Evidence map›Paper›PMID 30349702›Full record

ArticleClinical case reports2018

Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a

Valérie Leclercq, Valérie Benoit, Damien Lederer, Melanie Delaunoy, Marcela Ruiz, Claire de Halleux, Olivier Robaux, Catherine Wanty, Isabelle Maystadt

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

Article in Clinical case reports, 2018. 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
0.2field-weighted citation impact, top 37% 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, 6 citations in OpenAlex.

  1. Review
  2. Journal of dental research · 2022
    Article
  3. Article
  4. 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

9 authors at 3 institutions in 1 country.

Valérie LeclercqCentre de Génétique Humaine Institut de Pathologie et de Génétique Gosselies Belgium.ORCID 0000-0003-1240-8225
Valérie BenoitCentre de Génétique Humaine Institut de Pathologie et de Génétique Gosselies Belgium.
Damien LedererCentre de Génétique Humaine Institut de Pathologie et de Génétique Gosselies Belgium.
Melanie DelaunoyCentre de Génétique Humaine ULB Hôpital Erasme Bruxelles Belgium.
Marcela RuizDépartement de Pédiatrie Grand Hôpital de Charleroi Charleroi Belgium.
Claire de HalleuxDépartement de Pédiatrie Grand Hôpital de Charleroi Charleroi Belgium.
Olivier RobauxDépartement de Pédiatrie Grand Hôpital de Charleroi Charleroi Belgium.
Catherine WantyDépartement de Pédiatrie Grand Hôpital de Charleroi Charleroi Belgium.
Isabelle MaystadtCentre de Génétique Humaine Institut de Pathologie et de Génétique Gosselies Belgium.
Grand Charleroi Hospital · BEInstitute of Pathology and Genetics · BEErasmus Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline loss-of-function

Indexed as

Albright's hereditary osteodystrophyGNAS mutationinactivating PTH/PTHrP signaling disorderspseudohypoparathyroidismsevere phenotype

Identifiers

PMID30349702
PMCPMC6186887
OpenAlexW2886001966

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.