Evidence map›Paper›PMID 36696008›Full record

ReviewActa neurologica Belgica2023

Novel mutation in KIF5A gene associated with hereditary motor and sensory neuropathy and cognitive impairment: a case report and literature review.

Uichan Hong, Jinsik Lee, Seohee Choi, Woori Jang, Soonwook Kwon

Abstract readReviewCase ReportsLetter
PubMed Publisher
In one paragraph

Review in Acta neurologica Belgica, 2023. 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
0.3field-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, 2 citations in OpenAlex.

  1. Review
  2. Research progress of kinesin family in neurological diseases.Frontiers in cellular neuroscience · 2025
    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

5 authors at 2 institutions in 1 country.

Uichan HongDepartment of Neurology, Inha University Hospital, 27 Inhang-Ro, Jung-Gu, Incheon, 22332, Korea.
Jinsik LeeDepartment of Neurology, Inha University Hospital, 27 Inhang-Ro, Jung-Gu, Incheon, 22332, Korea.
Seohee ChoiDepartment of Neurology, Inha University Hospital, 27 Inhang-Ro, Jung-Gu, Incheon, 22332, Korea.
Woori JangDepartment of Laboratory Medicine, College of Medicine, Inha University, Incheon, Korea.
Soonwook KwonDepartment of Neurology, Inha University Hospital, 27 Inhang-Ro, Jung-Gu, Incheon, 22332, Korea. ksw_ever@naver.com.ORCID 0000-0002-5578-7571
Inha University Hospital · KRInha University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Charcot-Marie-Tooth DiseaseCognitive DysfunctionHereditary Sensory and Motor NeuropathyHumansKinesinsMutationKIF5A protein, humanKinesins

Identifiers

PMID36696008
OpenAlexW4317935555

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.