Evidence map›Paper›PMID 35729459›Full record

ArticleWiener medizinische Wochenschrift (1946)2023

Anti-MDA5 antibody-positive dermatomyositis with mild encephalopathy with reversible splenial lesion: a possible rare association?

Khadija Saghir, Mohammed Chraa, Najib Kissani, Hajar Joulal, Lamiaa Essaadouni, Nissrine Louhab

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

Article in Wiener medizinische Wochenschrift (1946), 2023. 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
0.2field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Khadija SaghirNeuroscience Research Laboratory, Marrakech Medical School, Cadi Ayyad University, Marrakech, Morocco. saghirkhadija91@gmail.com.ORCID http://orcid.org/0000-0003-3619-2262
Mohammed ChraaNeuroscience Research Laboratory, Marrakech Medical School, Cadi Ayyad University, Marrakech, Morocco.
Najib KissaniNeuroscience Research Laboratory, Marrakech Medical School, Cadi Ayyad University, Marrakech, Morocco.
Hajar JoulalNeuroscience Research Laboratory, Marrakech Medical School, Cadi Ayyad University, Marrakech, Morocco.
Lamiaa EssaadouniNeuroscience Research Laboratory, Marrakech Medical School, Cadi Ayyad University, Marrakech, Morocco.
Nissrine LouhabNeuroscience Research Laboratory, Marrakech Medical School, Cadi Ayyad University, Marrakech, Morocco.
Cadi Ayyad University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Central nervous system (CNS) involvement in dermatomyositis (DM) is seldom observed. However, there are very rare case reports of CNS involvement with juvenile dermatomyositis. Encephalopathy in DM may occur for a number of reasons, such as cerebral vasculitis and hypoperfusion/hypertensive encephalopathy, but mostly as a consequence of immunosuppressant treatment. We report here for the first time the case of a patient with two rare diseases, namely anti-MDA5 antibody-positive dermatomyositis and mild encephalopathy with reversible splenial lesion (MERS).

Indexed as

Brain DiseasesDermatomyositisEncephalitisCorpus CallosumHumansCorpus callosumEncephalitisInterleukinsMagnetic resonance imagingMyopathy

Identifiers

PMID35729459
PMCPMC9211780
OpenAlexW4283266776

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.