Evidence map›Paper›PMID 30023306›Full record

ArticleMolecular genetics and metabolism reports2018

Phenotypic spectrum of maternally inherited Leigh Syndrome associated with the m.8993T>G variant.

Andrea Gropman, Anne Chiaramello

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2018. 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

2 authors.

Andrea GropmanChildren's National Medical Center, Division of Neurogenetics and Developmental Pediatrics, Washington, DC 20010, USA.
Anne ChiaramelloDepartment of Anatomy and Regenerative Biology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA.

Funding

Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI LIMPEROPOULOS, CATHERINE · 2016 to 2020
$5.9M
A Pharmaco-Epigenomic Intervention for the Mitochondrial Disorder MELASR21NS085282 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI CHIARAMELLO, ANNE ELIANE · 2015 to 2016
$809k
NICHD NIH HHS U54 HD090257NINDS NIH HHS R21 NS085282
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Hydrocephalus ex vacuoInfantile spasmsLeigh Syndromem.8993T>G variantPhenotypic variability

Identifiers

PMID30023306
PMCPMC6047217

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.