Evidence map›Paper›PMID 33015227›Full record

ArticleMovement disorders clinical practice2020

Aceruloplasminemia Presenting with Asymmetric Chorea Due to a Novel Frameshift Mutation.

Sabiha T Aydemir, Onur Bulut, Serdar Ceylaner, Muhittin C Akbostancı

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Movement disorders clinical practice, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. One Side of the Story; Clues to Etiology in Patients with Asymmetric Chorea.Tremor and other hyperkinetic movements (New York, N.Y.) · 2022
    Review
  4. 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

4 authors at 2 institutions in 1 country.

Sabiha T AydemirDepartment of Neurology Ankara University School of Medicine Ankara Turkey.
Onur BulutDepartment of Neurology Ankara University School of Medicine Ankara Turkey.
Serdar CeylanerIntergen Genetics and Rare Diseases Diagnosis Research & Application Center, Ibni Sina Hastanesi, Noroloji Bolumu, K Blok, 3. Kat, 06100 Altindag Ankara Turkey.
Muhittin C AkbostancıDepartment of Neurology Ankara University School of Medicine Ankara Turkey.
Ankara University · TRIntergen (Turkey) · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

aceruloplasminemia, asymmetrical signs

Identifiers

PMID33015227
PMCPMC7525192
OpenAlexW3091093634

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.