Evidence map›Paper›PMID 36873433›Full record

ArticleFrontiers in neurology2023

The most common European HINT1 neuropathy variant phenotype and its case studies.

Marija Rozevska, Dmitrijs Rots, Linda Gailite, Ronalds Linde, Stanislavs Mironovs, Maksims Timcenko, Viktors Linovs, Dzintra Locmele, Ieva Micule, Baiba Lace and 1 more

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

Article in Frontiers in neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

11 authors at 3 institutions in 1 country.

Marija RozevskaMedical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga, Latvia.
Dmitrijs RotsMedical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga, Latvia.
Linda GailiteScientific Laboratory of Molecular Genetics, Riga Stradins University, Riga, Latvia.
Ronalds LindeRare Neurological Disease Department, Pauls' Stradins University Hospital, Riga, Latvia.
Stanislavs MironovsRare Neurological Disease Department, Pauls' Stradins University Hospital, Riga, Latvia.
Maksims TimcenkoRadiology Department, Riga 2nd Hospital, Riga, Latvia.
Viktors LinovsRadiology Department, Riga 2nd Hospital, Riga, Latvia.
Dzintra LocmeleMedical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga, Latvia.
Ieva MiculeMedical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga, Latvia.
Baiba LaceMedical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga, Latvia.
Viktorija KeninaMedical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga, Latvia.
Children's Clinical University Hospital · LVPauls Stradiņš Clinical University Hospital · LVRiga Stradiņš University · LV

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HINT1 is an ubiquitous homodimeric purine phosphoramidase belonging to the histidine-triad superfamily. In neurons, HINT1 stabilizes the interaction of different receptors and regulates the effects of their signaling disturbances. Changes in

Indexed as

axonal polyneuropathyHINT1impaired mental performancenerve USGpopulation frequency

Identifiers

PMID36873433
PMCPMC9981799
OpenAlexW4321240419

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.