Evidence map›Paper›PMID 34185135›Full record

ArticlePediatric nephrology (Berlin, Germany)2021

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers.

Neslihan Günay, Ayşe Seda Pınarbaşı, Muhammet Ensar Doğan, Sibel Yel, Aynur Gencer Balaban, İsmail Dursun, Ahmet Eken, Hülya Akgün, Munis Dündar, Muammer Hakan Poyrazoğlu

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2021. 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
0.1field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

10 authors at 1 institution in 1 country.

Neslihan GünayDepartment of Pediatric Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey.
Ayşe Seda PınarbaşıDepartment of Pediatric Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey.
Muhammet Ensar DoğanDepartment of Medical Genetics, Erciyes University Medical Faculty, Kayseri, Turkey.
Sibel YelDepartment of Pediatric Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey.
Aynur Gencer BalabanDepartment of Pediatric Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey.
İsmail DursunDepartment of Pediatric Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey. idursun@erciyes.edu.tr.ORCID https://orcid.org/0000-0002-0191-4344
Ahmet EkenDepartment of Medical Biology, Erciyes University Medical Faculty, Kayseri, Turkey.
Hülya AkgünDepartment of Pathology, Erciyes University Medical Faculty, Kayseri, Turkey.
Munis DündarDepartment of Medical Genetics, Erciyes University Medical Faculty, Kayseri, Turkey.
Muammer Hakan PoyrazoğluDepartment of Pediatric Nephrology, Erciyes University Medical Faculty, Kayseri, Turkey.
Erciyes University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DGKEDiacylglycerol kinase epsilonHemolytic uremic syndromeMembranoproliferative glomerulonephritisNephrotic syndromePediatric

Identifiers

PMID34185135
OpenAlexW3175694896

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.