Results 141 to 150 of about 8,423 (186)

Hippocampal malformation in Dravet syndrome. [PDF]

Epilepsia
Okutoyi NE, Maru V, Nauen DW.
europepmc   +1 more source

Disrupted inhibitory interneuron development in SCN1A Dravet syndrome revealed by patient-derived subpallial organoids. [PDF]

Epilepsia
Mattei C, Mao M, Byars S, Syazwan EM, Oliva M, Karle TJ, Richards K, Scheffer IE, Petrou S, Maljevic S.   +9 more
europepmc   +1 more source

Early-Onset and Syndromic Pediatric Epilepsy in Kazakhstan: Clinical, Molecular, and Phenotypic Spectrum. [PDF]

J Clin Med
Bayanova M, Nazarova L, Zhakupov A, Malik D, Gabdulkayum A, Mirmanova Z, Satvaldina N, Rakhimova S, Akilzhanova A, Yerezhepov D, Bolatov A.   +10 more
europepmc   +1 more source

STAT3 signaling is associated with neuroimmune dysregulation in a Dravet syndrome model and pediatric drug-resistant epilepsy. [PDF]

Front Neurosci
Zhang Q, Wang JC, Zhao HQ, Wang J, Xu BJ, Zou LP.   +5 more
europepmc   +1 more source

Long-lasting remodeling of astrocytes in an Scna1^+/- mouse model of Dravet syndrome. [PDF]

Epilepsia
Genin A, Janvier A, Moujellil-Legagneur T, Blaquière M, Chaussy A, Privé R, Duprat F, Mantegazza M, Audinat E, Marchi N, Cresto N.   +10 more
europepmc   +1 more source

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

Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies. [PDF]

Epilepsia
Gverdtsiteli S, Ortiz S, Brünger T, Furia F, Barba C, Bjørg-Hammer T, Borggraefe I, Caraballo R, Cirak S, Espeche A, Fazeli W, Guerrini R, Juanes M, Kassahn K, Kinali M, Krämer J, Kröll J, Herrero MCM, Oegema R, Ounap K, Peñuela O, Platzer K, Prasad AN, Pujol A, Reinson K, Represa A, Roza E, Valenzuela GR, Rodríguez-Palmero A, Sallevelt S, Sanchez-Albiusa MI, Scheffer IE, Smid C, Stafstrom CE, Stattin EL, Suarez JR, Syrbe S, Valente KD, Wagner M, Wortmann S, Gardella E, Lal D, Brunklaus A, Møller RS.   +43 more
europepmc   +1 more source

Genetic Diagnosis in Epilepsy: Implications for Clinical Management. [PDF]

Curr Neurol Neurosci Rep
Schatz KS, Lammert DB, Habela CW.
europepmc   +1 more source

Natural antisense transcript Nat9a suppresses Scn9a (Na_V1.7) expression in parvalbumin-positive proprioceptive and inhibitory neurons. [PDF]

Sci Rep
Li S, Santana-Varela S, Mikaeili H, Habib AM, Patel J, Tian N, Okorokov AL, Cox JJ.   +7 more
europepmc   +1 more source

Advancing Disease Modification in Dravet Syndrome. [PDF]

Epilepsy Curr
Fine AL.
europepmc   +1 more source