Hippocampal sclerosis in severe myoclonic epilepsy in infancy: a retrospective MRI study. - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q48909939

about

Neuroimaging and neuropathology of Dravet syndrome.Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction.Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.Dravet syndrome and SCN1A gene mutation related-epilepsies: cognitive impairment and its determinants.Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.Co-occurring malformations of cortical development and SCN1A gene mutations.Dravet syndrome--considerable delay in making the diagnosis.Dravet syndrome Authors' response to correspondence on "mesial temporal sclerosis in a cohort of children with SCN1A gene mutation".Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.Mesial temporal sclerosis in children with SCN1A mutation.Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.Atypical propositional language organization in prenatal and early-acquired temporal lobe lesions.Mesial temporal sclerosis in a cohort of children with SCN1A gene mutation.A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009.Acute encephalopathy in children with Dravet syndrome.

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P2860

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

http://www.wikidata.org/entity/Q48909939

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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name

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

@en

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

@nl

type

label

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

@en

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

@nl

prefLabel

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

@en

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

@nl

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

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Andras Fogarasi

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Eva Paraicz

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Jozsef Janszky

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Judit Jerney

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Magdolna Neuwirth

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Maria Kassay

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Marta Hegyi

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Peter Barsi

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Zsuzsanna Siegler

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P2860

Childhood-onset epilepsy with and without preceding febrile seizures

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation

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)

Hippocampal malrotation with normal corpus callosum: a new entity?

Do prolonged febrile seizures produce medial temporal sclerosis? Hypotheses, MRI evidence and unanswered questions.

From swelling to sclerosis: acute change in mesial hippocampus after prolonged febrile seizure.

Hippocampal sclerosis revisited.

Prolonged febrile seizures in the immature rat model enhance hippocampal excitability long term.

A magnetic resonance study of complicated early childhood convulsion.

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704-708

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