Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.
about
Dystonia and Paroxysmal Dyskinesias: Under-Recognized Movement Disorders in Domestic Animals? A Comparison with Human Dystonia/Paroxysmal Dyskinesias.The clinical and genetic heterogeneity of paroxysmal dyskinesias.Functional dystonia and the borderland between neurology and psychiatry: New concepts.International veterinary epilepsy task force consensus proposal: diagnostic approach to epilepsy in dogsADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesiasA homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia.Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients.Aberrant transcriptional networks in step-wise neurogenesis of paroxysmal kinesigenic dyskinesia-induced pluripotent stem cells.Phenotype-specific diagnosis of functional (psychogenic) movement disorders.Intermittent head drops: the differential spectrum.The evolving spectrum of PRRT2-associated paroxysmal diseases.Novel Dystonia Genes: Clues on Disease Mechanisms and the Complexities of High-Throughput Sequencing.Expanding the genetic spectrum of paroxysmal dyskinesias.Atypical Manifestations in Glut1 Deficiency Syndrome.The epileptic and nonepileptic spectrum of paroxysmal dyskinesias: Channelopathies, synaptopathies, and transportopathies.Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome.A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification.[Parasomnia and paroxysmal dyskinesia].Paroxysmal kinesigenic dyskinesia caused by 16p11.2 microdeletion.Rethinking status dystonicus.Thalamocortical dysconnectivity in paroxysmal kinesigenic dyskinesia: Combining functional magnetic resonance imaging and diffusion tensor imaging.Treatment of paroxysmal dyskinesias in children.ECHS1 deficiency-associated paroxysmal exercise-induced dyskinesias: case presentation and initial benefit of intervention.Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency.Myotonia Congenita Can Be Mistaken as Paroxysmal Kinesigenic Dyskinesia.De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.Dystonia.Long-Term Effect of GPi-DBS in a Patient With Generalized Dystonia Due to GLUT1 Deficiency Syndrome.
P2860
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P2860
Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
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name
Paroxysmal dyskinesias revisit ...... ases and a new classification.
@en
type
label
Paroxysmal dyskinesias revisit ...... ases and a new classification.
@en
prefLabel
Paroxysmal dyskinesias revisit ...... ases and a new classification.
@en
P2860
P356
P1433
P1476
Paroxysmal dyskinesias revisit ...... ases and a new classification.
@en
P2093
Una-Marie Sheerin
P2860
P304
P356
10.1002/MDS.25933
P407
P577
2014-06-25T00:00:00Z