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 *

253 related articles for article (PubMed ID: 33349540)

  • 21. GABRG1 variant as a potential novel cause of epileptic encephalopathy, hypotonia, and global developmental delay.
    Williams A; Cooney E; Segal G; Narayanan S; Morand M; Agadi S
    Am J Med Genet A; 2022 Dec; 188(12):3546-3549. PubMed ID: 36121006
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The spectrum of SCN1A-related infantile epileptic encephalopathies.
    Harkin LA; McMahon JM; Iona X; Dibbens L; Pelekanos JT; Zuberi SM; Sadleir LG; Andermann E; Gill D; Farrell K; Connolly M; Stanley T; Harbord M; Andermann F; Wang J; Batish SD; Jones JG; Seltzer WK; Gardner A; ; Sutherland G; Berkovic SF; Mulley JC; Scheffer IE
    Brain; 2007 Mar; 130(Pt 3):843-52. PubMed ID: 17347258
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Genotype and phenotype of children with KCNA2 gene related developmental and epileptic encephalopathy].
    Gong P; Xue J; Jiao XR; Zhang YH; Yang ZX
    Zhonghua Er Ke Za Zhi; 2020 Jan; 58(1):35-40. PubMed ID: 31905474
    [No Abstract]   [Full Text] [Related]  

  • 24. Cohort of Phenotype, Genotype, and Outcome of
    Gowda VK; Battina M; Vegda H; Srinivasan VM; Chikara SK; Mishra A; Shivappa SK; Benakappa N
    J Pediatr Genet; 2023 Mar; 12(1):32-41. PubMed ID: 36684540
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Comparative analysis of prognostic value of epileptic encephalopathies and symptomatic epilepsy in children with cerebral palsy].
    Kakushadze ZN; Bokeriia IR; Natroshvili IG; Kandareli LG; Davituliani KhR
    Georgian Med News; 2005 Nov; (128):66-9. PubMed ID: 16369069
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Neonatal Developmental and Epileptic Encephalopathies.
    El Kosseifi C; Cornet MC; Cilio MR
    Semin Pediatr Neurol; 2019 Dec; 32():100770. PubMed ID: 31813518
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Treatment of epileptic encephalopathies.
    McTague A; Cross JH
    CNS Drugs; 2013 Mar; 27(3):175-84. PubMed ID: 23397290
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Epileptic encephalopathies and progressive neurodegeneration.
    Guerrini R; Conti V
    Rev Neurol (Paris); 2024 May; 180(5):363-367. PubMed ID: 38582661
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Multiple independent spike foci and epilepsy, with special reference to a new epileptic syndrome of "severe epilepsy with multiple independent spike foci".
    Yamatogi Y; Ohtahara S
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S96-104. PubMed ID: 16829042
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Insights from Spatial Measures of Intolerance to Identifying Pathogenic Variants in Developmental and Epileptic Encephalopathies.
    Silk M; de Sá A; Olshansky M; Ascher DB
    Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36982187
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Before the first seizure: The developmental imprint of infant epilepsy on neurodevelopment.
    Milh M
    Rev Neurol (Paris); 2023 Apr; 179(4):330-336. PubMed ID: 36907712
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Atypical absence seizures and gene variants: A gene-based review of etiology, electro-clinical features, and associated epilepsy syndrome.
    Zhao X; He Z; Li Y; Yang X; Li B
    Epilepsy Behav; 2024 Feb; 151():109636. PubMed ID: 38232560
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Epileptic Encephalopathies of Childhood: The New Paradigm of Genetic Diagnosis].
    Martins R; Moldovan O; Sousa AB; Levy A; Quintas S
    Acta Med Port; 2020 Jun; 33(6):415-424. PubMed ID: 32504517
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Nonconvulsive status epilepticus in epileptic encephalopathies in childhood.
    Hamad AP; Ferrari-Marinho T; Caboclo LO; Thomé U; Fernandes RMF
    Seizure; 2020 Aug; 80():212-220. PubMed ID: 32645639
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical review of genetic epileptic encephalopathies.
    Noh GJ; Jane Tavyev Asher Y; Graham JM
    Eur J Med Genet; 2012 May; 55(5):281-98. PubMed ID: 22342633
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Natural History Studies and Clinical Trial Readiness for Genetic Developmental and Epileptic Encephalopathies.
    Palmer EE; Howell K; Scheffer IE
    Neurotherapeutics; 2021 Jul; 18(3):1432-1444. PubMed ID: 34708325
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic Epilepsy Syndromes.
    Myers KA
    Continuum (Minneap Minn); 2022 Apr; 28(2):339-362. PubMed ID: 35393962
    [TBL] [Abstract][Full Text] [Related]  

  • 38. New paradigms for the treatment of pediatric monogenic epilepsies: Progressing toward precision medicine.
    Specchio N; Pietrafusa N; Perucca E; Cross JH
    Epilepsy Behav; 2022 Jun; 131(Pt B):107961. PubMed ID: 33867301
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Epilepsy Surgery for Cognitive Improvement in Epileptic Encephalopathy.
    McLaren JR; Kahle KT; Richardson RM; Chu CJ
    Neurosurg Clin N Am; 2024 Jan; 35(1):49-59. PubMed ID: 38000841
    [TBL] [Abstract][Full Text] [Related]  

  • 40. What are the considerations when initiating treatment for epilepsy in children?
    Pisani F; Spagnoli C
    Expert Rev Neurother; 2023; 23(12):1081-1096. PubMed ID: 38032395
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.