Evidence map›Paper›PMID 29537382›Full record

ArticleJournal of clinical research in pediatric endocrinology2018

A Novel Variant c.97C>T of the Growth Hormone Releasing Hormone Receptor Gene Causes Isolated Growth Hormone Deficiency Type Ib

Assimina Galli-Tsinopoulou, Eleni P. Kotanidou, Aggeliki N. Kleisarchaki, Rivka Kauli, Zvi Laron

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

Article in Journal of clinical research in pediatric endocrinology, 2018. 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
0.5field-weighted citation impact, top 33% 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. Article
  2. Article
  3. An update on the diagnosis of growth hormone deficiency.Discoveries (Craiova, Romania) · 2018
    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

5 authors at 4 institutions in 2 countries.

Assimina Galli-TsinopoulouAristotle University of Thessaloniki Faculty of Health Sciences, School of Medicine, Papageorgiou General Hospital, 4
Eleni P. KotanidouAristotle University of Thessaloniki Faculty of Health Sciences, School of Medicine, Papageorgiou General Hospital, 4
Aggeliki N. KleisarchakiAristotle University of Thessaloniki Faculty of Health Sciences, School of Medicine, Papageorgiou General Hospital, 4
Rivka KauliTel Aviv University Sackler Faculty of Medicine, Schneider Children’s Medical Center of Israel, Clinic of Endocrinology and Diabetes Research, Tel Aviv, Israel
Zvi LaronTel Aviv University Sackler Faculty of Medicine, Schneider Children’s Medical Center of Israel, Clinic of Endocrinology and Diabetes Research, Tel Aviv, Israel
Aristotle University of Thessaloniki · GRPapageorgiou General Hospital · GRSchneider Children's Medical Center · ILTel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital isolated growth hormone deficiency (IGHD) type 1b is an autosomal recessive genetic condition caused by mutations of growth hormone (GH)-1 or the growth hormone releasing hormone receptor (

Indexed as

Codon, NonsenseDwarfismFemaleHumansInfantPituitary DiseasesReceptors, NeuropeptideReceptors, Pituitary Hormone-Regulating HormoneCodon, NonsenseReceptors, NeuropeptideReceptors, Pituitary Hormone-Regulating Hormonesomatotropin releasing hormone receptorCongenital isolated growth hormone deficiencyfailure to thrivegrowth hormone releasing hormone receptorshort stature

Identifiers

PMID29537382
PMCPMC6083476
OpenAlexW2790891131

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.