Evidence map›Paper›PMID 15742102›Full record

ArticleJournal of neurology2005

Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.

Giovanni Coppola, Chiara Criscuolo, Giuseppe De Michele, Salvatore Striano, Fabrizio Barbieri, Pasquale Striano, Anna Perretti, Lucio Santoro, Vincenzo Brescia Morra, Francesco Saccà and 7 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2005. 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
0.8field-weighted citation impact, top 29% 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, 9 citations in OpenAlex.

  1. Variants inBrain communications · 2021
    Article
  2. 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

17 authors at 4 institutions in 2 countries.

Giovanni CoppolaDipartimento di Scienze Neurologiche, Università degli Studi di Napoli Federico II, Via Pansini 5, 80131, Napoli, Italy.
Chiara Criscuolo
Giuseppe De Michele
Salvatore Striano
Fabrizio Barbieri
Pasquale Striano
Anna Perretti
Lucio Santoro
Vincenzo Brescia Morra
Francesco Saccà
Valentina Scarano
Adamo P D'Adamo
Sandro Banfi
Paolo Gasparini
Filippo M Santorelli
Anna E Lehesjoki
Alessandro Filla
University of Naples Federico II · ITTelethon Institute Of Genetics And Medicine · ITSapienza University of Rome · ITUniversity of Helsinki · FI

Funding

Telethon TGM03Z03Telethon TGM06S01
6 · The paper itself

Abstract

We describe two couples of sibs from a southern Italian family affected by epilepsy, myoclonus, mental retardation and slight ataxia. Onset was between 4 and 12 years and the course slowly progressive. The clinical picture suggested the diagnosis of Unverricht-Lundborg disease. Molecular study excluded linkage to EPM1. Other possible causes of progressive myoclonus epilepsy were also excluded.

Indexed as

AdultAge of OnsetAtaxiaDNA, MitochondrialDNA Mutational AnalysisFamily HealthFemaleHumansIntellectual DisabilityMagnetic Resonance ImagingMyoclonic Epilepsies, ProgressivePoint MutationDNA, Mitochondrial

Identifiers

PMID15742102
OpenAlexW1984809570

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.