Results 151 to 160 of about 537,666 (200)

Identification of Copy Number Variations in Familial Hemiplegic Migraine Genes in Suspected Hemiplegic Migraine Patients. [PDF]

Biomedicines
Zielke T, Sutherland HG, Maksemous N, Smith RA, Griffiths LR.   +4 more
europepmc   +1 more source

Astrocytes in Genetic Epilepsies: Supporting Actor or Key Player? [PDF]

J Neurosci Res
Lange J, Zhao E, O'Connell E, Gillham O, McTague A.   +4 more
europepmc   +1 more source

Epilepsy-Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties. [PDF]

Ann Clin Transl Neurol
Liebovitz LN, Thompson CH, Laux LC, George AL.   +3 more
europepmc   +1 more source

Gene variants in periventricular nodular heterotopia. [PDF]

Acta Epileptol
Song J, Sun X, Zhang C.
europepmc   +1 more source

Urine-Derived iPSC Neurospheres Uncover Proteomic Correlates of Clinical Severity in Dravet Syndrome. [PDF]

J Neurochem
Martins M, Nugue G, Aguiar A, Souza LRQ, Abrantes PV, Trajano JR, Stelling M, Junqueira M, Rehen S, Guimarães MZP.   +9 more
europepmc   +1 more source

Genetic-Epigenetic Interplay in Epilepsy: Pathways, Biomarkers, and Epigenome-Targeted Therapies. [PDF]

Epigenomes
Zaruha AG, Codreanu P, Coman MC, Novac Ii MA, Duță-Ion SG, Jugănaru IR, Hotinceanu IA, Dan A, Burtavel LM, Eftenoiu AE, Bârcă D, Ionescu A, Paraschiv C, Rădoi VE.   +13 more
europepmc   +1 more source

Dravet Syndrome Associated With a CSNK2B-Related Neurodevelopmental Disorder. [PDF]

Cureus
Yeboah AO, Tyshkov CD, Ghosh S.
europepmc   +1 more source

Correction: Evolution, hibernation, and inactivation of voltage-gated Na channels. [PDF]

J Gen Physiol
Willis JS.
europepmc   +1 more source

Development of Novel Small-Molecule Targeting SCN1A-Associated Severe Myoclonic Epilepsy of Infancy. [PDF]

J Med Chem
Kim DG, Hwang KS, Ahn SH, Kim SS, Son Y, Park SB, Jung WH, Shin DS, Cho SH, Choi BW, Kim P, Heo Y, Kim M, Yang JY, Lee KR, Lee HA, Kim J, Kang HC, Kim KY, Bae MA, Ahn JH.   +20 more
europepmc   +1 more source

A case of Dravet syndrome with a novel SCN1A gross deletion involving the promoter region. [PDF]

Hum Genome Var
Nakahara Sakamoto E, Shimada S, Yamaguchi T, Ishida T, Imai K, Eguchi H, Okazaki Y, Arai M.   +7 more
europepmc   +1 more source