Evidence map›Paper›PMID 17561408›Full record

ArticleNeurobiology of disease2007

Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice.

Rajiv Devanagondi, Kiyoshi Egami, Mark S LeDoux, Ellen J Hess, H A Jinnah

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of disease, 2007. 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
0.3field-weighted citation impact, top 49% 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, 23 citations in OpenAlex.

  1. Discovery of the First Selective MACS pharmacology & translational science · 2021
    Article
  2. Dystonia and Cerebellum: From Bench to Bedside.Life (Basel, Switzerland) · 2021
    Review
  3. Article
  4. A new knock-in mouse model of l-DOPA-responsive dystonia.Brain : a journal of neurology · 2015
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Convergent mechanisms in etiologically-diverse dystonias.Expert opinion on therapeutic targets · 2011
    Review
  10. Review
  11. Article
  12. Paroxysmal dyskinesias in mice.Movement disorders : official journal of the Movement Disorder Society · 2008
    Article
  13. Experimental Models of Absence Epilepsy.Basic and clinical neuroscience
    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

5 authors at 2 institutions in 1 country.

Rajiv DevanagondiDepartment of Neurology, Meyer Room 6-181, 600 North Wolfe Street, Johns Hopkins Hospital, Baltimore, MD 21287, and University of Tennessee, Memphis 38163, USA.
Kiyoshi Egami
Mark S LeDoux
Ellen J Hess
H A Jinnah
Johns Hopkins Hospital · USUniversity of Tennessee Health Science Center · US

Funding

Pathophysiology of dystonia: animal modelsR01NS033592 · NINDS · JOHNS HOPKINS UNIVERSITY · PI HESS, ELLEN J. · 2001 to 2010
$3.5M
NEUROBIOLOGY OF DYSTONIAR01NS040470 · NINDS · JOHNS HOPKINS UNIVERSITY · PI JINNAH, HYDER A · 2000 to 2008
$2.5M
Mutant Gene Identification in the Dystonic RatR01NS048458 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI LEDOUX, MARK S · 2005 to 2008
$800k
MOLECULAR BASIS OF THE TOTTERING PHENOTYPER29NS033592 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HESS, ELLEN J. · 1995 to 1999
–
NINDS NIH HHS NS048458NINDS NIH HHS NS33592NINDS NIH HHS NS40470NINDS NIH HHS R01 NS033592NINDS NIH HHS R01 NS040470NINDS NIH HHS R01 NS048458NINDS NIH HHS R29 NS033592
6 · The paper itself

Abstract

The paroxysmal dyskinesias are a group of neurological disorders described by intermittent attacks of involuntary abnormal movements superimposed on a relatively normal baseline. The neuroanatomical substrates for these attacks are not fully understood, though available evidence from studies of affected people and animal models points to dysfunction in the basal ganglia or cerebellum. In the current studies, the anatomical basis for paroxysmal dyskinesias in lethargic mice was determined via histochemical methods sensitive to changes in regional brain activity followed by surgical elimination of the suspected source. Cytochrome oxidase histochemistry revealed increased activity in the red nucleus. Surgical removal of the cerebellum worsened ataxia but eliminated paroxysmal dyskinesias. These studies support the hypothesis that abnormal cerebellar output contributes to paroxysmal dyskinesias.

Indexed as

AnimalsBehavior, AnimalCalcium ChannelsCerebellumChoreaElectron Transport Complex IVGenes, fosImmunohistochemistryIn Situ HybridizationMiceMice, Neurologic MutantsRed NucleusCacnb4 protein, mouseCalcium ChannelsElectron Transport Complex IV

Identifiers

PMID17561408
PMCPMC10759181
OpenAlexW1970482417

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.