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EPILEPSY, BENIGN NEONATAL, 2

Known as: Convulsions benign familial neonatal dominant form, BFNC2, CONVULSIONS, BENIGN FAMILIAL NEONATAL, 2 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal dominant inheritanceFocal Clonic SeizuresSeizures, afebrileSpheroid body myopathy

Broader (2)

Benign Familial ConvulsionBenign neonatal epilepsy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Anovel KCNQ 3 mutation in familial epilepsy with focal seizures and intellectual disability
Mutations in the KCNQ2 gene encoding for voltage-gated potassium channel subunits have been found in patients affected with early… 
2004
2004
Novel mutations in the KCNQ 2 gene link epilepsy to a dysfunction of the KCNQ 2-calmodulin interaction
M utations in the voltage gated potassium channels KCNQ2 (OMIM 602235) and KCNQ3 (OMIM 602232) are associated with an autosomal… 
Review
2001
Review
2001
[Idiopathic epileptic syndromes of the newborn].
INTRODUCTION Seizures during the neonatal period are the characteristic clinical expression of dysfunction of the nervous system… 
Review
1999
Review
1999
Chapter 56 – Overview
Highly Cited
1990
Highly Cited
1990
[Benign familial neonatal seizures].
  • H. Siemes
  • Monatsschrift Kinderheilkunde : Organ der…
  • 1990
  • Corpus ID: 42999183
Benign familial neonatal seizures are a rare cause of newborn seizures which can be easily detected by the family history because… 
1985
1985
The syndrome of benign familial neonatal seizures.
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