Evidence map›Paper›PMID 37908565›Full record

ArticleJCEM case reports2023

Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism.

Christine P Burren, Georgina Williams, Edward Coxson, Márta Korbonits

Open access · diamondAbstract readCase Reports
In one paragraph

Article in JCEM case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Can acromegaly be controlled in all cases?Journal of neuroendocrinology · 2026
    Review
  2. Genetics of familial acromegaly and pituitary gigantism.The Journal of clinical endocrinology and metabolism · 2026
    Review
  3. Review
  4. Article
  5. 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

4 authors at 4 institutions in 1 country.

Christine P BurrenDepartment of Paediatric Endocrinology and Diabetes, Bristol Royal Hospital for Children, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol BS1 3NU, UK.ORCID https://orcid.org/0000-0002-3778-2945
Georgina WilliamsDepartment of Paediatric Endocrinology, Noah's Ark Children's Hospital for Wales, Cardiff CF14 4XW, UK.
Edward CoxsonDepartment Paediatrics, Royal United Hospital, Bath BA1 3NG, UK.
Márta KorbonitsCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London EC1M 6BQ, UK.ORCID https://orcid.org/0000-0002-4101-9432
Noah's Ark Children's Hospital for Wales · GBQueen Mary University of London · GBRoyal United Hospital · GBUniversity Hospitals Bristol NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked acrogigantism (X-LAG) is characterized by extreme tall stature from early childhood resulting from duplication of the

Indexed as

gigantismgrowth hormone receptor antagonistpegvisomantX-linked acrogigantism

Identifiers

PMID37908565
PMCPMC10580488
OpenAlexW4381596817

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.