Evidence map›Paper›PMID 30863911›Full record

ArticlePediatric nephrology (Berlin, Germany)2019

Nephrotic syndrome and mitochondrial disorders: answers.

Julie Bernardor, Camille Faudeux, Anabelle Chaussenot, Corinne Antignac, Alice Goldenberg, Marie Claire Gubler, Nicole Wagner, Etienne Bérard

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2019. 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
–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

1 citing paper in PubMed.

  1. Every Beat You Take-The Wilms' Tumor Suppressor WT1 and the Heart.International journal of molecular sciences · 2021
    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

8 authors.

Julie BernardorUnité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
Camille FaudeuxUnité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
Anabelle ChaussenotService de génétique médicale, CHU de Nice - Hôpital Archet 2, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
Corinne AntignacLaboratoire des maladies rénales héréditaires 1 - INSERM UMR S1163, Institut Imagine, 24 boulevard du Montparnasse, 75015, Paris, France.
Alice GoldenbergUnité de génétique clinique - CHU de Rouen, 1 Rue de Germont, 76031, Rouen Cedex, France.
Marie Claire GublerLaboratoire des maladies rénales héréditaires 1 - INSERM UMR S1163, Institut Imagine, 24 boulevard du Montparnasse, 75015, Paris, France.
Nicole WagnerCNRS, INSERM, iBV, Université Côte d'Azur, 06107, Nice, France.
Etienne BérardUnité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France. berard.e@chu-nice.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdolescentBiopsyCardiomyopathy, DilatedChildChild, PreschoolDeafnessGenetic TestingHigh-Throughput Nucleotide SequencingHumansInfantInfant, NewbornIntronsKidneyLongitudinal StudiesMaleMembrane ProteinsMembrane ProteinsnephrinCardiomyopathyChildCongenital nephrotic syndrome (CNF)Mitochondrial disorderNPHS1 mutation

Identifiers

PMID30863911

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.