%D8%AE%D9%84%D9%84_%D8%A7%D9%84%D8%AD%D8%B1%D9%83%D8%A9Discin%C3%A8siaDyskinesiDyskinesiaDiscinesia%D8%AF%DB%8C%D8%B3%DA%A9%DB%8C%D9%86%D8%B2%DB%8CDyskin%C3%A9sie%D7%93%D7%99%D7%A1%D7%A7%D7%99%D7%A0%D7%96%D7%99%D7%94Discinesia%E3%82%B8%E3%82%B9%E3%82%AD%E3%83%8D%E3%82%B8%E3%82%A2DyskinesiaDyskinesieDyskinezyDiscinesiaDiskinezija%D0%94%D0%B8%D1%81%D0%BA%D0%B8%D0%BD%D0%B5%D0%B7%D0%B8%D1%98%D0%B0DyskinesiQ629444
about
Presynaptic Mechanisms of l-DOPA-Induced Dyskinesia: The Findings, the Debate, and the Therapeutic ImplicationsLevetiracetam Ameliorates L-DOPA-Induced Dyskinesia in Hemiparkinsonian Rats Inducing Critical Molecular Changes in the StriatumLoss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.Pyridoxal 5 phosphate for neuroleptic-induced tardive dyskinesiaAnticholinergics for neuroleptic-induced parkinsonism and tardive dyskinesiaPyridoxal 5 phosphate for neuroleptic-induced tardive dyskinesiaGamma-aminobutyric acid agonists for neuroleptic-induced tardive dyskinesiaCalcium channel blockers for neuroleptic-induced tardive dyskinesiaVitamin E for neuroleptic-induced tardive dyskinesiaCholecystectomy for suspected gallbladder dyskinesiaCholecystectomy versus no cholecystectomy for suspected gallbladder dyskinesiaNeuroleptic reduction and/or cessation and neuroleptics as specific treatments for tardive dyskinesiaNon-neuroleptic catecholaminergic drugs for neuroleptic-induced tardive dyskinesiaBenzodiazepines for neuroleptic-induced tardive dyskinesiaGamma-aminobutyric acid agonists for neuroleptic-induced tardive dyskinesiaCalcium channel blockers for neuroleptic-induced tardive dyskinesiaMiscellaneous treatments for neuroleptic-induced tardive dyskinesiaAmantadine for dyskinesia in Parkinson's diseaseBenzodiazepines for neuroleptic-induced tardive dyskinesiaHomozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneThe human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesiaAxonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryIdentification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesiaGain-of-function ADCY5 mutations in familial dyskinesia with facial myokymiaMislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesiaMutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationExome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesiaA common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesiaMutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructureWhole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesiaPrimary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutationsDopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesiaMutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia.Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesiaCCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationAxonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesiaCongenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaMutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein armsMutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia.
P921
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P921
description
Mugimenduak egiteko arazo patologiko oro
@eu
human disease
@en
расстройство координированных двигательных актов
@ru
مرض يصيب الإنسان
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name
Diskinezija
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Dyskinesi
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Dyskinesi
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Dyskinesia
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Dyskinezy
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discinesia
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discinesia
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discinesia
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discinèsia
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diszinesia
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type
label
Diskinezija
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Dyskinesi
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Dyskinesi
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Dyskinesia
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Dyskinezy
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discinesia
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discinesia
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discinesia
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discinèsia
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diszinesia
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altLabel
运动障碍
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prefLabel
Diskinezija
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Dyskinesi
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Dyskinesi
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Dyskinesia
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Dyskinezy
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discinesia
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discinesia
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discinesia
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discinèsia
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diszinesia
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P672
P486
P508
P5806
P6366
P646
P1296
P1461
Abnormal-Involuntary-Movements
P1748
P1995
P3417
Dyskinesia
P3827
dyskinesia
P4746
P486
P5806
P6366
2780405171
P646
P672
C10.228.662.262
C10.597.350
C23.888.592.350