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.


Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 37176165)

  • 1. GABA
    Nwosu GI; Shen W; Zavalin K; Poliquin S; Randhave K; Flamm C; Biven M; Langer K; Kang JQ
    Int J Mol Sci; 2023 May; 24(9):. PubMed ID: 37176165
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes.
    Shi YW; Zhang Q; Cai K; Poliquin S; Shen W; Winters N; Yi YH; Wang J; Hu N; Macdonald RL; Liao WP; Kang JQ
    Brain; 2019 Oct; 142(10):3028-3044. PubMed ID: 31435640
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GABA
    Qu S; Catron M; Zhou C; Janve V; Shen W; Howe RK; Macdonald RL
    Brain Commun; 2020; 2(1):fcaa028. PubMed ID: 32467926
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heterozygous GABA
    Qu S; Jackson LG; Zhou C; Shen D; Shen W; Nwosu G; Howe R; Catron MA; Flamm C; Biven M; Kang JQ; Macdonald RL
    Epilepsia; 2023 Apr; 64(4):1061-1073. PubMed ID: 36495145
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy.
    Papandreou A; McTague A; Trump N; Ambegaonkar G; Ngoh A; Meyer E; Scott RH; Kurian MA
    Dev Med Child Neurol; 2016 Apr; 58(4):416-20. PubMed ID: 26645412
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Asymmetric Slow-Spike-Wave Patterns with Maximal Discharges Contralateral to MRI Lesions Predict Better Surgical Prognosis in Symptomatic Lennox-Gastaut Syndrome or Lennox-Gastaut Phenotypes.
    Yang MH; Liu J; Zhou YL; Yang H; Cai FC; Zempel J; Yang QW; Liu SY
    Pediatr Neurosurg; 2020; 55(1):26-35. PubMed ID: 31851997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man.
    DeLorey TM; Olsen RW
    Epilepsy Res; 1999 Sep; 36(2-3):123-32. PubMed ID: 10515160
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort study.
    Nightscales R; Chen Z; Barnard S; Auvrez C; Tao G; Sivathamboo S; Bennett C; Rychkova M; D'Souza W; Berkovic SF; Nicolo JP; O'Brien TJ; Perucca P; Scheffer IE; Kwan P
    Epilepsia Open; 2024 Apr; 9(2):602-612. PubMed ID: 38135919
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Understanding Lennox-Gastaut syndrome: insights from focal epilepsy patients with Lennox-Gastaut features.
    Dupont S; Banica-Wolters R; An-Gourfinkel I; Lambrecq V; Navarro V; Adam C; Nguyen-Michel VH
    J Neurol; 2017 Jul; 264(7):1388-1396. PubMed ID: 28584915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expert opinion: Proposed diagnostic and treatment algorithms for Lennox-Gastaut syndrome in adult patients.
    Montouris G; Aboumatar S; Burdette D; Kothare S; Kuzniecky R; Rosenfeld W; Chung S
    Epilepsy Behav; 2020 Sep; 110():107146. PubMed ID: 32563898
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lennox Gastaut Syndrome - A strategic shift in diagnosis over time?
    Evans NJ; Das K
    Seizure; 2022 Dec; 103():68-71. PubMed ID: 36332460
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epileptic encephalopathy de novo GABRB mutations impair γ-aminobutyric acid type A receptor function.
    Janve VS; Hernandez CC; Verdier KM; Hu N; Macdonald RL
    Ann Neurol; 2016 May; 79(5):806-825. PubMed ID: 26950270
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Correlations of receptor desensitization of gain-of-function GABRB3 variants with clinical severity.
    Lin SXN; Ahring PK; Keramidas A; Liao VWY; Møller RS; Chebib M; Absalom NL
    Brain; 2024 Jan; 147(1):224-239. PubMed ID: 37647766
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CHD2 mutations in Lennox-Gastaut syndrome.
    Lund C; Brodtkorb E; Øye AM; Røsby O; Selmer KK
    Epilepsy Behav; 2014 Apr; 33():18-21. PubMed ID: 24614520
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cleft Palate as Distinguishing Feature in a Patient with GABRB3 Epileptic Encephalopathy.
    Bamborschke D; Pergande M; Daimagüler HS; Mangold E; Dötsch J; Herkenrath P; Cirak S; Fazeli W
    Neuropediatrics; 2019 Dec; 50(6):378-381. PubMed ID: 31319422
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.
    DeLorey TM; Handforth A; Anagnostaras SG; Homanics GE; Minassian BA; Asatourian A; Fanselow MS; Delgado-Escueta A; Ellison GD; Olsen RW
    J Neurosci; 1998 Oct; 18(20):8505-14. PubMed ID: 9763493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evolution and course of early life developmental encephalopathic epilepsies: Focus on Lennox-Gastaut syndrome.
    Berg AT; Levy SR; Testa FM
    Epilepsia; 2018 Nov; 59(11):2096-2105. PubMed ID: 30255934
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early onset epileptic encephalopathy with a novel GABRB3 mutation treated effectively with clonazepam: A case report.
    Zhang Y; Lian Y; Xie N
    Medicine (Baltimore); 2017 Dec; 96(50):e9273. PubMed ID: 29390378
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The unchanging face of Lennox-Gastaut syndrome in adulthood.
    Reyhani A; Özkara Ç
    Epilepsy Res; 2021 May; 172():106575. PubMed ID: 33721709
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lennox-Gastaut syndrome: a comprehensive review.
    Asadi-Pooya AA
    Neurol Sci; 2018 Mar; 39(3):403-414. PubMed ID: 29124439
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.