Classification of familial neonatal convulsions
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Benign familial neonatal convulsions linked to genetic markers on chromosome 20;Leppert;Nature,1989
2. Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity;Ryan;Ann Neurol,1991
3. Benign familial neonatal convulsions: clinical features of the propositus and comparison with the previously reported cases;Wakai;Acta Paediatr Jpn,1991
4. Infantile spasms in one member of a family with benign familial neonatal convulsions;Mori;Epilepsia,1993
5. Benign familial neonatal convulsions: generalised epilepsy?;Aso;Pediatr Neurol,1992
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1. Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions;Child Neurology Open;2017-01-01
2. Severe Neonatal Epileptic Encephalopathy and KCNQ2 Mutation: Neuropathological Substrate?;Frontiers in Pediatrics;2014-12-19
3. Molecular bases and clinical spectrum of early infantile epileptic encephalopathies;European Journal of Medical Genetics;2012-05
4. KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy;Annals of Neurology;2012-01
5. Benign familial neonatal convulsions: Always benign?;Epilepsy Research;2007-03
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