

PMID29234995
OpenAlexW2771919983

What OpenQuestion holds

Textmetadata
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.