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Publication : epilepsia (series 4) Publisher : wiley-blackwell Subject : dravet syndrome Filter by : Subject
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Academic Journal

A systems medicine strategy to predict the efficacy of drugs for monogenic epilepsies.

Subjects: EPILEPSY; DRUG efficacy; THERAPEUTICS

  • Source: Epilepsia (Series 4); Dec2022, Vol. 63 Issue 12, p3125-3133, 9p

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Academic Journal

The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: A population-based study from 2004 to 2009.

Subjects: *CHILDHOOD epilepsy; *GENETIC mutation; *SODIUM channelsDENMARK

  • Source: Epilepsia (Series 4). Apr2015, Vol. 56 Issue 4, pe36-e39. 4p.

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Academic Journal

Dravet syndrome-From epileptic encephalopathy to channelopathy.

Subjects: *SYNDROMES; *GENETIC mutation; *GENETIC code

  • Source: Epilepsia (Series 4). Jul2014, Vol. 55 Issue 7, p979-984. 6p.

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Academic Journal

Co-occurring malformations of cortical development and SCN1A gene mutations.

Subjects: *HUMAN abnormalities; *GENETIC mutation; *GENES

  • Source: Epilepsia (Series 4). Jul2014, Vol. 55 Issue 7, p1009-1019. 11p.

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Academic Journal

Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.

Subjects: SODIUM channels; BRUGADA syndrome; GENETIC disorders

  • Source: Epilepsia (Series 4); Dec2019 Supplement 3, Vol. 60, pS2-S7, 6p

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Academic Journal

A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndrome.

Subjects: *CHILDHOOD epilepsy; *GENETIC mutation; *COGNITION disorders

  • Source: Epilepsia (Series 4). Dec2012, Vol. 53 Issue 12, pe200-e203. 4p.

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Academic Journal

Protective effect of the ketogenic diet in Scn1a mutant mice.

Subjects: *KETOGENIC diet; *GENETIC mutation; *LABORATORY mice

  • Source: Epilepsia (Series 4). Nov2011, Vol. 52 Issue 11, p2050-2056. 7p.

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Academic Journal

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.

Subjects: *PEOPLE with epilepsy; *GENETIC mutation; *NUCLEOTIDE sequence

  • Source: Epilepsia (Series 4). Jul2011, Vol. 52 Issue 7, p1251-1257. 7p.

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Academic Journal

A novel GABAergic dysfunction in human Dravet syndrome.

Subjects: DRAVET syndrome; GABAERGIC neurons; SPASMS

  • Source: Epilepsia (Series 4); Nov2018, Vol. 59 Issue 11, p2106-2117, 12p

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Academic Journal

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk.

Subjects: HEART beat; EPILEPSY risk factors; TREATMENT of epilepsy

  • Source: Epilepsia (Series 4); Jul2018, Vol. 59 Issue 7, p1372-1380, 9p

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  • 1-10 of  51 results for ""GENETIC mutation""