BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 20647993)

  • 1. Genetic evaluation and counseling for epilepsy.
    Pal DK; Pong AW; Chung WK
    Nat Rev Neurol; 2010 Aug; 6(8):445-53. PubMed ID: 20647993
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic testing in the epilepsies-developments and dilemmas.
    Poduri A; Sheidley BR; Shostak S; Ottman R
    Nat Rev Neurol; 2014 May; 10(5):293-9. PubMed ID: 24733164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic testing for kidney disease of unknown etiology.
    Hays T; Groopman EE; Gharavi AG
    Kidney Int; 2020 Sep; 98(3):590-600. PubMed ID: 32739203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Patients' understanding of and responses to multiplex genetic susceptibility test results.
    Kaphingst KA; McBride CM; Wade C; Alford SH; Reid R; Larson E; Baxevanis AD; Brody LC
    Genet Med; 2012 Jul; 14(7):681-7. PubMed ID: 22481132
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic testing for unexplained epilepsy: A review of diagnostic approach, benefits, and referral algorithm.
    Karlin A; Ruggiero S; Fitzgerald M
    Curr Probl Pediatr Adolesc Health Care; 2024 Mar; ():101579. PubMed ID: 38480044
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Panel testing may not be sufficient to reveal the etiology of suspected genetic epilepsy.
    Finsterer J; Scorza FA
    Rev Assoc Med Bras (1992); 2024; 70(6):e20231570. PubMed ID: 38808894
    [No Abstract]   [Full Text] [Related]  

  • 7. Epilepsy-associated genes: discovery, clinical significance, and underlying principles of genetic medicine.
    Liao WP
    Seizure; 2024 Mar; 116():1-3. PubMed ID: 38245481
    [No Abstract]   [Full Text] [Related]  

  • 8. Epilepsy and genetics.
    Lemke JR
    Med Genet; 2022 Oct; 34(3):199-200. PubMed ID: 38835871
    [No Abstract]   [Full Text] [Related]  

  • 9. Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist.
    Pong AW; Pal DK; Chung WK
    Pediatr Neurol; 2011 May; 44(5):317-27. PubMed ID: 21481738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
    Scheffer IE; Berkovic S; Capovilla G; Connolly MB; French J; Guilhoto L; Hirsch E; Jain S; Mathern GW; Moshé SL; Nordli DR; Perucca E; Tomson T; Wiebe S; Zhang YH; Zuberi SM
    Epilepsia; 2017 Apr; 58(4):512-521. PubMed ID: 28276062
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy.
    Truty R; Patil N; Sankar R; Sullivan J; Millichap J; Carvill G; Entezam A; Esplin ED; Fuller A; Hogue M; Johnson B; Khouzam A; Kobayashi Y; Lewis R; Nykamp K; Riethmaier D; Westbrook J; Zeman M; Nussbaum RL; Aradhya S
    Epilepsia Open; 2019 Sep; 4(3):397-408. PubMed ID: 31440721
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epigenetics in epilepsy.
    Kobow K; Blümcke I
    Neurosci Lett; 2018 Feb; 667():40-46. PubMed ID: 28111355
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
    Helbig KL; Farwell Hagman KD; Shinde DN; Mroske C; Powis Z; Li S; Tang S; Helbig I
    Genet Med; 2016 Sep; 18(9):898-905. PubMed ID: 26795593
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Epilepsy-associated genes.
    Wang J; Lin ZJ; Liu L; Xu HQ; Shi YW; Yi YH; He N; Liao WP
    Seizure; 2017 Jan; 44():11-20. PubMed ID: 28007376
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.
    Bayat A; Bayat M; Rubboli G; Møller RS
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356067
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Changing Times for CLN2 Disease: The Era of Enzyme Replacement Therapy.
    Specchio N; Pietrafusa N; Trivisano M
    Ther Clin Risk Manag; 2020; 16():213-222. PubMed ID: 32280231
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epilepsy genetics: Current knowledge, applications, and future directions.
    Myers KA; Johnstone DL; Dyment DA
    Clin Genet; 2019 Jan; 95(1):95-111. PubMed ID: 29992546
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital.
    Bashiri FA; AlSheikh R; Hamad MH; Alsheikh H; Alsheikh RA; Kentab A; AlTheeb N; Alghamdi M
    Children (Basel); 2023 Aug; 10(8):. PubMed ID: 37628333
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of the ADORA2A receptor and CD73 polymorphisms with epilepsy.
    Shi NR; Wang Q; Liu J; Zhang JZ; Deng BL; Hu XM; Yang J; Wang X; Chen X; Zuo YQ; Liu TT; Zheng JL; Yang X; Illes P; Tang Y
    Front Pharmacol; 2023; 14():1152667. PubMed ID: 37063258
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel
    Wang S; Cai X; Liu S; Zhou Q; Wang T; Du S; Wang D; Yang F; Wu Q; Han Y
    Front Mol Neurosci; 2022; 15():1010101. PubMed ID: 36568279
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.