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Articles (31)

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1-10 of 31 results for Early infantile epileptic encephalopathy

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Select article: Novel STXBP1 Mutations in 2 Patients With Early Infantile Epileptic Encephalopathy

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Research article

First published 2015-4

Novel STXBP1 Mutations in 2 Patients With Early Infantile Epileptic Encephalopathy

Mafalda Sampaio, Ruben Rocha, Saskia Biskup [...]

Journal of Child Neurology

Select article: Hemispherectomy in Early Infantile Epileptic Encephalopathy

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Other

First published 2007-01

Hemispherectomy in Early Infantile Epileptic Encephalopathy

Lorie Hamiwka, Michael Duchowny, Israel Alfonso [...]

Journal of Child Neurology

Select article: Epilepsy Surgery for Early Infantile Epileptic Encephalopathy (Ohtahara Syndrome)

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Research article

First published 2013-12

Epilepsy Surgery for Early Infantile Epileptic Encephalopathy (Ohtahara Syndrome)

Saleem I. Malik, Carlos A. Galliani, Angel W. Hernandez [...]

Journal of Child Neurology

Select article: Biallelic SCN2A Gene Mutation Causing Early Infantile Epileptic Encephalopathy: Case Report and Review

Open access

Case report

First published 2019

Biallelic SCN2A Gene Mutation Causing Early Infantile Epileptic Encephalopathy: Case Report and Review

Shahad AlSaif, Muhammad Umair, Majid Alfadhel

Journal of Central Nervous System Disease

Select article: Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy

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Research article

First published 2016-3

Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy

Semra Gürsoy, Derya Erçal

Journal of Child Neurology

Select article: Clinical Evaluation and Diagnosis of Severe Epilepsy Syndromes of Early Childhood

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Research article

First published 2009-8

Clinical Evaluation and Diagnosis of Severe Epilepsy Syndromes of Early Childhood

Mary L. Zupanc

Journal of Child Neurology

Select article: Persistence of Suppression-Bursts in a Patient With Ohtahara Syndrome

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Other

First published 2007-5

Persistence of Suppression-Bursts in a Patient With Ohtahara Syndrome

Russell P. Saneto, Marcio Sotero de Menezes

Journal of Child Neurology

Select article: Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements

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Research article

First published 2021-2

Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements

Imane Abdelmoumen, Sandra Jimenez, Ignacio Valencia [...]

Journal of Child Neurology

Select article: De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy,Multiple Congenital Anomalies,and Movement Disorders

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Research article

First published 2014-12

De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy,Multiple Congenital Anomalies,and Movement Disorders

Ulvi Vaher, Margit Nõukas, Tiit Nikopensius [...]

Journal of Child Neurology

Select article: Infantile Spasms in Inborn Errors of Metabolism: Diagnostic and Therapeutic Considerations

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Research article

First published 2025

Infantile Spasms in Inborn Errors of Metabolism: Diagnostic and Therapeutic Considerations

Ersida Buraniqi, Hsuan-Tung Lee, Kuntal Sen [...]

Journal of Child Neurology

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