Evidence map›Paper›PMID 31871823›Full record

ArticleTremor and other hyperkinetic movements (New York, N.Y.)2019

Generalized Dystonia and Paroxysmal Dystonic Attacks due to a Novel

Carlos Zúñiga-Ramírez, Mirelle Kramis-Hollands, Rodrigo Mercado-Pimentel, Héctor Alberto González-Usigli, Michel Sáenz-Farret, Alberto Soto-Escageda, Alfonso Fasano

Open access · greenAbstract readCase Reports
In one paragraph

Article in Tremor and other hyperkinetic movements (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Clinical and Genetic Spectrum ofNeurology. Genetics · 2026
    Article
  2. Deep Brain Stimulation in Leigh-Like Syndrome Due to DNM1 Pathogenic Variant.Tremor and other hyperkinetic movements (New York, N.Y.) · 2025
    Article
  3. Article
  4. Review
  5. Genetic Testing of Movements Disorders: A Review of Clinical Utility.Tremor and other hyperkinetic movements (New York, N.Y.) · 2024
    Review
  6. Tremor and other hyperkinetic movements (New York, N.Y.) · 2024
    Article
  7. Article
  8. Genetic updates on paroxysmal dyskinesias.Journal of neural transmission (Vienna, Austria : 1996) · 2021
    Review
  9. Genetic Dystonias: Update on Classification and New Genetic Discoveries.Current neurology and neuroscience reports · 2021
    Review
  10. Article
  11. Review
  12. Treatment of Dystonia: Medications, Neurotoxins, Neuromodulation, and Rehabilitation.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Review
  13. 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 at 3 institutions in 2 countries.

Carlos Zúñiga-RamírezMovement Disorders and Neurodegenerative Diseases Unit (UMANO), Guadalajara, MX.
Mirelle Kramis-HollandsDepartment of Genetics, Hospital Español, Mexico City, MX.
Rodrigo Mercado-PimentelMovement Disorders and Neurodegenerative Diseases Unit (UMANO), Guadalajara, MX.
Héctor Alberto González-UsigliMovement Disorders and Neurodegenerative Diseases Unit (UMANO), Guadalajara, MX.
Michel Sáenz-FarretMovement Disorders and Neurodegenerative Diseases Unit (UMANO), Guadalajara, MX.
Alberto Soto-EscagedaMovement Disorders and Neurodegenerative Diseases Unit (UMANO), Guadalajara, MX.
Alfonso FasanoEdmond J. Safra Program in Parkinson's Disease and Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital and Division of Neurology, UHN, Division of Neurology, University of Toronto, Toronto, CA.
Hospital Civil de Guadalajara · MXMexican Social Security Institute · MXToronto Western Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Paroxysmal movement disorders are a heterogeneous group of neurological diseases, better understood in recent years thanks to widely available genetic testing. Case report: A pair of monozygotic twins with dystonia and paroxysmal attacks, resembling paroxysmal non-kinesigenic dyskinesias, due to a novel Discussion: Paroxysmal worsening of movement disorders should be suspected as part of the

Indexed as

Dystonic DisordersElectroencephalographyGenetic VariationHumansMaleSodium-Potassium-Exchanging ATPaseTwins, MonozygoticYoung AdultATP1A3 protein, humanSodium-Potassium-Exchanging ATPaseAHC-2ATP1A3dystoniaparoxysmal dyskinesiarapid-onset parkinsonism-dystoniastatus dystonicus

Identifiers

PMID31871823
PMCPMC6925393
OpenAlexW2998901135

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.