(Q54600675)

1 June 2018

title

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study. (English)

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1 June 2018

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1

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1 June 2018

Jacinta M McMahon

Jacinta M McMahon

3

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Deepak Gill

Deepak S Gill

7

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Sameer M Zuberi

5

Sameer M Zuberi

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1 June 2018

Ingrid Scheffer

10

Ingrid E Scheffer

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author name string

Louise Harkin

2

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1 June 2018

James T Pelekanos

4

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1 June 2018

Elaine C Wirrell

6

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1 June 2018

Xenia Iona

8

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1 June 2018

John C Mulley

9

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1 June 2018

publication date

1 June 2006

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1 June 2018

published in

Lancet Neurology

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1 June 2018

volume

5

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1 June 2018

page(s)

488-492

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1 June 2018

issue

6

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1 June 2018

Neurological complications of pertussis inoculation

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A new method for active surveillance of adverse events from diphtheria/tetanus/pertussis and measles/mumps/rubella vaccines

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Acute encephalopathy and chronic neurological damage after pertussis vaccine

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7 January 2021

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

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7 January 2021

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

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De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

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Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.

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Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

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Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures

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Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB)

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SCN1A mutations and epilepsy

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From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

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Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity

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Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy

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7 January 2021

Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.

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A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline

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Identifiers

DOI

1 reference

1 June 2018

PubMed ID

16713920

1 reference

1 June 2018