目次
WordNet
- of or pertaining to or characteristic of the Baltic States or their peoples or languages
- a branch of the Indo-European family of languages related to the Slavonic languages; Baltic languages have preserved many archaic features that are believed to have existed in Proto-Indo European (同)Baltic language
- a sea in northern Europe; stronghold of the Russian navy (同)Baltic_Sea
- of or near or on the Baltic Sea; "The Baltic republics"
- a clonic spasm of a muscle or muscle group
PrepTutorEJDIC
- バルト海の / バルト諸国の / 《the Bal・tic》バルト海 / 〈U〉バルト語族
UpToDate Contents
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- 1. 遺伝性運動失調の概要 overview of the hereditary ataxias
- 2. ミオクローヌスの治療 treatment of myoclonus
- 3. 小児における運動過多な運動障害 hyperkinetic movement disorders in children
- 4. 症候性（二次性）ミオクローヌス symptomatic secondary myoclonus
- 5. ミオクローヌスの分類および評価 classification and evaluation of myoclonus
English Journal
- Limited Proteolysis Reveals That Amyloids from the 3D Domain-Swapping Cystatin B Have a Non-Native β-Sheet Topology.
- Davis PJ1, Holmes D2, Waltho JP3, Staniforth RA4.
- Journal of molecular biology.J Mol Biol.2015 Jul 31;427(15):2418-34. doi: 10.1016/j.jmb.2015.05.014. Epub 2015 May 22.
- 3D domain-swapping proteins form multimers by unfolding and then sharing of secondary structure elements, often with native-like interactions. Runaway domain swapping is proposed as a mechanism for folded proteins to form amyloid fibres, with examples including serpins and cystatins. Cystatin C amyl
- PMID 26004542
- Refining the phenotype of Unverricht-Lundborg disease (EPM1): a population-wide Finnish study.
- Hyppönen J1, Äikiä M2, Joensuu T2, Julkunen P2, Danner N2, Koskenkorva P2, Vanninen R2, Lehesjoki AE2, Mervaala E2, Kälviäinen R2.
- Neurology.Neurology.2015 Apr 14;84(15):1529-36. doi: 10.1212/WNL.0000000000001466. Epub 2015 Mar 13.
- OBJECTIVE: This Finnish nationwide study aimed to refine the clinical phenotype variability and to identify factors that could explain the extensive variability in the clinical severity of the symptoms observed among patients with Unverricht-Lundborg disease (progressive myoclonus epilepsy type 1 [E
- PMID 25770194
- Reduced cortical activation in inferior frontal junction in Unverricht-Lundborg disease (EPM1) - A motor fMRI study.
- Könönen M1, Danner N2, Koskenkorva P3, Kälviäinen R4, Hyppönen J5, Mervaala E2, Karjalainen P6, Vanninen R7, Niskanen E6.
- Epilepsy research.Epilepsy Res.2015 Mar;111:78-84. doi: 10.1016/j.eplepsyres.2015.01.006. Epub 2015 Jan 24.
- BACKGROUND: Unverricht-Lundborg disease (EPM1) is characterized by stimulus-sensitive and action-activated myoclonus, tonic-clonic seizures and ataxia. Several disease-related alterations in cortical structure and excitability have been associated with the motor symptoms of EPM1. This study aimed to
- PMID 25769376
Japanese Journal
- Baltic myoclonus and Crohn's disease[Letter]
- TATE ED.
- Mov Disord 8, 252-253, 1993
- NAID 30012623954
- Identical genetic locus for Baltic and mediterranean myoclonus
- MALAFOSSE A
- Lancet 339, 1080-1081, 1992
- NAID 30005739904
Related Links
- This disease manifests between six and sixteen years and is most prevalent in Scandinavia and the Baltic countries. Myoclonus gradually becomes worse and less susceptible to medication. Cognitive decline is slow and sometimes mild.
- Baltic myoclonic epilepsy; Baltic myoclonus; Baltic myoclonus epilepsy; EPM1; Lundborg-Unverricht syndrome; Mediterranean myoclonic epilepsy; myoclonic epilepsy of Unverricht and Lundborg; PME; progressive myoclonic epilepsy ...
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