Evidence map›Paper›PMID 27458975›Full record

ArticleAnnals of neurology2016

Reasons Charcot-Marie-Tooth disease due to mutations in the MME gene should not be named AR-CMT2T.

Stéphane Mathis, Cyril Goizet, Meriem Tazir, Laurent Magy, Jean-Michel Vallat

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Annals of neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Stéphane MathisDepartment of Neurology, Poitiers University Hospital Center, Poitiers, France.
Cyril GoizetDepartment of Medical Genetics, (national reference center "Neuromuscular Diseases of the Great Southwest"), University Hospital (Pellegrin University Hospital Center), and Maladies Rares: Génétique et Métabolisme (MRGM) Laboratory, National Institute of Health and Medical Research U1211, University of Bordeaux, Bordeaux, France.
Meriem TazirDepartment of Neurology, Mustapha Bacha University Hospital, Algiers, Algeria.
Laurent MagyDepartment of Neurology, (National reference center "Rare Peripheral Neuropathies"), Dupuytren University Hospital, Limoges, France.
Jean-Michel VallatDepartment of Neurology, (National reference center "Rare Peripheral Neuropathies"), Dupuytren University Hospital, Limoges, France.
Hôpital Dupuytren · FRHôpital Mustapha Pacha · DZUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Charcot-Marie-Tooth DiseaseMutationEndrinHumansPhenotypeEndrinMME

Identifiers

PMID27458975
OpenAlexW2488023021

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.