(Q53663086)

17 May 2018

title

Benign familial infantile seizures: further delineation of the syndrome. (English)

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17 May 2018

author name string

Roberto Horacio Caraballo

1

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17 May 2018

Ricardo Oscar Cersósimo

2

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17 May 2018

Hernan Amartino

3

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17 May 2018

Pierre Szepetowski

4

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17 May 2018

Natalio Fejerman

5

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17 May 2018

publication date

1 September 2002

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17 May 2018

Journal of Child Neurology

published in

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17 May 2018

volume

17

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17 May 2018

issue

9

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17 May 2018

page(s)

696-699

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17 May 2018

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

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Benign infantile epilepsy with autosomal dominant inheritance

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Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome

21 January 2018

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Benign familial infantile convulsions: report of a UK family and confirmation of genetic heterogeneity

21 January 2018

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Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity

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

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

21 January 2018

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Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies

21 January 2018

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

21 January 2018

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Validation of a questionnaire for clinical seizure diagnosis

21 January 2018

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Early recognition of benign partial epilepsy in infancy.

21 January 2018

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An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

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A potassium channel mutation in neonatal human epilepsy

21 January 2018

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

21 January 2018

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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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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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21 January 2018

Identifiers

DOI

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17 May 2018

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17 May 2018