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Results for
""Epilepsies, Myoclonic""[mesh_terms]

120 Results

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Treatment of Dravet Syndrome.

Elaine C Wirrell

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2017;43 Suppl 3():S13-8

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The ketogenic diet in Dravet syndrome.

Robyn Blackford, Linda Laux

Journal of child neurology 2014;28(8):1041-4

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Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies.

Ingrid Scheffer, Simona Balestrini, Renzo Guerrini

The Lancet. Neurology 2025;24(4):348-360

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"Severe myoclonic epilepsy in infancy". Relevance for the clinician of severe epilepsy starting in infancy.

Berten Ceulemans, Patrick Cras

Acta neurologica Belgica 2005;104(3):95-9

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Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.

Zhi-dong Cen, Fei Xie, Jian-feng Xiao, Wei Luo

Seizure 2016;34():83-9

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Genetic epileptic encephalopathies: is all written into the DNA?

Pasquale Striano, Peter de Jonghe, Federico Zara

Epilepsia 2014;54 Suppl 8():22-6

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Childhood epilepsy.

Ramshekhar N Menon, J Helen Cross

Lancet (London, England) 2025;406(10503):636-649

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An Update on Stiripentol Mechanisms of Action: A Narrative Review.

Marie-Emmanuelle Le Guern, Elaine C Wirrell, Alexandre Bacq, Antoine Depaulis, Vincent Castagné, Marc Verleye

Advances in therapy 2024;41(4):1351-1371

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Response to lacosamide monotherapy in a patient with medically refractory Jeavons syndrome: a case report and review of the literature.

Ifrah Zawar, Linda Franic, Elia Pestana Knight

Epileptic disorders : international epilepsy journal with videotape 2021;22(5):643-647

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Dravet syndrome: Treatment options and management of prolonged seizures.

J Helen Cross, Roberto H Caraballo, Rima Nabbout, Federico Vigevano, Renzo Guerrini, Lieven Lagae

Epilepsia 2020;60 Suppl 3():S39-S48

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Dravet Syndrome: Past, Present, and Future.

Yi-Hsuan Liu, Cheng-Yen Kuo, I-Ching Chou, Ting-Rong Hsu, Kuang-Lin Lin

Acta neurologica Taiwanica 2025;34(3):125-132

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Cannabidiol reveals a disruptive strategy for 21st century epilepsy drug discovery.

Aaron Del Pozo, Melissa Barker-Haliski

Experimental neurology 2022;360():114288

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The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy.

Bernardo Dalla Bernardina, Roberto Caraballo, Francesca Darra, Gabriela Reyes, Marisa Armeno, Araceli Cresta, Graciela Mestre

Seizure 2018;51():1-5

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Current therapeutic procedures in Dravet syndrome.

Catherine Chiron

Developmental medicine and child neurology 2011;53 Suppl 2():16-8

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Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome).

I E Scheffer, J C Mulley, S F Berkovic, R Wallace

Brain & development 2002;23(7):732-5

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Results: 1 – 15 / 120

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Results for ""Epilepsies, Myoclonic""[mesh_terms]

Treatment of Dravet Syndrome.

The ketogenic diet in Dravet syndrome.

Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies.

"Severe myoclonic epilepsy in infancy". Relevance for the clinician of severe epilepsy starting in infancy.

Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.

Genetic epileptic encephalopathies: is all written into the DNA?

Childhood epilepsy.

An Update on Stiripentol Mechanisms of Action: A Narrative Review.

Response to lacosamide monotherapy in a patient with medically refractory Jeavons syndrome: a case report and review of the literature.

Dravet syndrome: Treatment options and management of prolonged seizures.

Dravet Syndrome: Past, Present, and Future.

Cannabidiol reveals a disruptive strategy for 21st century epilepsy drug discovery.

The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy.

Current therapeutic procedures in Dravet syndrome.

Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome).

Results for
""Epilepsies, Myoclonic""[mesh_terms]