Evidence map›Paper›PMID 39135905›Full record

ArticleInternational journal of endocrinology2024

Expanding the Phenotype of Congenital Glucocorticoid Deficiency: An Iranian Patient with Cholestasis due to Pathogenic Variants in the

Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi, Afagh Hassanzadeh Rad, Reza Bayat, Bahareh Rabbani, Nejat Mahdieh

Abstract read
In one paragraph

Article in International journal of endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Shohreh MaleknejadPediatric Diseases Research Center Guilan University of Medical Sciences, Rasht, Iran.ORCID https://orcid.org/0000-0002-3865-5753
Setila DaliliPediatric Diseases Research Center Guilan University of Medical Sciences, Rasht, Iran.ORCID https://orcid.org/0000-0001-9591-0821
Ameneh SharifiGrowth and Development Research Center Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0001-9893-2532
Afagh Hassanzadeh RadPediatric Diseases Research Center Guilan University of Medical Sciences, Rasht, Iran.ORCID https://orcid.org/0000-0001-6980-8866
Reza BayatPediatric Diseases Research Center Guilan University of Medical Sciences, Rasht, Iran.ORCID https://orcid.org/0000-0002-8956-5205
Bahareh RabbaniGrowth and Development Research Center Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0003-1083-1660
Nejat MahdiehCardiogenetic Research Center Rajaie Cardiovascular Medical and Research Institute Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-8614-1538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial glucocorticoid deficiency is caused by variants in the

Identifiers

PMID39135905
PMCPMC11319056

What Socratic 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 Socratic graph.