Evidence map›Paper›PMID 25687635›Full record

ArticleThe Journal of pediatrics2015

Premature pubarche in children with Pompe disease.

Queenie K-G Tan, David W Stockton, Eniko Pivnick, Asim F Choudhri, Stacy Hines-Dowell, Loren D M Pena, Melissa A Deimling, Michael S Freemark, Priya S Kishnani

Open access · greenAbstract readMulticenter Study
PubMed Full text at PMC Publisher
In one paragraph

Article in The Journal of pediatrics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Precocious puberty in patients with Pompe disease.Frontiers in endocrinology · 2023
    Article
  2. Article
  3. Advances in imaging of brain abnormalities in neuromuscular disease.Therapeutic advances in neurological disorders · 2019
    Review
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

9 authors at 4 institutions in 1 country.

Queenie K-G TanDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC.
David W StocktonDivision of Genetic and Metabolic Disorders, Departments of Pediatrics and Internal Medicine, Wayne State University and Children's Hospital of Michigan, Detroit, MI.
Eniko PivnickDivision of Medical Genetics, Department of Pediatrics, University of Tennessee; Le Bonheur Children's Hospital, Memphis, TN.
Asim F ChoudhriDepartments of Radiology, Ophthalmology, and Neurosurgery, University of Tennessee Health Science Center; Le Bonheur Neuroscience Institute, Le Bonheur Children's Hospital, Memphis, TN.
Stacy Hines-DowellDivision of Medical Genetics, Department of Pediatrics, University of Tennessee; Le Bonheur Children's Hospital, Memphis, TN.
Loren D M PenaDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC.
Melissa A DeimlingDivision of Primary Care, Department of Pediatrics, Duke University Medical Center, Durham, NC.
Michael S FreemarkDivision of Endocrinology, Department of Pediatrics, Duke University Medical Center, Durham, NC.
Priya S KishnaniDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC. Electronic address: priya.kishnani@duke.edu.
Duke Medical Center · USUniversity of Tennessee at Knoxville · USChildren's Hospital of Michigan · USLe Bonheur Children's Hospital · US

Funding

Training & EducationU54NS065768 · NINDS · UNIVERSITY OF MINNESOTA · PI WHITLEY, CHESTER B. · 2009 to 2024
$17.7M
NINDS NIH HHS U54 NS065768NINDS NIH HHS U54NS065768
6 · The paper itself

Abstract

Pompe disease (PD), or glycogen storage disease type II, results from deficiency of acid α-glucosidase. Patients with infantile-onset PD die by early childhood if untreated. Patient survival has improved with enzyme replacement therapy. We report a case series of 8 patients with infantile-onset PD on enzyme replacement therapy with premature pubarche.

Indexed as

PubertySexual DevelopmentChildChild, PreschoolEnzyme Replacement TherapyFemaleFollow-Up StudiesGlycogen Storage Disease Type IIHumansInfantMalePrognosisRetrospective Studies

Identifiers

PMID25687635
PMCPMC10880744
OpenAlexW2062971254

What OpenQuestion holds

Textmetadata
LicenceTDM
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.