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Article

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

1 Oct 1997

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9382100
DOI: 10.1086/514877

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Related research

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Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16PMID 9382100Read ↗

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis SyndromeSemantic proximity Read ↗

Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromesSemantic proximity Read ↗

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

Paroxysmal kinesigenic choreoathetosis: evidence of linkage to the pericentromeric region of chromosome 16 in four Chinese families.Semantic proximity Read ↗

Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation.Semantic proximity Read ↗

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.Semantic proximity Read ↗

Multiple phenotypic traits including developmental impairment in a Chinese family with infantile convulsion and choreoathetosis syndrome: a case study expanding the clinical spectrum of prrt2-related syndrome.Semantic proximity Read ↗

Idiopathic Epilepsy and Paroxysmal DyskinesiaSemantic proximity Read ↗

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 16Semantic proximity Read ↗

[PRRT2 gene-related paroxysmal disorders].Semantic proximity Read ↗

Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.Semantic proximity Read ↗

Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy.Semantic proximity Read ↗

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