Evidence map›Paper›PMID 39361253›Full record

ArticleEpilepsia open2024

Sleep disturbances in SCN8A-related disorders.

Francesca Furia, Katrine M Johannesen, Claudia M Bonardi, Roberto Previtali, Angel Aledo-Serrano, Massimo Mastrangelo, Jacopo Favaro, Silvia Masnada, Valentina di Micco, Jacopo Proietti and 6 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Epilepsia open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

16 authors.

Francesca FuriaDepartment of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center, Dianalund, Denmark.ORCID https://orcid.org/0000-0002-4893-9768
Katrine M JohannesenDepartment of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center, Dianalund, Denmark.ORCID https://orcid.org/0000-0002-7356-3109
Claudia M BonardiDepartment of Woman's and Child's Health, University Hospital of Padua, Padua, Italy.ORCID https://orcid.org/0000-0002-3951-9921
Roberto PrevitaliPediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.ORCID https://orcid.org/0000-0002-3295-0655
Angel Aledo-SerranoEpilepsy and Neurogenetics Unit, Vithas La Milagrosa University Hospital, Vithas Hospital Group, Madrid, Spain.ORCID https://orcid.org/0000-0003-4889-3365
Massimo MastrangeloIRCCS Policlinico San Donato, Milan, Italy.
Jacopo FavaroDepartment of Woman's and Child's Health, University Hospital of Padua, Padua, Italy.ORCID https://orcid.org/0000-0002-4340-2398
Silvia MasnadaPediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.ORCID https://orcid.org/0000-0003-3850-8849
Valentina di MiccoEpilepsy and Movement Disorders Neurology Unit, Bambino Gesú Children Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-9011-7143
Jacopo ProiettiInnovation Biomedicine Section, Department of Engineering for Innovation Medicine, University of Verona, Verona, Italy.ORCID https://orcid.org/0000-0002-5584-4724
Pierangelo VeggiottiPediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.ORCID https://orcid.org/0000-0003-2851-3441
Guido RubboliDepartment of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center, Dianalund, Denmark.ORCID https://orcid.org/0000-0002-5309-2514
Gaetano CantalupoInnovation Biomedicine Section, Department of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
Kern OlofssonDepartment of Pediatric Epilepsy, Danish Epilepsy Center, Dianalund, Denmark.
Rikke S MøllerDepartment of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center, Dianalund, Denmark.ORCID https://orcid.org/0000-0002-9664-1448
Elena GardellaDepartment of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center, Dianalund, Denmark.ORCID https://orcid.org/0000-0002-7138-6022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

NAV1.6 Voltage-Gated Sodium ChannelSleep Wake DisordersAdolescentAdultChildChild, PreschoolElectroencephalographyEpilepsyFemaleHumansMaleNeurodevelopmental DisordersPolysomnographyYoung AdultNAV1.6 Voltage-Gated Sodium ChannelSCN8A protein, humandevelopmental and epileptic encephalopathy (DEE)epilepsySCN8Asleep disorders

Identifiers

PMID39361253
PMCPMC11633700

What OpenQuestion holds

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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.