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 *

319 related articles for article (PubMed ID: 26073591)

  • 1. Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes.
    Mastrangelo M
    Pediatr Neurol; 2015 Aug; 53(2):119-29. PubMed ID: 26073591
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy.
    Na JH; Shin S; Yang D; Kim B; Kim HD; Kim S; Lee JS; Choi JR; Lee ST; Kang HC
    Brain Dev; 2020 Jun; 42(6):438-448. PubMed ID: 32139178
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.
    Allen NM; Conroy J; Shahwan A; Lynch B; Correa RG; Pena SD; McCreary D; Magalhães TR; Ennis S; Lynch SA; King MD
    Epilepsia; 2016 Jan; 57(1):e12-7. PubMed ID: 26648591
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies.
    He N; Lin ZJ; Wang J; Wei F; Meng H; Liu XR; Chen Q; Su T; Shi YW; Yi YH; Liao WP
    Genet Med; 2019 Jan; 21(1):17-27. PubMed ID: 29895856
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnostic yield of genetic testing in epileptic encephalopathy in childhood.
    Mercimek-Mahmutoglu S; Patel J; Cordeiro D; Hewson S; Callen D; Donner EJ; Hahn CD; Kannu P; Kobayashi J; Minassian BA; Moharir M; Siriwardena K; Weiss SK; Weksberg R; Snead OC
    Epilepsia; 2015 May; 56(5):707-16. PubMed ID: 25818041
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Infantile epileptic encephalopathies: what matters is genetics].
    Garcia-Penas JJ; Jimenez-Legido M
    Rev Neurol; 2017 May; 64(s03):S65-S69. PubMed ID: 28524223
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype correlates of infantile-onset developmental & epileptic encephalopathy syndromes in South India: A single centre experience.
    Mitta N; Menon RN; McTague A; Radhakrishnan A; Sundaram S; Cherian A; Madhavilatha GK; Mannan AU; Nampoothiri S; Thomas SV
    Epilepsy Res; 2020 Oct; 166():106398. PubMed ID: 32593896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders.
    Kobayashi Y; Tohyama J; Kato M; Akasaka N; Magara S; Kawashima H; Ohashi T; Shiraishi H; Nakashima M; Saitsu H; Matsumoto N
    Brain Dev; 2016 Mar; 38(3):285-92. PubMed ID: 26482601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
    Gerald B; Ramsey K; Belnap N; Szelinger S; Siniard AL; Balak C; Russell M; Richholt R; De Both M; Claasen AM; Schrauwen I; Huentelman MJ; Craig DW; Rangasamy S; Narayanan V
    Semin Pediatr Neurol; 2018 Jul; 26():28-32. PubMed ID: 29961512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
    Arnadottir GA; Jensson BO; Marelsson SE; Sulem G; Oddsson A; Kristjansson RP; Benonisdottir S; Gudjonsson SA; Masson G; Thorisson GA; Saemundsdottir J; Magnusson OT; Jonasdottir A; Jonasdottir A; Sigurdsson A; Gudbjartsson DF; Thorsteinsdottir U; Arngrimsson R; Sulem P; Stefansson K
    BMC Med Genet; 2017 Oct; 18(1):103. PubMed ID: 28965491
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Epileptic encephalopathies in infants and children.
    Nordli DR
    J Clin Neurophysiol; 2012 Oct; 29(5):420-4. PubMed ID: 23027099
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genes of early-onset epileptic encephalopathies: from genotype to phenotype.
    Mastrangelo M; Leuzzi V
    Pediatr Neurol; 2012 Jan; 46(1):24-31. PubMed ID: 22196487
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Early epileptic encephalopathies associated with STXBP1 mutations: Could we better delineate the phenotype?
    Barcia G; Chemaly N; Gobin S; Milh M; Van Bogaert P; Barnerias C; Kaminska A; Dulac O; Desguerre I; Cormier V; Boddaert N; Nabbout R
    Eur J Med Genet; 2014 Jan; 57(1):15-20. PubMed ID: 24189369
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.
    Olson HE; Kelly M; LaCoursiere CM; Pinsky R; Tambunan D; Shain C; Ramgopal S; Takeoka M; Libenson MH; Julich K; Loddenkemper T; Marsh ED; Segal D; Koh S; Salman MS; Paciorkowski AR; Yang E; Bergin AM; Sheidley BR; Poduri A
    Ann Neurol; 2017 Mar; 81(3):419-429. PubMed ID: 28133863
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy.
    Gokben S; Onay H; Yilmaz S; Atik T; Serdaroglu G; Tekin H; Ozkinay F
    Acta Neurol Belg; 2017 Mar; 117(1):131-138. PubMed ID: 27734276
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2].
    Terczyńska I; Mierzewska H; Szczepanik E; Antczak-Marach D
    Przegl Lek; 2010; 67(9):757-61. PubMed ID: 21387820
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.
    Heron SE; Ong YS; Yendle SC; McMahon JM; Berkovic SF; Scheffer IE; Dibbens LM
    Epilepsia; 2013 May; 54(5):e86-9. PubMed ID: 23566103
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.