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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 36357057)

  • 1. Neuraxial block anesthetic technique in a patient with SCN8A encephalopathy: case report.
    Machado EGE; Bill IDRC; Ara Jo MMPDN; Neves JFNPD; Mau S GL; Marcos MFB; Ara Jo FP
    Braz J Anesthesiol; 2022; 72(6):826-828. PubMed ID: 36357057
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatostatin-Positive Interneurons Contribute to Seizures in
    Wengert ER; Miralles RM; Wedgwood KCA; Wagley PK; Strohm SM; Panchal PS; Idrissi AM; Wenker IC; Thompson JA; Gaykema RP; Patel MK
    J Neurosci; 2021 Nov; 41(44):9257-9273. PubMed ID: 34544834
    [No Abstract]   [Full Text] [Related]  

  • 3. Aberrant Sodium Channel Currents and Hyperexcitability of Medial Entorhinal Cortex Neurons in a Mouse Model of
    Ottolini M; Barker BS; Gaykema RP; Meisler MH; Patel MK
    J Neurosci; 2017 Aug; 37(32):7643-7655. PubMed ID: 28676574
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy.
    de Kovel CG; Meisler MH; Brilstra EH; van Berkestijn FM; van 't Slot R; van Lieshout S; Nijman IJ; O'Brien JE; Hammer MF; Estacion M; Waxman SG; Dib-Hajj SD; Koeleman BP
    Epilepsy Res; 2014 Nov; 108(9):1511-8. PubMed ID: 25239001
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prax330 reduces persistent and resurgent sodium channel currents and neuronal hyperexcitability of subiculum neurons in a mouse model of SCN8A epileptic encephalopathy.
    Wengert ER; Saga AU; Panchal PS; Barker BS; Patel MK
    Neuropharmacology; 2019 Nov; 158():107699. PubMed ID: 31278928
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The novel sodium channel modulator GS-458967 (GS967) is an effective treatment in a mouse model of SCN8A encephalopathy.
    Baker EM; Thompson CH; Hawkins NA; Wagnon JL; Wengert ER; Patel MK; George AL; Meisler MH; Kearney JA
    Epilepsia; 2018 Jun; 59(6):1166-1176. PubMed ID: 29782051
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathy.
    Estacion M; O'Brien JE; Conravey A; Hammer MF; Waxman SG; Dib-Hajj SD; Meisler MH
    Neurobiol Dis; 2014 Sep; 69():117-23. PubMed ID: 24874546
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. The SCN8A encephalopathy mutation p.Ile1327Val displays elevated sensitivity to the anticonvulsant phenytoin.
    Barker BS; Ottolini M; Wagnon JL; Hollander RM; Meisler MH; Patel MK
    Epilepsia; 2016 Sep; 57(9):1458-66. PubMed ID: 27375106
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variant-specific changes in persistent or resurgent sodium current in SCN8A-related epilepsy patient-derived neurons.
    Tidball AM; Lopez-Santiago LF; Yuan Y; Glenn TW; Margolis JL; Clayton Walker J; Kilbane EG; Miller CA; Martina Bebin E; Scott Perry M; Isom LL; Parent JM
    Brain; 2020 Oct; 143(10):3025-3040. PubMed ID: 32968789
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report.
    Lin KM; Su G; Wang F; Zhang X; Wang Y; Ren J; Wang X; Yao Y; Zhou Y
    BMC Pediatr; 2019 Nov; 19(1):400. PubMed ID: 31672125
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early onset epileptic encephalopathy caused by de novo SCN8A mutations.
    Ohba C; Kato M; Takahashi S; Lerman-Sagie T; Lev D; Terashima H; Kubota M; Kawawaki H; Matsufuji M; Kojima Y; Tateno A; Goldberg-Stern H; Straussberg R; Marom D; Leshinsky-Silver E; Nakashima M; Nishiyama K; Tsurusaki Y; Miyake N; Tanaka F; Matsumoto N; Saitsu H
    Epilepsia; 2014 Jul; 55(7):994-1000. PubMed ID: 24888894
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SCN8A encephalopathy: Mechanisms and models.
    Meisler MH
    Epilepsia; 2019 Dec; 60 Suppl 3(Suppl 3):S86-S91. PubMed ID: 31904118
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SCN8A encephalopathy: Research progress and prospects.
    Meisler MH; Helman G; Hammer MF; Fureman BE; Gaillard WD; Goldin AL; Hirose S; Ishii A; Kroner BL; Lossin C; Mefford HC; Parent JM; Patel M; Schreiber J; Stewart R; Whittemore V; Wilcox K; Wagnon JL; Pearl PL; Vanderver A; Scheffer IE
    Epilepsia; 2016 Jul; 57(7):1027-35. PubMed ID: 27270488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The phenotypic spectrum of SCN8A encephalopathy.
    Larsen J; Carvill GL; Gardella E; Kluger G; Schmiedel G; Barisic N; Depienne C; Brilstra E; Mang Y; Nielsen JE; Kirkpatrick M; Goudie D; Goldman R; Jähn JA; Jepsen B; Gill D; Döcker M; Biskup S; McMahon JM; Koeleman B; Harris M; Braun K; de Kovel CG; Marini C; Specchio N; Djémié T; Weckhuysen S; Tommerup N; Troncoso M; Troncoso L; Bevot A; Wolff M; Hjalgrim H; Guerrini R; Scheffer IE; Mefford HC; Møller RS;
    Neurology; 2015 Feb; 84(5):480-9. PubMed ID: 25568300
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distinct functional alterations in SCN8A epilepsy mutant channels.
    Pan Y; Cummins TR
    J Physiol; 2020 Jan; 598(2):381-401. PubMed ID: 31715021
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SCN8A Epilepsy, Developmental Encephalopathy, and Related Disorders.
    Talwar D; Hammer MF
    Pediatr Neurol; 2021 Sep; 122():76-83. PubMed ID: 34353676
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.