Evidence map›Paper›PMID 30962759›Full record

ArticleYonago acta medica2019

Recurrent Erythema Nodosum in a Child with a

Tetsuya Okazaki, Yoshiaki Saito, Kazunari Sugita, Kanae Nosaka, Koyo Ohno, Yumie Hiraoka, Noriko Kasagi, Mitsutaka Ebiki, Satoshi Narai, Yuki Kawashima and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Yonago acta medica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

16 authors at 4 institutions in 3 countries.

Tetsuya OkazakiDivision of Child Neurology, Department of Brain and Neurosciences, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Yoshiaki SaitoDivision of Child Neurology, Department of Brain and Neurosciences, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Kazunari Sugita‡Division of Dermatology, Department of Medicine of Sensory and Motor Organs, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Kanae Nosaka§Division of Organ Pathology, Department of Pathology, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Koyo OhnoDivision of Child Neurology, Department of Brain and Neurosciences, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Yumie Hiraoka†Department of Clinical Genetics, Tottori University Hospital, Yonago 683-8504, Japan.
Noriko Kasagi†Department of Clinical Genetics, Tottori University Hospital, Yonago 683-8504, Japan.
Mitsutaka Ebiki||The Development of Innovative Future Medical Treatment, Graduate School of Medical Sciences, Tottori University, Yonago 683-8504, Japan.
Satoshi Narai*Division of Pediatrics and Perinatology, Department of Multidisciplinary Internal Medicine, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Yuki Kawashima*Division of Pediatrics and Perinatology, Department of Multidisciplinary Internal Medicine, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Shuichi Takano††Division of Surgical Oncology, Department of Surgery, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Masachika Kai‡‡Division of Technical Department, Tottori University, Yonago 683-8503, Japan.
Kaori Adachi§§Research Initiative Center, Organization for Research Initiative and Promotion, Tottori University, Yonago 683-8503, Japan.
Osamu Yamamoto‡Division of Dermatology, Department of Medicine of Sensory and Motor Organs, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Eiji Nanba†Department of Clinical Genetics, Tottori University Hospital, Yonago 683-8504, Japan.
Yoshihiro MaegakiDivision of Child Neurology, Department of Brain and Neurosciences, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504, Japan.
Tottori University · JPTottori University Hospital · JPGlobal Strategy Group · USInstitute Of Perinatology Obstetrics And Gynaecology · AM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the case of a 6-year-old male who developed recurrent erythema nodosum (EN) at the age of 3 years. The patient exhibited hypertelorism, low-set ears, micrognathia, moderate intellectual disability, thin long fingers, loose anagen hair, and prominent palmoplantar wrinkles. A heterozygous single nucleotide variant in the

Indexed as

erythema nodosumloose anagen hairnext-generation sequencingNoonan syndromeSHOC2

Identifiers

PMID30962759
PMCPMC6437419
OpenAlexW2924335298

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.