Evidence map›Paper›PMID 30793011›Full record

ArticleChild neurology open2019

A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?

Roberta Milone, Riccardo Masson, Caterina Di Cosmo, Massimo Tonacchera, Veronica Bertini, Andrea Guzzetta, Roberta Battini

Abstract read
In one paragraph

Article in Child neurology open, 2019. 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. Review
  2. Article
  3. Chorea in children: etiology, diagnostic approach and management.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  4. Article
  5. 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

7 authors.

Roberta MiloneDepartment of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.ORCID https://orcid.org/0000-0001-7557-6598
Riccardo MassonDevelopmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Caterina Di CosmoDepartment of Endocrinology, AOUP, Pisa, Italy.
Massimo TonaccheraDepartment of Endocrinology, AOUP, Pisa, Italy.
Veronica BertiniSection of Cytogenetics, Medicine of Laboratory Department, AOUP, Pisa, Italy.
Andrea GuzzettaDepartment of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.
Roberta BattiniDepartment of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.ORCID https://orcid.org/0000-0002-7889-1355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ataxiaautism spectrum disorderhypotoniaintellectual disabilitymotor delay

Identifiers

PMID30793011
PMCPMC6376510

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.