Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
about
Analyzing clinical and electrophysiological characteristics of Paroxysmal DyskinesiaA new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic studyDiagnosis and treatment of dystoniaPRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.Paroxysmal Dyskinesia in Border Terriers: Clinical, Epidemiological, and Genetic Investigations.Paroxysmal dyskinesias in miceParoxysmal dyskinesias.Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.The startle syndromes: physiology and treatment.Chorea and related disorders.Use of antiepileptic drugs for hyperkinetic movement disorders.PRRT2-related disorders: further PKD and ICCA cases and review of the literature.Diagnostic issues in childhood and adult dystonia.Episodic movement disorders: from phenotype to genotype and back.The evolving spectrum of PRRT2-associated paroxysmal diseases.Adult onset startle epilepsy.Pathological laughter associated with paroxysmal kinesigenic dyskinesia: A rare presentation of acute disseminated encephalomyelitis.Clinical manifestations in paroxysmal kinesigenic dyskinesia patients with proline-rich transmembrane protein 2 gene mutation.Diagnosis and treatment of paroxysmal kinesigenic dyskinesia in a 15-year-old boy.Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation.Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.Secondary paroxysmal dyskinesias.Paroxysmal kinesigenic choreoathetosis because of cryptogenic myelitis. Remission with carbamazepine and the pathogenetic role of altered sodium channels.A case of paroxysmal kinesigenic dyskinesia with spastic paraparesis.Acetazolamide-responsive paroxysmal dyskinesia in a 12-week-old female golden retriever dog.Abnormal Somatosensory Synchronization in Patients With Paroxysmal Kinesigenic Dyskinesia: A Magnetoencephalographic Study.Familial Paroxysmal Kinesigenic Dyskinesia is associated with mutations in the KCNA1 gene.PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesia.Altered inhibitory modulation of somatosensory cortices in paroxysmal kinesigenic dyskinesia.Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene
P2860
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P2860
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
description
1999 nî lūn-bûn
@nan
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@ast
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@en
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@nl
type
label
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@ast
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@en
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@nl
prefLabel
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@ast
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@en
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@nl
P2093
P356
P1433
P1476
Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
@en
P2093
P2888
P304
P356
10.1007/S004150050318
P577
1999-02-01T00:00:00Z
P6179
1050823495