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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

235 related items for PubMed ID: 33827760

  • 21. Global modified-Delphi consensus on comorbidities and prognosis of SCN8A-related epilepsy and/or neurodevelopmental disorders.
    Conecker G, Xia MY, Hecker J, Achkar C, Cukiert C, Devries S, Donner E, Fitzgerald M, Gardella E, Hammer M, Hegde A, Hu C, Kato M, Luo T, Schreiber JM, Wang Y, Kooistra T, Oudin M, Waldrop K, Youngquist JT, Zhang D, Wirrell E, Perry MS.
    Epilepsia; 2024 Aug; 65(8):2308-2321. PubMed ID: 38802989
    [Abstract] [Full Text] [Related]

  • 22. Ictal asystole: a case presentation.
    Kishk N, Nawito A, El-Damaty A, Ragab A.
    BMC Neurol; 2018 Jul 21; 18(1):100. PubMed ID: 30031379
    [Abstract] [Full Text] [Related]

  • 23. 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 21; 57(9):1458-66. PubMed ID: 27375106
    [Abstract] [Full Text] [Related]

  • 24. Paroxysmal tonic upgaze in a child with SCN8A-related encephalopathy.
    Solazzi R, Castellotti B, Canafoglia L, Messina G, Magri S, Freri E, Ragona F, Franceschetti S, Di Francesco JC, Gellera C, Granata T.
    Epileptic Disord; 2021 Aug 01; 23(4):643-647. PubMed ID: 34259158
    [Abstract] [Full Text] [Related]

  • 25. SCN8A Epilepsy, Developmental Encephalopathy, and Related Disorders.
    Talwar D, Hammer MF.
    Pediatr Neurol; 2021 Sep 01; 122():76-83. PubMed ID: 34353676
    [Abstract] [Full Text] [Related]

  • 26. Clinical study of 19 patients with SCN8A-related epilepsy: Two modes of onset regarding EEG and seizures.
    Denis J, Villeneuve N, Cacciagli P, Mignon-Ravix C, Lacoste C, Lefranc J, Napuri S, Damaj L, Villega F, Pedespan JM, Moutton S, Mignot C, Doummar D, Lion-François L, Gataullina S, Dulac O, Martin M, Gueden S, Lesca G, Julia S, Cances C, Journel H, Altuzarra C, Ben Zeev B, Afenjar A, Barth M, Villard L, Milh M.
    Epilepsia; 2019 May 01; 60(5):845-856. PubMed ID: 31026061
    [Abstract] [Full Text] [Related]

  • 27. Beyond the Norm: A Report of a Rare Case of Sodium Channel 8 Alpha (SCN8A) Gene-Related Epilepsy Unveiled in a Nine-Year-Old Child.
    K SSNSP, Vagha K, Varma A, Javvaji CK, Bhanushali K, Malik A, Handargule A.
    Cureus; 2024 May 01; 16(5):e59775. PubMed ID: 38846250
    [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 01; 158():106222. PubMed ID: 31675620
    [Abstract] [Full Text] [Related]

  • 29. Syncope, Epilepsy and Ictal Asystole: A Case Series and Narrative Review.
    Sowden N, Booth C, Kaye G.
    Heart Lung Circ; 2022 Jan 01; 31(1):25-31. PubMed ID: 34366218
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Ictal cardiorespiratory depression: a real risk for sudden unexpected death in epilepsy (SUDEP)?
    Pasini E, Provini F, Michelucci R.
    BMJ Case Rep; 2018 Aug 23; 2018():. PubMed ID: 30139784
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No 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 23; 7(2):280-292. PubMed ID: 34826216
    [Abstract] [Full Text] [Related]

  • 37. 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 23; 29(12):NP202-6. PubMed ID: 24352161
    [Abstract] [Full Text] [Related]

  • 38. The spectrum of intermediate SCN8A-related epilepsy.
    Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS.
    Epilepsia; 2019 May 23; 60(5):830-844. PubMed ID: 30968951
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.