You are on the new improved site. You can view the old site in view-only mode here until June 27, 2026

Filter Results

Search all journals

Enter search terms…

Advanced search

/

About

About Sage
About Sage Journals
Privacy Policy
Terms of Use
Contact Us
Help

Information for

Authors
Editors
Librarians
Researchers
Reviewers
Frequently asked questions

Copyright © 2026 by Sage Publications.京ICP备09090397号-11

Search results

Search results page

Articles (29)

Journals (0)

1-10 of 29 results for infantile convulsions

Sort by:

Relevance

Select all

Select all

Sort by:

Relevance

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

Retricted access

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

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

Retricted access

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

Select article: Benign Familial Infantile Convulsions: Phenotypic Variability in a Family

Retricted access

Other

First published 2005-06

Benign Familial Infantile Convulsions: Phenotypic Variability in a Family

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

Journal of Child Neurology

Select article: Benign Familial Infantile Convulsions: Phenotypic Variability in a Family

Retricted access

Other

First published 2005-06

Benign Familial Infantile Convulsions: Phenotypic Variability in a Family

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

Journal of Child Neurology

Select article: Three siblings with self-limited familial infantile epilepsy with PRRT2 mutation: A case series

Open access

Case report

First published 2024

Three siblings with self-limited familial infantile epilepsy with PRRT2 mutation: A case series

Naoto Iwanami, Shigeru Nagaki, Aki Gen [...]

Sage Open Medical Case Reports

Select article: Bilateral Optic Nerve Atrophy in a Child,with Positive Wassermann Reaction and History of Infantile Convulsions

Free access

Research article

First published 1917-4

Bilateral Optic Nerve Atrophy in a Child,with Positive Wassermann Reaction and History of Infantile Convulsions

F. Parkes Weber

Journal of the Royal Society of Medicine

Select article: Benign Familial Infantile Seizures: Further Delineation of the Syndrome

Retricted access

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

Select article: Benign Convulsions With Mild Gastroenteritis: Is It Associated With Sodium Channel Gene SCN1A Mutation?

Retricted access

Other

First published 2010-12

Benign Convulsions With Mild Gastroenteritis: Is It Associated With Sodium Channel Gene SCN1A Mutation?

Wen-Chin Weng, Shinichi Hirose, Wang-Tso Lee

Journal of Child Neurology

Select article: Possessed by Evil Spirits

Retricted access

Research article

First published 2014-7

Possessed by Evil Spirits

Michael Obladen

Journal of Child Neurology

Select article: Topical Review: Benign Idiopathic Partial Epilepsies in Infancy

Retricted access

Review article

First published 2001-12

Topical Review: Benign Idiopathic Partial Epilepsies in Infancy

Giuseppe Capovilla, Federico Vigevano

Journal of Child Neurology

1
2
3
10 / page

Article type

Publication date

Subjects

Access