Evidence map›Paper›PMID 27844164›Full record

ArticleJournal of neurology2017

Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt-Jakob disease due to V203I heterozygous mutation in the PRNP gene.

A Cistaro, L Cassalia, C Ferrara, C Atzori, D Vai, N Quartuccio, P Fania, G P Vaudano, D Imperiale

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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. Article
  2. A longitudinalJournal of neurology · 2022
    Article
  3. Article
  4. 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

9 authors.

A CistaroPositron Emission Tomography Centre IRMET, S.p.A., Affidea, V. O. Vigliani 89, 10136, Turin, Italy. angelina.cistaro@affidea.it.ORCID http://orcid.org/0000-0001-8024-8425
L CassaliaNuclear Medicine Unit, Department of Biomedical Sciences and of Mophologic and Functional Images, University of Messina, Messina, Italy.
C FerraraNuclear Medicine Unit Department, P.O. Umberto I, Siracusa, Italy.
C AtzoriNeurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.
D VaiNeurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.
N QuartuccioWolfson Molecular Imaging Centre, The University of Manchester, Manchester, UK.
P FaniaPositron Emission Tomography Centre IRMET, S.p.A., Affidea, V. O. Vigliani 89, 10136, Turin, Italy.
G P VaudanoNeuroradiology Unit, ASL TO2 San Giovanni Bosco Hospital, Turin, Italy.
D ImperialeNeurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationPositron Emission Tomography Computed TomographyBrainCreutzfeldt-Jakob SyndromeFemaleFluorodeoxyglucose F18HeterozygoteHumansMiddle AgedPrion ProteinsRadiopharmaceuticalsFluorodeoxyglucose F18Prion ProteinsPRNP protein, humanRadiopharmaceuticals

Identifiers

PMID27844164

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.