Early-onset absence epilepsy and paroxysmal dyskinesia (Q44169583)

30 November 2017

title

Early-onset absence epilepsy and paroxysmal dyskinesia (English)

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Kailash Phatechand Bhatia

30 November 2017

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5

object named as

Kailash P Bhatia

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1

Renzo Guerrini

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Bernardo Dalla Bernardina

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8

object named as

Bernardo Dalla Bernardina

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30 November 2017

author name string

Rocio Sanchez-Carpintero

2

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Thierry Deonna

3

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Margherita Santucci

4

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Teresa Moreno

6

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Lucio Parmeggiani

7

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publication date

1 October 2002

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volume

43

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issue

10

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30 November 2017

page(s)

1224-1229

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Paroxysmal choreoathetosis. Report of Chinese cases

30 November 2017

cites work

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https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes

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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Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Epilepsy with typical absence seizures with onset during the first year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

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

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Benign paroxysmal tonic upgaze of childhood

21 January 2018

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https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Benign paroxysmal tonic upgaze of childhood--a new syndrome

21 January 2018

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https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

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

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

21 January 2018

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https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Mutation of the Ca2 channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

21 January 2018

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Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16

21 January 2018

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Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

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

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

Paroxysmal movement disorders and epilepsy: links across the channel

21 January 2018

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https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

[Benign familial infantile convulsions]

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1528-1157.2002.13802.X

10.1046/J.1528-1157.2002.13802.X

21 January 2018

Identifiers

DOI

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30 November 2017

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