Evidence map›Paper›PMID 34307994›Full record

ArticleKidney international reports2021

Antenatal Membranous Nephropathy and Type 2 (Axonal) Charcot-Marie-Tooth With Mutations in the Metallo-Membrane Endopeptidase Gene: A Call for Family Screening and Pharmacovigilance.

Joëlle L Nortier, Gauthier Remiche, Paul Delrée, Jeroen Nauta, Nicolette C Notermans, Marina Vivarelli, Daria Diodato, Guilhem Solé, Hanna Debiec, Pierre Ronco

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

Article in Kidney international reports, 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
–field-weighted citation impact, top 94% 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, 0 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 9 institutions in 4 countries.

Joëlle L NortierNephrology Department, CHU Brugmann, Université libre de Bruxelles, Brussels, Belgium.
Gauthier RemicheNeurology Department, Centre de Référence Neuromusculaire Erasme-HUDERF, Hôpital Erasme, Université libre de Bruxelles, Brussels, Belgium.
Paul DelréePathology Department, Institute of Pathology and Genetics, Gosselies, Belgium.
Jeroen NautaDepartment of Pediatric Nephrology, Erasmus MC, Sophia Childrens Hospital, Rotterdam, The Netherlands.
Nicolette C NotermansDepartment of Neurology, University Medical Center, Utrecht, The Netherlands.
Marina VivarelliU.O. Nefrologia e Dialisi, Children's Hospital Bambino Gesù, IRCCS, Roma, Italy.
Daria DiodatoNeuromuscular and Neurodegenerative Diseases Unit, Children Research, Children's Hospital Bambino Gesù, IRCCS, Roma, Italy.
Guilhem SoléCentre de référence des maladies neuromusculaires AOC, Pellegrin Hospital, Bordeaux, France.
Hanna DebiecSorbonne Université, Inserm UMR_S1155, Tenon Hospital, Paris, France.
Pierre RoncoSorbonne Université, Inserm UMR_S1155, Tenon Hospital, Paris, France.
Bambino Gesù Children's Hospital · ITCentre Hospitalier du Mans · FRCentre Hospitalier Universitaire Brugmann · BEErasmus Hospital · BEErasmus MC - Sophia Children’s Hospital · NLHôpital Pellegrin · FRHôpital Tenon · FRInstitute of Pathology and Genetics · BEUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

congenital nephropathymaternofetal allo-immunizationmembranous nephropathyMME geneneprilysinneutral endopeptidaseperipheral neuropathy

Identifiers

PMID34307994
PMCPMC8258500
OpenAlexW3161729978

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.