Evidence map›Paper›PMID 36101819›Full record

ArticleJIMD reports2022

Glycogen storage disease type 1a in the Ohio Amish.

Ethan M Scott, Olivia K Wenger, Elizabeth Robinson, Kristina Colling, Miraides F Brown, Jennifer Hershberger, Kadakkal Radhakrishnan

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in JIMD reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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.

Ethan M ScottNew Leaf Center Clinic for Special Children Ohio USA.ORCID https://orcid.org/0000-0002-2129-9422
Olivia K WengerNew Leaf Center Clinic for Special Children Ohio USA.
Elizabeth RobinsonDepartment of Pediatric Gastroenterology, Hepatology, and Nutrition Cleveland Clinic Foundation Cleveland Ohio USA.
Kristina CollingDepartment of Pediatric Gastroenterology, Hepatology, and Nutrition Cleveland Clinic Foundation Cleveland Ohio USA.
Miraides F BrownAkron Children's Hospital Rebecca D Considine Research Institute Akron Ohio USA.
Jennifer HershbergerNew Leaf Center Clinic for Special Children Ohio USA.
Kadakkal RadhakrishnanDepartment of Pediatric Gastroenterology, Hepatology, and Nutrition Cleveland Clinic Foundation Cleveland Ohio USA.
Cleveland Clinic · USClinic for Special Children · USAkron Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycogen storage disease type 1a (GSD1a) is an inborn error of glucose metabolism characterized by fasting hypoglycemia, hepatomegaly, and growth failure. Late complications include nephropathy and hepatic adenomas. We conducted a retrospective observational study on a cohort of Amish patients with GSD1a. A total of 15 patients cared for at a single center, with a median age of 9.9 years (range 0.25-24 years) were included. All patients shared the same founder variant in

Indexed as

gross motor delayhepatomegalyhypertriglyceridemiahypoglycemiaoral aversionquality of life

Identifiers

PMID36101819
PMCPMC9458600
OpenAlexW4283215094

What OpenQuestion 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 OpenQuestion graph.