Evidence map›Paper›PMID 34514047›Full record

ArticleMovement disorders clinical practice2021

Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life.

Jennifer Friedman, Sara Lucas-Del-Pozo, David Moreno-Martinez, Maria Camprodon-Gomez, Daniel Moreno-Martinez, Jorge Hernandez-Vara, Manju A Kurian

Abstract readEditorial
In one paragraph

Article in Movement disorders clinical practice, 2021. 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

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

7 authors.

Jennifer FriedmanDepartment of Neurosciences and Pediatrics University of California Los Angeles California USA.
Sara Lucas-Del-PozoNeurodegenerative Diseases Research Group, Vall Hebron Research Institute Vall Hebron University Hospital Barcelona Spain.
David Moreno-MartinezLysosomal Storage Disorders Unit Royal Free Hospital National Health Service Foundation Trust and University College London London United Kingdom.
Maria Camprodon-GomezRare Diseases and Inborn Errors of Metabolism Unit Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona Barcelona Spain.
Daniel Moreno-MartinezNeuroradiology Department Vall Hebron University Hospital Barcelona Spain.
Jorge Hernandez-VaraNeurodegenerative Diseases Research Group, Vall Hebron Research Institute Vall Hebron University Hospital Barcelona Spain.
Manju A KurianDevelopmental Neurosciences, Zayed Centre for Research into Rare Diseases in Children Great Ormond Street Institute of Child Health, UCL London United Kingdom.ORCID https://orcid.org/0000-0003-3529-5075

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

cerebral palsydevelopmental delayGalactosemia

Identifiers

PMID34514047
PMCPMC8414503

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.