These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
149 related articles for article (PubMed ID: 35853415)
21. Generation of an induced pluripotent stem cell (iPSC) line from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Leu328Val) mutation. Schwarz N; Uysal B; Rosa F; Löffler H; Mau-Holzmann UA; Liebau S; Lerche H Stem Cell Res; 2018 Dec; 33():6-9. PubMed ID: 30292882 [TBL] [Abstract][Full Text] [Related]
22. De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders. Vaher U; Nõukas M; Nikopensius T; Kals M; Annilo T; Nelis M; Ounap K; Reimand T; Talvik I; Ilves P; Piirsoo A; Seppet E; Metspalu A; Talvik T J Child Neurol; 2014 Dec; 29(12):NP202-6. PubMed ID: 24352161 [TBL] [Abstract][Full Text] [Related]
27. Severe bone loss and multiple fractures in SCN8A-related epileptic encephalopathy. Rolvien T; Butscheidt S; Jeschke A; Neu A; Denecke J; Kubisch C; Meisler MH; Pueschel K; Barvencik F; Yorgan T; Oheim R; Schinke T; Amling M Bone; 2017 Oct; 103():136-143. PubMed ID: 28676440 [TBL] [Abstract][Full Text] [Related]
28. Genetic and clinical features of SCN8A developmental and epileptic encephalopathy. Kim HJ; Yang D; Kim SH; Kim B; Kim HD; Lee JS; Choi JR; Lee ST; Kang HC Epilepsy Res; 2019 Dec; 158():106222. PubMed ID: 31675620 [TBL] [Abstract][Full Text] [Related]
31. SCN8A Epileptic Encephalopathy: Detection of Fetal Seizures Guides Multidisciplinary Approach to Diagnosis and Treatment. McNally MA; Johnson J; Huisman TA; Poretti A; Baranano KW; Baschat AA; Stafstrom CE Pediatr Neurol; 2016 Nov; 64():87-91. PubMed ID: 27659738 [TBL] [Abstract][Full Text] [Related]
32. A Novel Inherited Mutation of Han JY; Jang JH; Lee IG; Shin S; Park J Ann Clin Lab Sci; 2017 Nov; 47(6):747-753. PubMed ID: 29263050 [TBL] [Abstract][Full Text] [Related]
34. Mutations in SCN3A cause early infantile epileptic encephalopathy. Zaman T; Helbig I; Božović IB; DeBrosse SD; Bergqvist AC; Wallis K; Medne L; Maver A; Peterlin B; Helbig KL; Zhang X; Goldberg EM Ann Neurol; 2018 Apr; 83(4):703-717. PubMed ID: 29466837 [TBL] [Abstract][Full Text] [Related]
35. Phenotypic and genetic spectrum in Chinese children with SCN8A-related disorders. Hu C; Luo T; Wang Y Seizure; 2022 Feb; 95():38-49. PubMed ID: 34979445 [TBL] [Abstract][Full Text] [Related]
36. Astrocyte reactivity in a mouse model of SCN8A epileptic encephalopathy. Thompson JA; Miralles RM; Wengert ER; Wagley PK; Yu W; Wenker IC; Patel MK Epilepsia Open; 2022 Jun; 7(2):280-292. PubMed ID: 34826216 [TBL] [Abstract][Full Text] [Related]
37. Neonatal tremor episodes and hyperekplexia-like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy. Pons L; Lesca G; Sanlaville D; Chatron N; Labalme A; Manel V; Arzimanoglou A; de Bellescize J; Lion-François L Epileptic Disord; 2018 Aug; 20(4):289-294. PubMed ID: 30078772 [TBL] [Abstract][Full Text] [Related]
38. Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach. Boerma RS; Braun KP; van den Broek MP; van Berkestijn FM; Swinkels ME; Hagebeuk EO; Lindhout D; van Kempen M; Boon M; Nicolai J; de Kovel CG; Brilstra EH; Koeleman BP Neurotherapeutics; 2016 Jan; 13(1):192-7. PubMed ID: 26252990 [TBL] [Abstract][Full Text] [Related]