Evidence map›Paper›PMID 31122137›Full record

ArticlePrion2019

Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia.

Runcheng He, Yacen Hu, Lingyan Yao, Yun Tian, Yafang Zhou, Fang Yi, Lin Zhou, Hongwei Xu, Qiying Sun

Open access · goldAbstract read
In one paragraph

Article in Prion, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Prion Mutations in Republic of Republic of Korea, China, and Japan.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Article
  8. 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

9 authors at 2 institutions in 1 country.

Runcheng Hea Department of Neurology , Xiangya Hospital, Central South University , Changsha , Hunan , China.
Yacen Hub National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Lingyan Yaob National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Yun Tianb National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Yafang Zhoub National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Fang Yib National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Lin Zhoub National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Hongwei Xub National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Qiying Sunb National Clinical Research Center for Geriatric Disorders , Changsha , Hunan , China.
Xiangya Hospital Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdolescentAdultAsian PeopleBrainChinaFemaleHumansInsomnia, Fatal FamilialMaleMiddle AgedPedigreePoint MutationPrion ProteinsPsychotic DisordersRetrospective StudiesYoung AdultPrion Proteinsclinical featuresFatal family insomniagene mutationgenetic characteristicspedigreePRNPthalamus

Identifiers

PMID31122137
PMCPMC6629183
OpenAlexW2946441030

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.