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 *

308 related articles for article (PubMed ID: 36571524)

  • 21. Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy.
    Gürsoy S; Erçal D
    J Child Neurol; 2016 Mar; 31(4):523-32. PubMed ID: 26271793
    [TBL] [Abstract][Full Text] [Related]  

  • 22. SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy.
    Zhu Z; Bolt E; Newmaster K; Osei-Bonsu W; Cohen S; Cuddapah VA; Gupta S; Paudel S; Samanta D; Dang LT; Carney PR; Naik S
    Children (Basel); 2022 Oct; 9(10):. PubMed ID: 36291443
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A retrospective study of the yield of next-generation sequencing in the diagnosis of developmental and epileptic encephalopathies and epileptic encephalopathies in 0-12 years aged children at a single tertiary care hospital in South India.
    Murthy MC; Banerjee B; Shetty M; Mariappan M; Sekhsaria A
    Epileptic Disord; 2024 Oct; 26(5):609-625. PubMed ID: 38923778
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nonseizure consequences of Dravet syndrome, KCNQ2-DEE, KCNB1-DEE, Lennox-Gastaut syndrome, ESES: A functional framework.
    Berg AT; Gaebler-Spira D; Wilkening G; Zelko F; Knupp K; Dixon-Salazar T; Villas N; Meskis MA; Harwell V; Thompson T; Sims S; Nesbitt G
    Epilepsy Behav; 2020 Oct; 111():107287. PubMed ID: 32759067
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Epileptic encephalopathies: new genes and new pathways.
    Nieh SE; Sherr EH
    Neurotherapeutics; 2014 Oct; 11(4):796-806. PubMed ID: 25266964
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome.
    He N; Li BM; Li ZX; Wang J; Liu XR; Meng H; Tang B; Bian WJ; Shi YW; Liao WP
    J Neurodev Disord; 2018 Mar; 10(1):10. PubMed ID: 29558884
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy.
    Ko A; Youn SE; Kim SH; Lee JS; Kim S; Choi JR; Kim HD; Lee ST; Kang HC
    Epilepsy Res; 2018 Mar; 141():48-55. PubMed ID: 29455050
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Lennox-Gastaut syndrome (childhood epileptic encephalopathy).
    Markand ON
    J Clin Neurophysiol; 2003; 20(6):426-41. PubMed ID: 14734932
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features.
    Aljaafari D; Fasano A; Nascimento FA; Lang AE; Andrade DM
    Epilepsia; 2017 Mar; 58(3):e44-e48. PubMed ID: 28186331
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Epileptic encephalopathy.
    Dulac O
    Epilepsia; 2001; 42 Suppl 3():23-6. PubMed ID: 11520318
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Diagnosis switching and outcomes in a cohort of patients with potential epilepsy with myoclonic-atonic seizures.
    Eschbach K; Moss A; Joshi C; Angione K; Smith G; Dempsey A; Juarez-Colunga E; Demarest ST
    Epilepsy Res; 2018 Nov; 147():95-101. PubMed ID: 30286391
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rates of Status Epilepticus and Sudden Unexplained Death in Epilepsy in People With Genetic Developmental and Epileptic Encephalopathies.
    Donnan AM; Schneider AL; Russ-Hall S; Churilov L; Scheffer IE
    Neurology; 2023 Apr; 100(16):e1712-e1722. PubMed ID: 36750385
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Boricua Founder Variant in
    Abdelmoumen I; Jimenez S; Valencia I; Melvin J; Legido A; Diaz-Diaz MM; Griffith C; Massingham LJ; Yelton M; Rodríguez-Hernández J; Schnur RE; Walsh LE; Cristancho AG; Bergqvist CA; McWalter K; Mathieson I; Belbin GM; Kenny EE; Ortiz-Gonzalez XR; Schneider MC
    J Child Neurol; 2021 Feb; 36(2):93-98. PubMed ID: 32928027
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes.
    de Lange IM; Koudijs MJ; van 't Slot R; Gunning B; Sonsma ACM; van Gemert LJJM; Mulder F; Carbo EC; van Kempen MJA; Verbeek NE; Nijman IJ; Ernst RF; Savelberg SMC; Knoers NVAM; Brilstra EH; Koeleman BPC
    Epilepsia; 2018 Mar; 59(3):690-703. PubMed ID: 29460957
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dravet syndrome and its mimics: Beyond SCN1A.
    Steel D; Symonds JD; Zuberi SM; Brunklaus A
    Epilepsia; 2017 Nov; 58(11):1807-1816. PubMed ID: 28880996
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Comprehensive scoping review of fenfluramine's role in managing generalized tonic-clonic seizures in developmental and epileptic encephalopathies.
    Gil-Nagel A; Cross JH; Devinsky O; Ceulemans B; Lagae L; Knupp K; Schoonjans AS; Ryvlin P; Thiele EA; Polega S; Lothe A; Nabbout R
    Epilepsia; 2024 Aug; 65(8):2186-2199. PubMed ID: 39030735
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC; Hwang H; Kim H; Chae JH; Choi J; Kim KJ; Hwang YS; Yum MS; Ko TS
    Epilepsy Res; 2015 Jan; 109():34-9. PubMed ID: 25524840
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Monoamine neurotransmitters in early epileptic encephalopathies: New insights into pathophysiology and therapy.
    Juliá-Palacios N; Molina-Anguita C; Sigatulina Bondarenko M; Cortès-Saladelafont E; Aparicio J; Cuadras D; Horvath G; Fons C; Artuch R; García-Cazorla À;
    Dev Med Child Neurol; 2022 Jul; 64(7):915-923. PubMed ID: 35833444
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Both gain-of-function and loss-of-function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox-Gastaut syndrome.
    Jiang X; Raju PK; D'Avanzo N; Lachance M; Pepin J; Dubeau F; Mitchell WG; Bello-Espinosa LE; Pierson TM; Minassian BA; Lacaille JC; Rossignol E
    Epilepsia; 2019 Sep; 60(9):1881-1894. PubMed ID: 31468518
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Population-based study of rare epilepsy incidence in a US urban population.
    Barbour K; Tian N; Yozawitz EG; Wolf S; McGoldrick PE; Sands TT; Nelson A; Basma N; Grinspan ZM
    Epilepsia; 2024 Aug; 65(8):2341-2353. PubMed ID: 38795333
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.