Evidence map›Paper›PMID 38469099›Full record

ArticleMolecular genetics and metabolism reports2024

Critical sample collection delayed? Urine organic acid analysis can still save the day! A new case of HMG-CoA synthase deficiency.

Monika Williams, Iskren Menkovic, Pamela Reitnauer, Eileen Gilbert, Dwight Koeberl, Sarah P Young, Ashlee R Stiles

Open access · goldAbstract readCase Reports
In one paragraph

Article in Molecular genetics and metabolism reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 20% of its field
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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Monika WilliamsDepartment of Pediatrics, Division of Pediatric Genetics and Metabolism, UNC, Chapel Hill, NC, USA.
Iskren MenkovicBiochemical Genetics Laboratory, Duke University Health System, Durham, NC, USA.
Pamela ReitnauerPediatric Teaching Program & Pediatric Medical Genetics, Cone Health, Greensboro, NC, USA.
Eileen GilbertBiochemical Genetics Laboratory, Duke University Health System, Durham, NC, USA.
Dwight KoeberlBiochemical Genetics Laboratory, Duke University Health System, Durham, NC, USA.
Sarah P YoungBiochemical Genetics Laboratory, Duke University Health System, Durham, NC, USA.
Ashlee R StilesBiochemical Genetics Laboratory, Duke University Health System, Durham, NC, USA.
Duke University Health System · USCone Health · USUniversity of North Carolina Health Care · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) synthase (mHS) deficiency is an autosomal recessive disorder of ketone body synthesis caused by biallelic pathogenic variants in

Indexed as

4-hydroxy-6-methyl-2-pyroneHMG-CoA synthase deficiencyMitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiencyNon-ketotic hypoglycemiaUrine organic acids

Identifiers

PMID38469099
PMCPMC10926198
OpenAlexW4391460188

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.