Evidence map›Paper›PMID 36533587›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2022

Reply to: "GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia Phenotype".

Thomas Wirth, Giacomo Garone, Manju A Kurian, Amélie Piton, Emmanuel Roze, Jean Pierre Lin, Christine Tranchant, Laura Cif, Diane Doummar, Mathieu Anheim

Abstract readLetterComment
PubMed Publisher
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Novel missense variant in the TMEM151A gene causing paroxysmal kinesigenic dyskinesia: a case report with literature review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Thomas WirthDépartement de Neurologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.ORCID 0000-0002-4427-5765
Giacomo GaroneDepartment of Neuroscience, Mental Health and Sensory Organs, Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy.
Manju A KurianMolecular Neurosciences, Developmental Neurosciences, University College London Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0003-3529-5075
Amélie PitonFédération de Médecine Translationnelle de Strasbourg, Université de Strasbourg, Strasbourg, France.
Emmanuel RozeSorbonne Université/ Institut National de la Santé Et de la Recherche Médicale U1127/Centre National de la Recherche Scientifique Unité Mixte de Recherche 7225/Institut du Cerveau, Paris, France.
Jean Pierre LinChildren's Neurosciences Department, Evelina London Children's Hospital, Guy's and St Thomas National Health Service Foundation Trust; Women and Children's Institute, London, UK.ORCID 0000-0001-9314-2259
Christine TranchantDépartement de Neurologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Laura CifDépartement de Neurochirurgie, Unité des Pathologies Cérébrales Résistantes, Unité de Recherche sur les Comportements et Mouvements Anormaux, Hôpital Gui de Chauliac, Centre Hospitalier Régional Montpellier, Montpellier, France.ORCID 0000-0003-4920-4234
Diane DoummarSorbonne Université, Service de Neuropédiatrie-Pathologie du développement, centre de référence neurogénétique, Hôpital Trousseau AP-HP.SU, Paris, France.
Mathieu AnheimDépartement de Neurologie, Hôpital de Hautepierre, 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

DystoniaMovement DisordersGTP-Binding Protein alpha Subunits, Gi-GoHaploinsufficiencyHumansPhenotypeGNAO1 protein, humanGTP-Binding Protein alpha Subunits, Gi-Go

Identifiers

PMID36533587

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.