Evidence map›Paper›PMID 31448769›Full record

ArticleJournal of clinical research in pediatric endocrinology2020

Hypoprolactinemia as a Clue to Diagnosis of Mild Central Hypothyroidism due to

Anastasios Papadimitriou, Anna Papadopoulou, Kleanthis Kleanthous, Dimitrios T. Papadimitriou, Vassiliki Papaevangelou

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

Article in Journal of clinical research in pediatric endocrinology, 2020. 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 43% 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. Isolated hypoprolactinemia: The rarest of the rare?Reviews in endocrine & metabolic disorders · 2024
    Review
  2. The molecular basis of hypoprolactinaemia.Reviews in endocrine & metabolic disorders · 2024
    Review
  3. 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

5 authors at 1 institution in 1 country.

Anastasios PapadimitriouNational and Kapodistrian University of Athens, “Attikon” University Hospital, Third Department of Pediatrics, Athens, GreeceORCID 0000-0003-4130-2155
Anna PapadopoulouNational and Kapodistrian University of Athens, “Attikon” University Hospital, Third Department of Pediatrics, Athens, GreeceORCID 0000-0001-8806-6255
Kleanthis KleanthousNational and Kapodistrian University of Athens, “Attikon” University Hospital, Third Department of Pediatrics, Athens, GreeceORCID 0000-0001-8707-4667
Dimitrios T. PapadimitriouNational and Kapodistrian University of Athens, “Attikon” University Hospital, Third Department of Pediatrics, Athens, GreeceORCID 0000-0002-6083-3560
Vassiliki PapaevangelouNational and Kapodistrian University of Athens, “Attikon” University Hospital, Third Department of Pediatrics, Athens, GreeceORCID 0000-0001-6075-3002
National and Kapodistrian University of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loss-of-function mutations of

Indexed as

AdolescentHumansHypothyroidismImmunoglobulinsMaleMembrane ProteinsProlactinIGSF1 protein, humanImmunoglobulinsMembrane ProteinsProlactinCentral hypothyroidismhypoprolactinemiaIGSF1

Identifiers

PMID31448769
PMCPMC7291406
OpenAlexW2971152908

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.