Evidence map›Paper›PMID 35587630›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2022

De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic Dyskinesia.

Thomas Wirth, Aurélie Méneret, Nathalie Drouot, Gabrielle Rudolf, Ouhaid Lagha Boukbiza, Jamel Chelly, Christine Tranchant, Amélie Piton, Emmanuel Roze, Mathieu Anheim

Abstract readLetterComment
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2022. 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. Review
  3. Article
  4. Article
  5. Two Cases ofMovement disorders clinical practice · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Thomas Wirth *Service de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.ORCID 0000-0002-4427-5765
Aurélie Méneret *Département de neurologie, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, Paris, France.ORCID 0000-0002-7623-1142
Nathalie DrouotInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Institut National de la Santé Et de la Recherche Médicale-U964/Centre National de la Recherche Scientifique-UMR7104/Université de Strasbourg, Illkirch-Graffenstaden, France.
Gabrielle RudolfService de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Ouhaid Lagha BoukbizaService de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Jamel ChellyInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Institut National de la Santé Et de la Recherche Médicale-U964/Centre National de la Recherche Scientifique-UMR7104/Université de Strasbourg, Illkirch-Graffenstaden, France.
Christine TranchantService de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Amélie PitonInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Institut National de la Santé Et de la Recherche Médicale-U964/Centre National de la Recherche Scientifique-UMR7104/Université de Strasbourg, Illkirch-Graffenstaden, France.
Emmanuel Roze *Département de neurologie, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, Paris, France.
Mathieu Anheim *Service de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ChoreaDystoniaHumansMutation

Identifiers

PMID35587630
PMCPMC9321051

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.