Evidence map›Paper›PMID 30746413›Full record

ArticleMovement disorders clinical practice2019

Is Benign Hereditary Chorea Really Benign? Brain-Lung-Thyroid Syndrome Caused by

Mered Parnes, Hassaan Bashir, Joseph Jankovic

Open access · bronzeAbstract read
In one paragraph

Article in Movement disorders clinical practice, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.Movement disorders : official journal of the Movement Disorder Society · 2026
    Observational
  5. Update on Genetic Chorea.European journal of neurology · 2025
    Review
  6. Article
  7. Review
  8. Haploinsufficiency ofIntractable & rare diseases research · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Chorea in children: etiology, diagnostic approach and management.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  14. Review of Hereditary and Acquired Rare Choreas.Tremor and other hyperkinetic movements (New York, N.Y.) · 2020
    Review
  15. The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus.Movement disorders : official journal of the Movement Disorder Society · 2020
    Article
  16. 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

3 authors at 1 institution in 1 country.

Mered ParnesPediatric Movement Disorders Clinic, Blue Bird Circle Clinic for Pediatric Neurology, Section of Pediatric Neurology and Developmental Neuroscience Texas Children's Hospital Houston Texas USA.ORCID https://orcid.org/0000-0003-2102-4282
Hassaan BashirParkinson's Disease Center and Movement Disorders Clinic, Department of Neurology Baylor College of Medicine Houston Texas USA.
Joseph JankovicParkinson's Disease Center and Movement Disorders Clinic, Department of Neurology Baylor College of Medicine Houston Texas USA.
Baylor College of Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSince its localization to the

methodsThe phenomenology of movement disorders and other symptomatology associated with mutations in

resultsWe studied 5 patients (3 females), ages 2 to 31 years, with confirmed pathogenic variants in

conclusionsThe phenotype associated with pathogenic variants in

Indexed as

benign hereditary choreabrain‐lung‐thyroid disorderbrain‐lung‐thyroid syndromeNKX2‐1TTF‐1

Identifiers

PMID30746413
PMCPMC6335533
OpenAlexW2895581552

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.