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Research article

First published 2007-12

Mutation Analysis of WASF2 and GALE Genes in One Chinese Family with Benign Familial Infantile Convulsions with a Novel Locus

Zi Xiaohong, Mutasem Abuhamed, Wang Ya-qin

Journal of Investigative Medicine

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Other

First published 2005-06

Benign Familial Infantile Convulsions: Phenotypic Variability in a Family

Ercan Demir, Güzide Turanl, Dilek Yalnzoğlu [...]

Journal of Child Neurology

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Other

First published 2005-06

Benign Familial Infantile Convulsions: Phenotypic Variability in a Family

Ercan Demir, Güzide Turanlτ, Dilek Yalnτzoğlu [...]

Journal of Child Neurology

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Research article

First published 2015-9

Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome

L. M. Zhang, Y. An, G. Pan [...]

Journal of Child Neurology

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Other

First published 2002-09

Benign Familial Infantile Seizures: Further Delineation of the Syndrome

Roberto Horacio Caraballo, Ricardo Oscar Cersósimo, Heman Amartino [...]

Journal of Child Neurology

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Other

First published 1996-05

Evidence of a Third Locus for Benign Familial Convulsions

Tracey B. Lewis, Michael I. Shevell, Eva Andermann [...]

Journal of Child Neurology

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Review article

First published 2001-12

Topical Review: Benign Idiopathic Partial Epilepsies in Infancy

Giuseppe Capovilla, Federico Vigevano

Journal of Child Neurology

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Research article

First published 1985-1

The Benign Infantile Epilepsies with Evoked Spikes

Pasquale DeMarco

Clinical EEG and Neuroscience

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Research article

First published 2026

A Case of Atypical Presentation of Paroxysmal Movement Disorder,Contributed to PRRT2 Gene Variant

Mariah Pace, Doriette Soler

Journal of Child Neurology

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Research article

First published 1996-5

Familial Hemiplegic Migraine: A Clinical Comparison of Families Linked and Unlinked to Chromosome 19

GM Terwindt, RA Ophoff, J Haan [...]

Cephalalgia

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