Evidence map›Paper›PMID 19761452›Full record

ArticleEpilepsia2009

Animal models of focal cortical dysplasia and tuberous sclerosis complex: recent progress toward clinical applications.

Michael Wong

Abstract read
In one paragraph

Article in Epilepsia, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Neuroinflammation: A Signature or a Cause of Epilepsy?International journal of molecular sciences · 2021
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Activation of extracellular regulated kinase and mechanistic target of rapamycin pathway in focal cortical dysplasia.Neuropathology : official journal of the Japanese Society of Neuropathology · 2016
    Article
  17. Article
  18. Past and present definitions of epileptogenesis and its biomarkers.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2014
    Review
  19. Review
  20. 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

1 author.

Michael WongDepartment of Neurology and the Hope Center for Neurological Disorders, Washington University School of Medicine, St Louis, Missouri 63110, USA. wong_m@wustl.edu

Funding

MECHANISMS OF BRAIN DYSFUNCTION IN TUBEROUS SCLEROSISR01NS056872 · NINDS · WASHINGTON UNIVERSITY · PI WONG, MICHAEL · 2006 to 2019
$4.0M
Rapid seizure-induced changes in dendritic spinesK02NS045583 · NINDS · WASHINGTON UNIVERSITY · PI WONG, MICHAEL · 2003 to 2007
$714k
NINDS NIH HHS K02 NS045583NINDS NIH HHS R01 NS056872
6 · The paper itself

Abstract

Focal cortical dysplasia (FCD) and related malformations of cortical development (MCDs) represent an increasingly recognized cause of medically intractable epilepsy. However, the underlying mechanisms of epileptogenesis are poorly understood, and treatments for epilepsy due to various cortical malformations are often limited or ineffective. Animal models offer a number of advantages for investigating cellular and molecular mechanisms of epileptogenesis and developing novel, rational therapies for MCD-related epilepsy. This review highlights specific examples of how animal models have been useful in addressing several clinically relevant issues about epilepsy due to FCDs and related cortical malformations, including the pathologic and clinical features, etiologic factors, localization of the epileptogenic zone, neuronal and astrocytic contributions to epileptogenesis, and the development of antiepileptogenic therapies.

Indexed as

Disease Models, AnimalAnimalsAnticonvulsantsCerebral CortexDrug DesignEpilepsyHumansMalformations of Cortical DevelopmentMechanistic Target of Rapamycin Complex 1MiceMice, KnockoutMultiprotein ComplexesProteinsRatsSirolimusTOR Serine-Threonine KinasesAnticonvulsantsMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesProteinsSirolimusTOR Serine-Threonine KinasesTranscription Factors

Identifiers

PMID19761452
PMCPMC3934654

What OpenQuestion holds

Textmetadata
LicenceTDM
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.