Paroxysmal dyskinesias (Q34188473)

31 July 2017

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title

Paroxysmal dyskinesias. (English)

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Kailash Phatechand Bhatia

31 July 2017

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series ordinal

1

object named as

Kailash P Bhatia

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PubMed ID

21626559

31 July 2017

language of work or name

English

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publication date

1 May 2011

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31 July 2017

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31 July 2017

26

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31 July 2017

6

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31 July 2017

1157-1165

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Familial (idiopathic) paroxysmal dyskinesias: an update

31 July 2017

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Paroxysmal dyskinesias: clinical features and classification

21 January 2018

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Secondary paroxysmal dyskinesias

21 January 2018

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Paroxysmal dystonic choreoathetosis: A family study and review of the literature

21 January 2018

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Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes

21 January 2018

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Paroxysmal kinesigenic choreoathetosis: a report of 26 patients

21 January 2018

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Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria

21 January 2018

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Seizure induced by movement

21 January 2018

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Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis.

21 January 2018

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The relationship between paroxysmal kinesigenic choreoathetosis and epilepsy.

21 January 2018

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Corticospinal disinhibition in paroxysmal kinesigenic dyskinesia.

21 January 2018

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Abnormal cortical and spinal inhibition in paroxysmal kinesigenic dyskinesia

21 January 2018

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Ictal (99m)Tc ECD SPECT in paroxysmal kinesigenic choreoathetosis

21 January 2018

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Perfusion abnormality of the caudate nucleus in patients with paroxysmal kinesigenic choreoathetosis

21 January 2018

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Multicenter study of paroxysmal dyskinesias in Japan--clinical and pedigree analysis.

21 January 2018

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Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies

21 January 2018

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A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

21 January 2018

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Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

21 January 2018

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Sporadic and familial varieties of tonic seizures

21 January 2018

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Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.

21 January 2018

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A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.

21 January 2018

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Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

21 January 2018

1 reference

Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.

21 January 2018

1 reference

Ictal SPECT in paroxysmal non-kinesigenic dyskinesia. Case report and review of the literature

21 January 2018

1 reference

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia

21 January 2018

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Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.

21 January 2018

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The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

21 January 2018

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Familial paroxysmal dystonia induced by exercise

21 January 2018

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Paroxysmal exercise-induced dystonia: eight new sporadic cases and a review of the literature

21 January 2018

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Paroxysmal hemidystonia induced by prolonged exercise and cold

21 January 2018

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The paroxysmal dyskinesias

21 January 2018

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A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study

21 January 2018

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Exercise induced steroid dependent dystonia, ataxia, and alternating hemiplegia associated with epilepsy

21 January 2018

1 reference

Paroxysmal exercise-induced dystonia as a presenting feature of young-onset Parkinson's disease

21 January 2018

1 reference

Familial paroxysmal exercise-induced dyskinesia and benign epilepsy: a clinical and neurophysiological study of an uncommon disorder.

21 January 2018

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Analysis of stimuli triggering attacks of paroxysmal dystonia induced by exertion

21 January 2018

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Alterations of motor cortical inhibition in patients with dystonia.

21 January 2018

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Changes in perfusion pattern using ECD-SPECT indicate frontal lobe and cerebellar involvement in exercise-induced paroxysmal dystonia.

21 January 2018

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Paroxysmal movement disorders in GLUT1 deficiency syndrome

21 January 2018

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GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias

21 January 2018

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Paroxysmal dystonia induced by exercise and acetazolamide

21 January 2018

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Posteroventral pallidotomy can ameliorate attacks of paroxysmal dystonia induced by exercise

21 January 2018

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Orthostatic paroxysmal dystonia.

21 January 2018

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Episodic ataxia type 1 with distal weakness: a novel manifestation of a potassium channelopathy.

21 January 2018

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Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo).

21 January 2018

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Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine

21 January 2018

1 reference

Primary episodic ataxias: diagnosis, pathogenesis and treatment

21 January 2018

1 reference

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus

21 January 2018

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A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia

21 January 2018

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Vestibulocerebellar ataxia. A newly defined hereditary syndrome with periodic manifestations

21 January 2018

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Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias

21 January 2018

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Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia

21 January 2018

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Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures

21 January 2018

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A new episodic ataxia syndrome with linkage to chromosome 19q13.

21 January 2018

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Benign paroxysmal tonic upgaze of childhood

21 January 2018

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Episodic dystonic spasm of the bilateral edge of the tongue during a coma following anoxic encephalopathy.

21 January 2018

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Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.23765

1 reference

31 July 2017

1 reference

PubMed ID

21626559