(Q28186159)

1

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C Marini

2

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S Petrou

3

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L A Harkin

4

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D N Bowser

5

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R G Panchal

6

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D A Williams

7

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G R Sutherland

8

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J C Mulley

9

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I E Scheffer

10

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S F Berkovic

Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984.

11

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language of work or name

English

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publication date

May 2001

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published in

Nature Genetics

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volume

28

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issue

1

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page(s)

49-52

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cites work

1 reference

7 January 2021

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

1 reference

7 January 2021

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

7 January 2021

A potassium channel mutation in neonatal human epilepsy

1 reference

7 January 2021

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1 reference

7 January 2021

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

1 reference

7 January 2021

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

7 January 2021

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

1 reference

7 January 2021

Genetics of the epilepsies

1 reference

7 January 2021

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

1 reference

7 January 2021

Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy

1 reference

7 January 2021

Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.

1 reference

7 January 2021

Possible association between childhood absence epilepsy and the gene encoding GABRB3

1 reference

7 January 2021

Concordance of clinical forms of epilepsy in families with several affected members. Italian League Against Epilepsy Genetic Collaborative Group

1 reference

7 January 2021

Functional and molecular distinction between recombinant rat GABAA receptor subtypes by Zn2+

1 reference

7 January 2021

Febrile seizures: treatment and prognosis

1 reference

7 January 2021

GABA and epileptogenesis

1 reference

7 January 2021

Thalamocortical oscillations in the sleeping and aroused brain

1 reference

7 January 2021

Developmental changes in human gamma-aminobutyric acidA receptor subunit composition.

1 reference

7 January 2021

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

1 reference

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

7 January 2021

Consolidated OpenCitations Corpus – April 2017

Identifiers

0 references

1 reference

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11326275

1 reference

Consolidated OpenCitations Corpus – April 2017