Evidence map›Paper›PMID 33454747›Full record

ArticleBrain : a journal of neurology2021

Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.

Rauan Kaiyrzhanov, Saskia Wortmann, Taryn Reid, Mohammadreza Dehghani, Mohammad Yahya Vahidi Mehrjardi, Bader Alhaddad, Matias Wagner, Marcus Deschauer, Isabell Cordts, J Pedro Fernandez-Murray and 8 more

Erratum issuedAbstract readLetterComment
In one paragraph

Article in Brain : a journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  12. Article
  13. Genetic diseases of the Kennedy pathways for membrane synthesis.The Journal of biological chemistry · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Rauan KaiyrzhanovDepartment of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London, UK.
Saskia WortmannInstitute of Human Genetics, Technical University Munich, Munich, Germany.
Taryn ReidDepartment of Pharmacology, Dalhousie University, Halifax, Canada.
Mohammadreza DehghaniMedical Genetics Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Mohammad Yahya Vahidi MehrjardiAbortion Research Centre, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Bader AlhaddadInstitute of Human Genetics, Technical University Munich, Munich, Germany.
Matias WagnerInstitute of Human Genetics, Technical University Munich, Munich, Germany.
Marcus DeschauerDepartment of Neurology, Technical University of Munich, School of Medicine, Munich, Germany.
Isabell CordtsDepartment of Neurology, Technical University of Munich, School of Medicine, Munich, Germany.
J Pedro Fernandez-MurrayDepartment of Pharmacology, Dalhousie University, Halifax, Canada.
Veronika TrefferInstitute of Human Genetics, Technical University Munich, Munich, Germany.
Zahra MetanatProvincial Clinical Genetic Counselling Center, Zahedan University of Medical Sciences Zahedan, Iran.
Alan PitmanGenetics Centre, Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
Henry HouldenDepartment of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London, UK.
Thomas MeitingerInstitute of Human Genetics, Technical University Munich, Munich, Germany.
Christopher CarrollGenetics Centre, Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
Christopher R McMasterDepartment of Pharmacology, Dalhousie University, Halifax, Canada.
Reza MaroofianDepartment of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London, UK.

Funding

Medical Research Council G0601943Medical Research Council MR/S005021/1Medical Research Council MR/S01165X/1Wellcome Trust
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cerebellar AtaxiaPhosphatidylethanolaminesAtaxiaHumansMuscle SpasticityPhosphatidylethanolamines

Identifiers

PMID33454747
PMCPMC8041042

What Socratic 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 Socratic graph.