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 *

157 related articles for article (PubMed ID: 34579535)

  • 1. Precision Medicine Approaches for Infantile-Onset Developmental and Epileptic Encephalopathies.
    Myers KA; Scheffer IE
    Annu Rev Pharmacol Toxicol; 2022 Jan; 62():641-662. PubMed ID: 34579535
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children.
    Elkhateeb N; Issa MY; Elbendary HM; Elnaggar W; Ramadan A; Rafat K; Kamel M; Abdel-Ghafar SF; Amer F; Hassaan HM; Trunzo R; Pereira C; Abdel-Hamid MS; D'Arco F; Bauer P; Bertoli-Avella AM; Girgis M; Gleeson JG; Zaki MS; Selim L
    Clin Genet; 2024 May; 105(5):510-522. PubMed ID: 38221827
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Developmental and epileptic encephalopathies: recognition and approaches to care.
    Raga S; Specchio N; Rheims S; Wilmshurst JM
    Epileptic Disord; 2021 Feb; 23(1):40-52. PubMed ID: 33632673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Epilepsy surgery in developmental and epileptic encephalopathies.
    Ramantani G; Wirrell E
    Epilepsy Behav; 2024 Oct; 159():109985. PubMed ID: 39181112
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Precision medicine for developmental and epileptic encephalopathies in Africa-strategies for a resource-limited setting.
    Esterhuizen AI; Tiffin N; Riordan G; Wessels M; Burman RJ; Aziz MC; Calhoun JD; Gunti J; Amiri EE; Ramamurthy A; Bamshad MJ; ; Mefford HC; Ramesar R; Wilmshurst JM; Carvill GL
    Genet Med; 2023 Feb; 25(2):100333. PubMed ID: 36480001
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. What are the epileptic encephalopathies?
    Trivisano M; Specchio N
    Curr Opin Neurol; 2020 Apr; 33(2):179-184. PubMed ID: 32049741
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Metabolic causes of pediatric developmental & epileptic encephalopathies (DEE)- genetic variant analysis in a south Indian cohort.
    Jose M; Fasaludeen A; Pavuluri H; Rudrabhatla PK; Chandrasekharan SV; Jose J; Banerjee M; Sundaram S; Radhakrishnan A; Menon RN
    Seizure; 2024 Feb; 115():20-27. PubMed ID: 38183824
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Treatment of Epileptic Encephalopathies.
    Balestrini S; Sisodiya SM
    Curr Pharm Des; 2017; 23(37):5667-5690. PubMed ID: 28799511
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Early-Onset Developmental and Epileptic Encephalopathies of Infancy: An Overview of the Genetic Basis and Clinical Features.
    Morrison-Levy N; Borlot F; Jain P; Whitney R
    Pediatr Neurol; 2021 Mar; 116():85-94. PubMed ID: 33515866
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome.
    Bar C; Kuchenbuch M; Barcia G; Schneider A; Jennesson M; Le Guyader G; Lesca G; Mignot C; Montomoli M; Parrini E; Isnard H; Rolland A; Keren B; Afenjar A; Dorison N; Sadleir LG; Breuillard D; Levy R; Rio M; Dupont S; Negrin S; Danieli A; Scalais E; De Saint Martin A; El Chehadeh S; Chelly J; Poisson A; Lebre AS; Nica A; Odent S; Sekhara T; Brankovic V; Goldenberg A; Vrielynck P; Lederer D; Maurey H; Terrone G; Besmond C; Hubert L; Berquin P; Billette de Villemeur T; Isidor B; Freeman JL; Mefford HC; Myers CT; Howell KB; Rodríguez-Sacristán Cascajo A; Meyer P; Genevieve D; Guët A; Doummar D; Durigneux J; van Dooren MF; de Wit MCY; Gerard M; Marey I; Munnich A; Guerrini R; Scheffer IE; Kabashi E; Nabbout R
    Epilepsia; 2020 Nov; 61(11):2461-2473. PubMed ID: 32954514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Long-term course of early onset developmental and epileptic encephalopathy associated with 2q24.3 microduplication.
    Masuda T; Osaka H; Tsuchida N; Miyatake S; Nishimura K; Takenouchi T; Takahashi T; Matsumoto N; Yamagata T
    Epilepsy Behav Rep; 2022; 19():100547. PubMed ID: 35733834
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability.
    Schneider AL; Myers CT; Muir AM; Calvert S; Basinger A; Perry MS; Rodan L; Helbig KL; Chambers C; Gorman KM; King MD; Donkervoort S; Soldatos A; Bönnemann CG; Spataro N; Gabau E; Arellano M; Cappuccio G; Brunetti-Pierri N; Rossignol E; Hamdan FF; Michaud JL; Balak C; Mefford HC; Scheffer IE
    Epilepsia; 2021 Jan; 62(1):e13-e21. PubMed ID: 33280099
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The phenotype and treatment of SCN2A-related developmental and epileptic encephalopathy.
    Kim HJ; Yang D; Kim SH; Kim B; Kim HD; Lee JS; Choi JR; Lee ST; Kang HC
    Epileptic Disord; 2020 Oct; 22(5):563-570. PubMed ID: 33000761
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.