Evidence map›Paper›PMID 33344924›Full record

ArticleEpilepsy & behavior reports2020

Successful treatment of drug-resistant status epilepticus in an adult patient with Mowat-Wilson syndrome: A case report.

Yasunobu Nosaki, Ken Ohyama, Maki Watanabe, Takamasa Yokoi, Yosuke Kobayashi, Mie Inaba, Nobuaki Wakamatsu, Katsushige Iwai

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

Article in Epilepsy & behavior reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Electro-clinical features of Mowat-Wilson syndrome: A retrospective study of 31 children in mainland China.Epileptic disorders : international epilepsy journal with videotape · 2026
    Article
  3. 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 at 3 institutions in 1 country.

Yasunobu NosakiDepartment of Neurology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Ken OhyamaDepartment of Neurology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Maki WatanabeDepartment of Neurology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Takamasa YokoiDepartment of Neurology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Yosuke KobayashiDepartment of Neurology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Mie InabaDepartment of Pediatrics, Aichi Developmental Disability Center Central Hospital, Kasugai, Japan.
Nobuaki WakamatsuDepartment of Neurology, Takamatsu Municipal Hospital, Takamatsu, Japan.
Katsushige IwaiDepartment of Neurology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Toyohashi Municipal Hospital · JPAichi Developmental Disability Center · JPNational Hospital Organization Takamatsu Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mowat-Wilson syndrome (MWS) is a rare genetic disorder characterized by intellectual disability, distinctive facial features, epilepsy, and multiple anomalies caused by heterozygous loss-of-function mutations in the zinc finger E-box-binding homeobox-2 gene (

Indexed as

Anti-seizure drugsConvulsive status epilepticusDrug-resistantMagnetic resonance imagingMowat-Wilson syndromeZEB2

Identifiers

PMID33344924
PMCPMC7736901
OpenAlexW3106666461

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.