Evidence map›Paper›PMID 26373950›Full record

ArticleJournal of inherited metabolic disease2016

Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype.

Ann Bowron, Julie Honeychurch, Maggie Williams, Beverley Tsai-Goodman, Nicol Clayton, Lucy Jones, Graham J Shortland, Shakeel A Qureshi, Simon J R Heales, Colin G Steward

Abstract readPublished Erratum
PubMed Full text at PMC 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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Ann BowronDepartment of Clinical Biochemistry, University Hospitals Bristol NHS Trust, Bristol, BS2 8HW, UK. ann.bowron@bristol.ac.uk.
Julie HoneychurchBristol Genetics Laboratory, North Bristol NHS Trust, Bristol, BS10 5NB, UK.
Maggie WilliamsBristol Genetics Laboratory, North Bristol NHS Trust, Bristol, BS10 5NB, UK.
Beverley Tsai-GoodmanNHS Barth Syndrome Service, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK.
Nicol ClaytonNHS Barth Syndrome Service, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK.
Lucy JonesNHS Barth Syndrome Service, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK.
Graham J ShortlandDepartment of Metabolic Disease, University Hospitals Wales, Cardiff, CF14 4XW, UK.
Shakeel A QureshiDepartment of Paediatric Cardiology, Evelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SE1 7EH, UK.
Simon J R HealesDepartment of Chemical Pathology, Great Ormond Street Hospital NHS Foundation Trust, London, WC1N 3JH, UK.
Colin G StewardNHS Barth Syndrome Service, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID26373950
PMCPMC4969951

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.