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Familial benign neonatal epilepsy
Known as:
Benign Neonatal-Infantile Epilepsy
, Familial Benign Neonatal Convulsions
, BFIS1
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National Institutes of Health
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Related topics
Related topics
6 relations
Autosomal dominant inheritance
Benign Neonatal Epilepsy, Nonfamilial
Cyanosis
SEIZURES, BENIGN FAMILIAL INFANTILE, 3
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Broader (1)
Benign neonatal epilepsy
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Current trends in the treatment of infantile spasms
C. Tsao
Neuropsychiatric Disease and Treatment
2009
Corpus ID: 79158
Infantile spasms are an epilepsy syndrome with distinctive features, including age onset during infancy, characteristic epileptic…
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Highly Cited
2006
Highly Cited
2006
Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain
J. Geiger
,
Y. Weber
,
B. Landwehrmeyer
,
C. Sommer
,
H. Lerche
Neuroscience Letters
2006
Corpus ID: 23034230
Highly Cited
2004
Highly Cited
2004
De novo KCNQ2 mutations in patients with benign neonatal seizures
L. Claes
,
B. Ceulemans
,
+8 authors
P. de Jonghe
Neurology
2004
Corpus ID: 23701482
Benign familial neonatal convulsions (BFNC) are characterized by unprovoked seizures during the first weeks of life with…
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Highly Cited
2002
Highly Cited
2002
New human sodium/glucose cotransporter gene (KST1): identification, characterization, and mutation analysis in ICCA (infantile convulsions and choreoathetosis) and BFIC (benign familial infantile…
P. Roll
,
A. Massacrier
,
S. Pereira
,
A. Robaglia-Schlupp
,
P. Cau
,
P. Szepetowski
Gene
2002
Corpus ID: 32052004
Highly Cited
2000
Highly Cited
2000
Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor
E. D. Giudice
,
G. Coppola
,
G. Scuccimarra
,
G. Cirillo
,
G. Bellini
,
A. Pascotto
European Journal of Human Genetics
2000
Corpus ID: 22866397
Benign familial neonatal convulsions (BFNC) is a rare autosomal inherited epilepsy. We studied the KCNQ2 coding region in a large…
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2000
2000
Pathophysiology of KCNQ Channels: Neonatal Epilepsy and Progressive Deafness
T. Jentsch
,
B. Schroeder
,
C. Kubisch
,
Thomas Friedrich
,
V. Stein
Epilepsia
2000
Corpus ID: 11646025
Over the past 10 years, an increasing number of inherited diseases were shown to be due to mutations in ion channels. Given the…
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1994
1994
A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)
C. Beck
,
B. Moulard
,
+5 authors
A. Malafosse
Neurobiology of Disease
1994
Corpus ID: 19382141
Benign Familial Neonatal Convulsions (BFNC) is an epileptic disorder with an autosomal dominant mode of transmission. It has been…
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1992
1992
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20
A. Malafosse
,
M. Leboyer
,
+12 authors
J. Mallet
Human Genetics
1992
Corpus ID: 19192190
SummaryBenign familial neonatal convulsions (BFNC) is an idiopathic form of epilepsy beginning within the first six months of…
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1988
1988
The effect of feeding four different formulae on stool weights in prolonged dehydrating infantile gastroenteritis.
Rashid Rajah
,
John M. Pettifor
,
+4 authors
Harry Stein
Journal of Pediatric Gastroenterology and…
1988
Corpus ID: 25723546
Prolonged diarrhea following an acute episode of dehydrating gastroenteritis in infants is often treated by the empirical removal…
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Highly Cited
1987
Highly Cited
1987
Prolonged exclusive breast feeding and heredity as determinants in infantile atopy.
E. Savilahti
,
V. Tainio
,
L. Salmenperä
,
M. Siimes
,
J. Perheentupa
Archives of Disease in Childhood
1987
Corpus ID: 12787665
We followed 183 infants for two years, 31 of whom were breast fed less than three and a half months (median 70 days; short breast…
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