Acute encephalopathy in children with Dravet syndrome. (Q51173083)

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16 January 2020

title

Acute encephalopathy in children with Dravet syndrome (English)

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16 January 2020

2

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16 January 2020

Tohru Okanishi

5

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16 January 2020

Shinji Saitoh

14

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16 January 2020

Iori Ohmori

10

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16 January 2020

author name string

Akihisa Okumura

1

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16 January 2020

George Imataka

3

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16 January 2020

Manabu Tanaka

4

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16 January 2020

Tetsuo Kubota

6

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16 January 2020

Akira Sudo

7

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16 January 2020

Jun Tohyama

8

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16 January 2020

Megumi Tsuji

9

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16 January 2020

Misako Naiki

11

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16 January 2020

Ayako Hiraiwa-Sofue

12

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16 January 2020

Hitoshi Sato

13

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16 January 2020

Toshiaki Shimizu

15

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16 January 2020

publication date

16 November 2011

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16 January 2020

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16 January 2020

volume

53

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16 January 2020

issue

1

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16 January 2020

page(s)

79-86

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

16 January 2020

cites work

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Unusual consequences of status epilepticus in Dravet syndrome.

21 January 2018

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

21 January 2018

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

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Molecular genetics of Dravet syndrome

21 January 2018

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Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females

21 January 2018

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Genetic seizure susceptibility underlying acute encephalopathies in childhood

21 January 2018

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Protocadherin 19 mutations in girls with infantile-onset epilepsy

21 January 2018

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Acute necrotizing encephalopathy of childhood: a novel form of acute encephalopathy prevalent in Japan and Taiwan

21 January 2018

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Acute encephalopathy associated with influenza and other viral infections

21 January 2018

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Encephalitis and encephalopathy associated with an influenza epidemic in Japan

21 January 2018

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Acute encephalopathy with inflammation-mediated status epilepticus

21 January 2018

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Prognostic factors in influenza-associated encephalopathy.

21 January 2018

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Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation

21 January 2018

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Severe myoclonic epilepsy in infants--a review based on the Tokyo Women's Medical University series of 84 cases

21 January 2018

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Differences of clinical manifestations according to the patterns of brain lesions in acute encephalopathy with reduced diffusion in the bilateral hemispheres

21 January 2018

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Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome.

21 January 2018

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Hippocampal sclerosis in severe myoclonic epilepsy in infancy: a retrospective MRI study

21 January 2018

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Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

21 January 2018

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Two newly proposed infectious encephalitis/encephalopathy syndromes

21 January 2018

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Diffusion MRI abnormalities after prolonged febrile seizures with encephalopathy.

21 January 2018

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Acute encephalopathy with a truncation mutation in the SCN1A gene: a case report.

21 January 2018

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Acute Encephalopathy in a Patient with Dravet Syndrome

21 January 2018

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Differences in clinical manifestations of influenza-associated encephalopathy by age.

21 January 2018

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