欠神発作、欠神てんかん
- 関
- absence epilepsy、absence seizure、absence status
WordNet
- failure to be present
- the occurrence of an abrupt, transient loss or impairment of consciousness (which is not subsequently remembered), sometimes with light twitching, fluttering eyelids, etc.; common in petit mal epilepsy (同)absence_seizure
- the state of being absent; "he was surprised by the absence of any explanation"
- the time interval during which something or somebody is away; "he visited during my absence"
- of or relating to or characteristic of epilepsy; "epileptic seizure"
- a person who has epilepsy
PrepTutorEJDIC
- 〈U〉〈C〉『るす』,不在;『欠席』;不在期間;(…を)欠席すること《+『from』+『名』》 / 〈U〉(…が)『ないこと』,(…の)欠如(lacking)《+『of』+『名』》
- てんかん[性]の / てんかん患者
UpToDate Contents
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English Journal
- Potentiation of mGlu5 receptors with the novel enhancer, VU0360172, reduces spontaneous absence seizures in WAG/Rij rats.
- D'Amore V, Santolini I, van Rijn CM, Biagioni F, Molinaro G, Prete A, Conn PJ, Lindsley CW, Zhou Y, Vinson PN, Rodriguez AL, Jones CK, Stauffer SR, Nicoletti F, van Luijtelaar G, Ngomba RT.SourceI.R.C.C.S., NEUROMED, Neuropharmacology Unit, Parco Tecnologico, Località Camerelle 86077, Pozzilli, Isernia, Italy.
- Neuropharmacology.Neuropharmacology.2013 Mar;66:330-8. doi: 10.1016/j.neuropharm.2012.05.044. Epub 2012 Jun 15.
- Absence epilepsy is generated by the cortico-thalamo-cortical network, which undergoes a finely tuned regulation by metabotropic glutamate (mGlu) receptors. We have shown previously that potentiation of mGlu1 receptors reduces spontaneous occurring spike and wave discharges (SWDs) in the WAG/Rij rat
- PMID 22705340
- Differential seizure response in two models of cortical heterotopia.
- Gabel LA, Manglani M, Ibanez N, Roberts J, Ramos RL, Rosen GD.SourceDepartment of Psychology, Lafayette College, Easton, PA, United States; Program in Neuroscience, Lafayette College, Easton, PA, United States. Electronic address: gabell@lafayette.edu.
- Brain research.Brain Res.2013 Feb 4;1494:84-90. doi: 10.1016/j.brainres.2012.11.040. Epub 2012 Nov 29.
- Malformations of cortical development (MCD) are linked to epilepsy in humans. MCD encompass a broad spectrum of malformations, which occur as the principal pathology or a secondary disruption. Recently, Rosen et al. (2012) reported that BXD29-Trl4(lps-2J)/J mice have subcortical nodular heterotopias
- PMID 23201443
- Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype.
- Cordelli DM, Garavelli L, Savasta S, Guerra A, Pellicciari A, Giordano L, Bonetti S, Cecconi I, Wischmeijer A, Seri M, Rosato S, Gelmini C, Della Giustina E, Ferrari AR, Zanotta N, Epifanio R, Grioni D, Malbora B, Mammi I, Mari F, Buoni S, Mostardini R, Grosso S, Pantaleoni C, Doz M, Poch-Olivé ML, Rivieri F, Sorge G, Simonte G, Licata F, Tarani L, Terazzi E, Mazzanti L, Cerruti Mainardi P, Boni A, Faravelli F, Grasso M, Bianchi P, Zollino M, Franzoni E.SourceChild Neurology and Psychiatry Unit, S Orsola Malpighi Hospital, University of Bologna, Italy. ducciomaria.cordelli@aosp.bo.it.
- American journal of medical genetics. Part A.Am J Med Genet A.2013 Feb;161(2):273-84. doi: 10.1002/ajmg.a.35717. Epub 2013 Jan 15.
- Mowat-Wilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of the ZEB2 gene and is characterized by distinctive facial features, epilepsy, moderate to severe intellectual disability, corpus callosum abnormalities and other congenital malformations. Epilepsy is con
- PMID 23322667
Japanese Journal
- 日本脳炎ワクチン接種後てんかん発作が急性増悪した一例
- Advances on genetic rat models of epilepsy
- 非けいれん性てんかん重積状態を初発症状とした前頭葉てんかんの1小児例
Related Links
- Hello! My 9 year old daughter was diagnosed with absence epilepsy on 3 April 2014. She is currently taking Epilum CR 300 twice a day, as well as 5mg Sibelium once a day to prevent migraines. She is on quite an emotional ...
- Learn more from WebMD about absence seizures, a symptom of epilepsy. ... Typically, this type of seizure lasts between 10 and 30 seconds. The person, most often a child aged 5 to 15, abruptly stops whatever he's doing (talking ...
Related Pictures
★リンクテーブル★
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- 関
- absence seizure、complex partial status epilepticus、epileptic absence、generalized convulsive status epilepticus、generalized status epilepticus、non-convulsive status epilepticus、status epilepticus
[★]
- 英
- absence epilepsy、epileptic absence
- 関
- 欠神発作、小発作性てんかん、小児欠神てんかん、若年性欠神てんかん
[★]
欠神てんかん
- 関
- absence seizure、childhood absence epilepsy、epileptic absence、juvenile absence epilepsy、petit mal epilepsy
[★]
- 関
- absent、defect、deficiency、lack、morphological defect、nonexistent
[★]
- (医)てんかんの/てんかん性の。癲癇にかかったような、痙攣的な
- 関
- epilepsia, epilepsy, seizure