Evidence map›Paper›PMID 28660440›Full record

ArticleCerebellum (London, England)2017

Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation.

Laszlo Szpisjak, Viola L Nemeth, Noemi Szepfalusi, Denes Zadori, Zoltan Maroti, Tibor Kalmar, Laszlo Vecsei, Peter Klivenyi

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. RareInternational journal of molecular sciences · 2026
    Article
  3. Review
  4. Expanding the clinical and genetic heterogeneity of SPAX5.Annals of clinical and translational neurology · 2020
    Article
  5. 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

8 authors.

Laszlo SzpisjakDepartment of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary.
Viola L NemethDepartment of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary.
Noemi SzepfalusiDepartment of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary.
Denes ZadoriDepartment of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary.
Zoltan MarotiGenetic Diagnostic Laboratory, Department of Pediatrics and Pediatric Health Center, University of Szeged, Szeged, Hungary.
Tibor KalmarGenetic Diagnostic Laboratory, Department of Pediatrics and Pediatric Health Center, University of Szeged, Szeged, Hungary.
Laszlo VecseiDepartment of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary.
Peter KlivenyiDepartment of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary. klivenyi.peter@med.u-szeged.hu.ORCID 0000-0002-5389-3266

Funding

Hungarian Brain Research program KTIA Grant No. 13 NAP-A-II/17Hungarian Brain Research Program KTIA Grant No. 13 NAP-A-II/17
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CognitionMutation, MissenseAdultATPases Associated with Diverse Cellular ActivitiesATP-Dependent ProteasesBrainFamilyFemaleHumansMaleMiddle AgedPhenotypePilot ProjectsSpinocerebellar AtaxiasAFG3L2 protein, humanATPases Associated with Diverse Cellular ActivitiesATP-Dependent Proteases

Identifiers

PMID28660440

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.