Evidence map›Paper›PMID 36581364›Full record

ArticleBMJ case reports2022

Growth hormone deficiency in a case of septo-optic-dysplasia due to

Valentina Gasco, Patrizia Matarazzo, Luisa De Sanctis, Ezio Ghigo

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

Article in BMJ case 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
0.4field-weighted citation impact, top 34% 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, 3 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

4 authors at 1 institution in 1 country.

Valentina GascoDivision of Endocrinology, Diabetes and Metabolism, Department of Medical Science, University of Turin, Turin, Piedmont, Italy valentina.gasco@unito.it.
Patrizia MatarazzoDepartment of Public Health and Pediatrics, University of Turin, Turin, Piedmont, Italy.
Luisa De SanctisDepartment of Public Health and Pediatrics, University of Turin, Turin, Piedmont, Italy.
Ezio GhigoDivision of Endocrinology, Diabetes and Metabolism, Department of Medical Science, University of Turin, Turin, Piedmont, Italy.
University of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene mutations encoding transcription factors, including

Indexed as

Dwarfism, PituitaryHuman Growth HormoneHypopituitarismSepto-Optic DysplasiaChildGrowth HormoneHumansMutationPituitary GlandSOXB1 Transcription FactorsGrowth HormoneHuman Growth HormoneSOX2 protein, humanSOXB1 Transcription FactorsCongenital disordersPituitary disorders

Identifiers

PMID36581364
PMCPMC9806035
OpenAlexW4313267818

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.