Evidence map›Paper›PMID 27498540›Full record

ArticleJournal of inherited metabolic disease2016

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies.

Eva Morava, Vera Tiemes, Christian Thiel, Nathalie Seta, Pascale de Lonlay, Hans de Klerk, Margot Mulder, Estela Rubio-Gozalbo, Gepke Visser, Peter van Hasselt and 21 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Journal of inherited metabolic disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. What is new in CDG?Journal of inherited metabolic disease · 2017
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors.

Eva MoravaCenter for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium. eva.morava@uzleuven.be.
Vera TiemesDepartment of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands.
Christian ThielCenter for Child and Adolescent Medicine, Kinderheilkunde I, University of Heidelberg, Heidelberg, Germany.
Nathalie SetaBiochimie Métabolique Hôpital Bichat-Claude Bernard, Paris, France.
Pascale de LonlayReference Center of Metabolism, Necker-Enfants Malades Hospital, APHP, Imagine Institute, University Paris-Descartes, Paris, France.
Hans de KlerkDepartment of Pediatrics, Erasmus MC - University Medical Center Rotterdam, Emma Hospital, Rotterdam, The Netherlands.
Margot MulderDepartment of Pediatrics, Free University Amsterdam, Amsterdam, The Netherlands.
Estela Rubio-GozalboDepartment of Pediatrics and Laboratory Genetic Metabolic Diseases, University of Maastricht, Maastricht, The Netherlands.
Gepke VisserWilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Peter van HasseltWilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Dafne D G HorovitzMedical Genetics Service, Porto Alegre, RS, Brazil.
Carolina Fischinger Moura de SouzaMedical Genetics Service, Porto Alegre, RS, Brazil.
Ida V D SchwartzMedical Genetics Service, Porto Alegre, RS, Brazil.
Andrew GreenNational Centre for Medical Genetics, Dublin, Ireland.
Mohammed Al-OwainDepartment of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Graciella UzielUniversity of Milan, Institute of Neurology, Milan, Italy.
Sabine SigaudyDépartement de Génétique Médicale, Hôpital Timone Enfant, Marseille, France.
Brigitte ChabrolNeuropediatrics Unit, Childrens Hospital CHU Timone, Marseille, France.
Franc-Jan van SpronsenDivision of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center of Groningen, University of Groningen, Groningen, The Netherlands.
Martin SteinertSozialpädiatrisches Zentrum, Neuropädiatrie, Klinik für Kinder- und Jugendmedizin, Dortmund, Germany.
Eleni KominiKinderklinik Villingen, Schwarzwald-Baar-Klinikum, Villingen, Germany.
Donald WurmDepartment of Pediatrics, Klinikum Saarbrücken, Saarbrücken, Germany.
Andrea BevotDepartment of Pediatric Neurology and Developmental Medicine, Universal Children's Hospital Tübingen, Tübingen, Germany.
Addelkarim AyadiBiochimie Métabolique Hôpital Bichat-Claude Bernard, Paris, France.
Karin HuijbenTranslational Metabolic Laboratory, Department Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Marli DercksenCentre for Human Metabolomics, North-West University, Potchefstroom, South Africa.
Peter WittersCenter for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
Jaak JaekenCenter for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
Gert MatthijsLaboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, Leuven, Belgium.
Dirk J LefeberTranslational Metabolic Laboratory, Department Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Ron A WeversTranslational Metabolic Laboratory, Department Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands. ron.wevers@radboudumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID27498540

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.