Evidence map›Paper›PMID 28589169›Full record

ArticleAnnals of clinical and translational neurology2017

Partial duplication of

Naoko Saito Sato, Risa Maekawa, Hiroyuki Ishiura, Jun Mitsui, Hiroya Naruse, Shin-Ichi Tokushige, Kazuma Sugie, Genshu Tate, Jun Shimizu, Jun Goto and 2 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Differences of sex development.Nature reviews. Disease primers · 2025
    Review
  2. Review
  3. New observations on minifascicular neuropathy with sex-dependent gonadal dysgenesis: a case series with nerve ultrasound assessment.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
    Observational
  4. Review
  5. Peripheral glia diversity.Journal of anatomy · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. A novel, homozygous mutation inInternational journal of pediatric endocrinology · 2018
    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

12 authors at 5 institutions in 1 country.

Naoko Saito SatoDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Risa MaekawaDepartment of Neurology Tokyo Teishin Hospital Tokyo Japan.
Hiroyuki IshiuraDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Jun MitsuiDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Hiroya NaruseDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Shin-Ichi TokushigeDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Kazuma SugieDepartment of Neurology Nara Medical University Nara Japan.
Genshu TateDepartment of Surgical Pathology Showa University Fujigaoka Hospital Kanagawa Japan.
Jun ShimizuDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Jun GotoDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Shoji TsujiDepartment of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Yasushi ShiioDepartment of Neurology Tokyo Teishin Hospital Tokyo Japan.
The University of Tokyo · JPTokyo Teishin Hospital · JPMita Hospital · JPNara Medical University · JPShowa University Fujigaoka Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Minifascicular neuropathy (MN) is an extremely rare developmental malformation in which peripheral nerves are composed of many small fascicles. Only one patient with MN with 46XY gonadal dysgenesis (GD) was found to carry a mutation affecting the start codon in

Identifiers

PMID28589169
PMCPMC5454394
OpenAlexW2620078313

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.