KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy. (Q42501055)

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21 January 2020

title

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy (English)

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21 January 2020

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21 January 2020

Arvid Suls

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21 January 2020

Anna C Jansen

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21 January 2020

Sarah E Heron

19

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Samuel Berkovic

21

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Ingrid Scheffer

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21 January 2020

author name string

Dominique Audenaert

4

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21 January 2020

Tine Deconinck

5

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21 January 2020

Lieve R F Claes

6

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Liesbet Deprez

7

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Katrien Smets

8

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21 January 2020

Dimitrina Hristova

9

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Iglika Yordanova

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Albena Jordanova

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Berten Ceulemans

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Danièle Hasaerts

14

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21 January 2020

Filip Roelens

15

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21 January 2020

Lieven Lagae

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21 January 2020

Simone Yendle

17

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21 January 2020

Thorsten Stanley

18

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21 January 2020

John C Mulley

20

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Peter de Jonghe

23

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21 January 2020

Sarah Weckhuysen

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21 January 2020

publication date

1 January 2012

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21 January 2020

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21 January 2020

volume

71

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21 January 2020

issue

1

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21 January 2020

page(s)

15-25

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Electroclinical signs of benign neonatal familial convulsions

21 January 2020

cites work

1 reference

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

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

21 January 2018

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Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures

21 January 2018

1 reference

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

21 January 2018

1 reference

Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2

21 January 2018

1 reference

A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation

21 January 2018

1 reference

Benign familial neonatal convulsions: always benign?

21 January 2018

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Neonatal seizures with tonic clonic sequences and poor developmental outcome

21 January 2018

1 reference

Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion.

21 January 2018

1 reference

Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel

21 January 2018

1 reference

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

21 January 2018

1 reference

Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations

21 January 2018

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Excitotoxicity in neonatal hypoxia

21 January 2018

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Patterns of neonatal hypoxic-ischaemic brain injury

21 January 2018

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Patterns of brain injury in term neonatal encephalopathy.

21 January 2018

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Cellular expression of ionotropic glutamate receptor subunits on specific striatal neuron types and its implication for striatal vulnerability in glutamate receptor-mediated excitotoxicity

21 January 2018

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Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.

21 January 2018

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Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs

21 January 2018

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