Evidence map›Paper›PMID 32812416›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2020

A Novel Coincidence: Essential Thrombocythemia with Facioscapulohumeral Muscular Dystrophy

Ceren Hangül, Orhan Kemal Yücel, Aslı Toylu, Hilmi Uysal, Sibel Berker Karaüzüm

Abstract readCase Reports
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2020. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Review
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

5 authors.

Ceren HangülAkdeniz University Faculty of Medicine, Department of Medical Biology and Genetics, Antalya, Turkey
Orhan Kemal YücelAkdeniz University Faculty of Medicine, Department of Hematology, Antalya, Turkey
Aslı ToyluAkdeniz University Faculty of Medicine, Department of Medical Genetics, Antalya, TurkeyORCID 0000-0002-5531-6825
Hilmi UysalAkdeniz University Faculty of Medicine, Department of Neurology, Antalya, TurkeyORCID 0000-0002-6063-377X
Sibel Berker KaraüzümAkdeniz University Faculty of Medicine, Department of Medical Biology and Genetics, Antalya, TurkeyORCID 0000-0002-6338-7623

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdolescentBiomarkersDisease SusceptibilityGenetic TestingHumansMaleMuscular Dystrophy, FacioscapulohumeralMutationPhenotypeThrombocythemia, EssentialBiomarkersEssential thrombocythemiaETFacioscapulohumeral Muscular DystrophyFSHDJAK2 p.V617F mutation

Identifiers

PMID32812416
PMCPMC7702655

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.